Theme: Drug safety Management {CME-CPD Accreditations Available}

Drug Safety 2023

Drug Safety 2023

We are excited to have you attend the 16th International Conference on Pharmaceutics and Drug Safety. We are thrilled to have the chance to host this conference. The conference will take place in London , United Kingdom on September 08-09, 2023. The conference will attract professionals, physicians, universities, students, notable figures, academics, scientists and business from all over the world. This conference will introduce the world to fresh views and new methods for exploring uncharted territory. By these conferences, medical and service organisations can spread a message of hope for the future of pharmaceutics and drug safety research.

We are hoping that this conference will be motivating, helpful, and significant for each and every one of you.

The "16th International Conference on Pharmaceutics and Drug Safety" will be held in London,United Kingdom, on September 08-09, 2023, and is open to all attendees from across the world.

Pharmaceutics conference will bring together major figures in the global pharmaceutics and Drug Safety industry  from the fields of Pharmacy epidemiology, data analytics, pharmacovigilance, and drug safety. Examine benefit-risk management tactics, patient-centric approaches, and the use of big data and AI in pharmacovigilance. Also, talk about how to deal with social media difficulties and international drug safety legislation.

With a focus on how to advance pharmacovigilance and pharmaceutics operations, the conference aims to close the communication gap between representatives from academic institutions, industry, and international regulatory agencies.

Pharmacovigilance is expanding quickly, and its advancement is having a huge impact on medical and pharmaceutical research. Our aim is to engage, evolve, and explore knowledge among academics and industry personnel. The major attendees will be addressing Pharmaceutics Pharmacovigilance, Drug Safety, Adverse Drug Reactions, etc. We cordially invite you to attend the "16th international conference on pharmaceutics and drug safety," which will be focusing on the theme "Drug safety Management." Join us at this conference on drug safety in 2023 as we bring together fundamental research and significant advancements by drawing world-renowned academics, professionals, and specialists.

Target Audience

Pharmacologist | Psychologist | Pharmacogenomics | Pharmacology | Licensed behaviour analyst | Licensed professional counsellor | Mental health professional | School counsellor & Social Worker | Resource Worker | Graduates, Postgraduates & PhD Scholars | Professors, Associate Professors, Assistant Professors | Peer Support Worker | Grief and Bereavement Therapist | Pharmaceutical Companies & Manufacturing Companies | Research Institutes and members | Neurologists | Neurosurgeons | Researchers

Why to attend


Our extensive online advertising attracts 30000+ users and 50000+ views to our library of abstracts, driving researchers and speakers to our conference.

Meet hundreds of like-minded experts leading the Drug Safety 2023 and share ideas.

All conference participants will have a different reason to participate in one-on-one meetings with eminent speakers and famous keynote speakers.

In our keynote sessions you will have a wonderful opportunity to hear what the world's experts are learning from the world's most influential researchers in the fields of pharmaceutics and drug safety

Drug Safety 2023 Intensive Conference Schedule, you'll gain experience and expertise in crafting strategic gifts that are worth its weight golfing, creating an impressive array of recognized such professionals.

Nomination for Best Poster Award.

Outstanding Young Researcher Award.

Benefits of group registration.

Benefits of Participation for Speaker

Worldwide appreciation of the research design.

Receive credit for professional development.

Explore the latest analysis.

Learn a transition beyond your area of ​​interest to learn more about new topics and studies away from your core theme of the Drug Safety 2023.

We have exclusive networking, learning and integration in a single package.

Benefits of Participation for the Delegate

Professional development - improving understanding and knowledge.

Attendance at conferences rejuvenates and energizes delegates.

Your participation in our conference will help with a new approach and ideology that can be used to broaden the results of businesses or industries.

Opportunities for the Drug Safety 2023 for researchers and experts in the same field to meet and exchange new ideas through a physical conference.

Benefits of Participation for the Sponsor / Exhibitor

Exposure to international environment will increase the chances of new companies.

Opportunity to showcase your company's latest technologies, new products or serve your business to a wide range of international participants.

Building a successful company takes a lot of time and also lot of effort and drive, so it's always good to have a network of the colleagues and associates who draw energy from individuals who share a similar drive and purpose.

Conferences in Drug Safety provide opportunities for greater focus and reflection that can help you take your company to the next step.

Benchmarking key organization plans.


Track 1: Analyses and Quality Control for Pharmaceuticals

The term "pharmaceutical analysis" refers to the study of drugs, both as bulk drug molecules and as pharmaceutical products (formulations)

Pharmaceutical Quality Assurance is essential to ensuring that medicines are produced and dispensed in a consistent, secure manner. This is essential to make sure that no one becomes ill or experiences an aggravation of their symptoms as a result of taking the medication. Research, development, manufacturing, and distribution are just a few of the many facets of pharmaceutical quality assurance (PQA) that potentially compromise the integrity of medical products. To continue to be lawful, medications must maintain a high level of quality. The reputation and standards of the companies they work for must also be upheld.

  • Quality Assurance and Control
  • Pharmaceutical quality assurance
  • Purpose of Pharmaceutical Analysis and Quality Assurance

Track 2: Biopharmaceuticals, Biomolecules, and Therapeutics

Any substance made from living things or containing elements of live things is referred to as a biologic medicine (biologic). Pharmaceuticals derived from humans, animals, or microorganisms under the general heading of "biologic drugs" are produced using biotechnology. Biologic drugs include, among other things, vaccines, blood and blood components, cells, allergies, genes, tissues, and recombinant proteins.

A jack-of-all-trades in the medical field, biomolecules are capable of doing everything. Asthma and multiple sclerosis can both be treated with them, and immunizations against the flu and polio can assist the body's own immunological defences by boosting them. They can also be used to diagnose and treat malignant disorders. In the pharmaceutical industry, new biomolecules are continuously being created: Specific antibodies, customised proteins, and nucleic acids — the basic building blocks of genetic material — are all viewed as potential therapeutic candidates.

Drug therapy products with an active ingredient obtained from a biological source are referred to as biotherapeutics, often known as biologicals. Nearly half of all new drugs approved in recent years have been biotherapeutics, a market section of the pharmaceutical industry that is expanding quickly.

  • Cancer Biotherapy Treatment
  • Patient Education for Biotherapy and Chemotherapy
  • Utilized Biological Response Modifiers
  • Treatment of Wounds Using Biotherapy
  • Nuclear medicine uses radiopharmaceuticals
  • Radiopharmaceutical diagnostics

Track 3:Biotechnology and Microbiology in Pharmaceuticals

Pharmaceutical microbiology is the term used to describe the application of microbiology in pharmaceutical and healthcare situations. It is a subfield of microbiology that acknowledges the tremendous diversity of microorganisms in the environment, which has a wide range of potential outcomes, some of which are advantageous and others which are destructive. It emphasises the importance of a variety of microbes and toxins (microbial byproducts like endotoxins and pyrogens) in pharmaceutical raw materials, finished products, intermediates, and pharmaceutical manufacturing environments, as well as microbiological control of pharmaceutical products and manufacturing environments.

Pharmaceutical biotechnology, which applies biotechnology ideas to drug discovery, is a vibrant and expanding field. Pharmaceutical biotechnology, which applies biotechnology ideas to drug discovery, is a vibrant and expanding field. Utilizing monoclonal antibodies or recombinant DNA technology, which involves the genetic modification of cells, the pharmaceutical biotechnology sector produces biotechnological goods.

  • Preventing the deterioration of pharmaceuticals
  • Environments under control for RDT in drug development
  • Bacterial resistance
  • Microbiology
  • Biological molecular
  • Biochemistry
  • Genetics

Track 4: Cellular Targeting and  subcellular Delivery

Effective medications target tumours, tissue damage, or low-toxic medications at the infection site. Targeted medicine distribution has become more important in the treatment of many illness situations because it increases the pharmacological effects of pharmaceuticals and reduces their negative side effects. Few targeted drug delivery systems can achieve high targeting efficiency after intravenous injection, despite the discovery of several surface indicators and targeting strategies. Cell-mediated drug-delivery targeting systems have drawn a lot of attention due to their enhanced therapeutic specificity and effectiveness in the treatment of the disease. Cell-based drug delivery systems have a wide range of potential biological uses, providing new insights into the therapeutic potential of our cells. Different therapy approaches can be made significantly more effective by intracellular administration of various medications, including DNA and drug carriers.

  • Nano-based medication delivery system
  • Designing and Targeting Drugs
  • System for Delivering a Specific Drug

Track 5: Delivery of Medicine via Inhalation

For the treatment of respiratory conditions like asthma and chronic obstructive pulmonary disease, inhalation therapy is frequently employed. Compared to other methods of administration, inhalation provides a number of benefits in the treatment of various illnesses. In recent decades, inhalation therapy has become more and more common. The most recommended way to administer drugs used to treat respiratory conditions like asthma and chronic obstructive lung disease is currently through inhalation (COPD). The route of inhalation for systemic pharmaceutical administration is also being researched in specific circumstances. Inhalation therapy for local treatment primarily aims to alleviate and/or prevent pulmonary symptoms, such as airway irritation and tightness.

  • The demand for inhaled medication delivery
  • Nebulized treatment innovation
  • Modern advancements in nebulizers
  • Development of MDIs without propellants
  • Medication distribution through aerosols
  • The difficulties with triple-combination inhalers
  • Imaging of the breathing function

Track 6: Development and Production of Pharmaceutical Products

Present-day pharmaceutical product development and manufacture involves a series of scale-ups, starting with small amounts of material for preliminary safety or clinical studies and moving on to a manufacturing facility to offer commercial supply. The production of pharmaceutical drugs is the focus of the pharmaceutical manufacturing sector of the industry. Product development is different in the pharmaceutical sector from other industries. Because the science and engineering of pharmaceutical product development is not as advanced as, say, that of the chemical industry, it is essentially empirical, laborious, and time and resource intensive. This is the main reason why the pharmaceutical manufacturing business is still behind, despite the billions of dollars that have been invested in production by the pharmaceutical industry.

  • Technology and tools for manufacturing
  • Modern manufacturing processes
  • Pharmacy, both commercial and physical
  • Technology in Pharmaceuticals
  • Pharmaceutical Containers

Track 7: Drug Delivery Technology and Vaccine Design

Vaccines are substances that are given to patients to elicit immunological reactions that lead to the production of antibodies (humoral) or cell-mediated responses that will aid them in fighting infectious pathogens or non-infectious illnesses like cancer. Immunology, protein design, and genetic delivery advancements have created previously unthinkable opportunities for vaccination concepts and delivery methods. Since they have the potential to provide answers to challenging targets where conventional approaches have failed, these next-generation vaccine design attempts are very intriguing. Because they do away with the need for booster doses and give long-term therapy in manageable dosages, vaccine medication delivery systems have been proved to be patient-friendly. Their use is further encouraged by the development of needle-free administration methods.

  • IImmunotherapy and vaccinations
  • New Drug Delivery Systems for Vaccines

Track 8: Drug Delivery Using Peptides and Proteins

A protein is a large molecule made composed of one or more amino acids arranged in a certain order. Drugs are delivered to their target locations of action with the help of proteins and peptides. Over the past twenty years, researchers have focused on a wide range of biopharmaceutical process development domains. The majority of therapeutic proteins have been studied, and issues with cell culture, purification, recovery, and fermentation have all been solved. Mass synthesis of a number of chemicals allowed for their widespread application in medical therapy thanks to the quick development of biotechnology and developments in peptide and protein chemistry. Although not always, proteins and peptides play a significant role as regulators in biological processes.

Track 9: Drug Research and Evaluation

The process of finding chemical compounds that have the potential to be therapeutic agents is referred to as drug discovery. Drug development refers to all processes that take a chemical from drug candidate (the result of the discovery phase) to a finished good that has been given the go-ahead for commercialization by the appropriate regulatory bodies. A major objective of drug development programmes is the discovery of novel molecular entities that might be helpful in the treatment of disorders that fall under the category of unmet medical needs.

Prior to choosing a candidate drug for clinical trials, the process of drug screening involves locating and improving promising pharmaceuticals. To assess the potential of biological extracts or molecules, bioactive compound screening uses a wide variety of analytical techniques. The tests may be carried out on the entire animal, in individual cells, or at the molecular level. Reverse pharmacology, also known as target-based drug discovery, and classic pharmacology, commonly referred to as phenotypic drug discovery, are two complementing methods for finding new drugs. Phenotypic drug discovery is the historical foundation of drug discovery.

  • Models for Drug Screening in Vitro
  • Medication design based on structure
  • High-Throughput Screening (HTS)

Track 10: Drug Safety

The pharmaceutical science pertaining to the "gathering, identification, assessment, monitoring, and prevention" of adverse effects with pharmaceutical goods is known as pharmacovigilance, commonly referred to as drug safety. The words "pharmacovigilance" and "pharmakon," both from the Greek for "drug," have similar etymological roots (Latin for to keep watch). As a result, pharmacovigilance places a lot of emphasis on adverse drug reactions (ADR), which are described as any noxious and unintended response to a drug, such as a lack of efficacy (the condition that this definition only applies with the doses normally used for the prophylaxis, diagnosis or therapy of disease, or for the modification of physiological disorder function was excluded with the latest amendment of the applicable legislation). Even in the absence of an adverse event, medication errors such as overdosing, drug addiction, misuse, and exposure to drugs while pregnant or nursing are of importance since they may result in a negative pharmacological reaction.

Track 11: Intellectual property rights and regulatory  issues

Regulatory affairs is a field that keeps an eye on how foods, medications, and medical devices are created, tested, produced, marketed, and distributed to make sure they adhere to regulations for human consumption. Experts in regulatory affairs are in charge of making sure manufacturers follow all applicable laws and regulations at every stage of product development. Regulatory affairs are understood in a very specific way in the healthcare sector. Pharmaceuticals that are high-quality, safe, and effective are produced and distributed in accordance with its regulations. With the adoption of new rules and technological advancements, pharmaceutical formulation must now contend with new objectives and challenges.

Regulations, guidelines, and technologies

  • GMP
  • CGMP

Track 12: Modern drug delivery techniques

Recent years have seen the introduction of intelligent drug delivery systems that can immediately detect and react to pathophysiological situations, as well as a number of proteinic and other medications intended to target various cellular processes. Traditional small molecules and modern large molecules are typically administered without a precise molecular-targeting strategy or targeted at cell surface targets; these potential innovative medicines are different. To maximise their potential patient benefits, novel chemicals must be released in tissues and cells in a targeted and controlled manner, which calls for sophisticated drug delivery systems. The phrase "advanced drug delivery system" describes a method that boosts drug potency, controls drug release for a more protracted therapeutic effect, and raises safety levels before finally directing a drug to the right tissue.

  • New Technologies for Drug Delivery
  • Drug Delivery System for Implants
  • Child-friendly drug delivery methods
  • Routes for administering drugs

Track 13: New Advances in Drug Delivery Systems

Novel Drug Delivery Systems are techniques, formulations, technologies, and systems for safely delivering pharmaceutical drugs to their intended therapeutic effects within the body (NDDS). Drug delivery systems offer a lot of promise to enhance the therapeutic and diagnostic effects of medications because of their special characteristics. In contrast to other drug administration technologies, NDDS is a drug delivery mechanism. Innovative dosage forms that are vastly superior to conventional dosage forms are combined with cutting-edge technology. The Novel Drug Delivery System has a number of advantages, including the following: the ideal dosage at the ideal time and location, Excipients, production expenditures, and expensive drugs are all used more effectively. Patients gain from better therapies, higher standards, and greater quality of life.

  • Nanoencapsulation and nanodrugs
  • Controlled Drug Delivery System
  • Ocular Drug Delivery System
  • 2D & 3D Printing in Drug Delivery
  • Targeted Drug Delivery System
  • Controlled Drug Delivery System
  • Modulated Drug Delivery System
  • Drug Delivery: Devices and Equipment

Track 14: Pharmaceuticals and Drug Delivery Systems Using Nanotechnology

The potential for using nanoparticles as a drug delivery system is enormous. Nano systems with different compositions and biological characteristics have been extensively researched for use in drug delivery and gene delivery applications. Nanoscale materials are employed as diagnostic instruments or to deliver therapeutic medications to specific sites in a controlled manner in the field of nanomedicine and nano delivery systems, which is still relatively young but is swiftly expanding. Nano-drug delivery systems (NDDSs) are a class of nanomaterial that can prolong cycle duration, boost target cell or tissue absorption rate, reduce enzyme degradation, and improve drug stability and water solubility while also enhancing medication safety and effectiveness.

  • Nanoparticles: New Developments and Trends
  • Biomedical and Nanotechnology Applications
  • Systematic Drug Delivery Using Nanoparticulates
  • Non-Coding RNA Nanoparticle Delivery
  • Fabrication of Nanoparticles
  • How Big Data Can Aid Nanotechnology
  • Nanotechnology Clinical Translation
  • Nanoparticles for Screening and Immuno-Oncology

Track 15: Pharmacogenomics

Pharmacogenomics is an example of precision medicine, which aims to tailor medical treatment to each person or group of people. Pharmacogenomics is the study of how your DNA affects how you react to medications. Pharmacogenomics is the scientific study of how medications affect inherited genes. This includes how inherited genes affect how different people's bodies respond to different medications. Pharmacogenomics has many applications, including the correlation of individual genetic variation with pharmaceutical responses. Pharmacogenomics is one of the most significant components of personalised medicine.

  • Biology & Genetic Engineering
  • Genomic and Pharmacogenetic Research
  • Metabolism of drugs

Track 16: Pharmacology

Although commonly confused with pharmacy, pharmacology is a distinct field of study in the health sciences. Pharmacology is the study of how a medicine interacts with a biological system and the body. The study of medicines includes information on their chemical composition, biological effects, and therapeutic uses. These effects can be either therapeutic or harmful depending on a number of circumstances. Pharmacologists are frequently interested in two areas of study: toxicology, which examines the negative or toxic effects of medications and other chemical agents, and therapeutics, which focuses on how drugs and other chemical agents affect disease. Pharmacology includes a variety of disciplines, including those in medicine, pharmacy, nursing, dentistry, and veterinary medicine. Some of the most intriguing developments in modern medicine are being made at the cutting edge of pharmacology.

  • Neuropharmacology
  • Methods to modelling and computation
  • Pharmacology of regeneration
  • Individualized, exact medicine
  • Pharmacokinetics
  • Pharmacodynamics
  • Pharmaceutical Science of the Heart

Track 17: Preformulation Research

Preformulation is a set of studies that looks at the physicochemical properties of a potential drug candidate and how they might impact dosage form development and medication performance. This might be helpful for developing new products or proving the requirement of molecular modification. Preformulation research starts once the new chemical has been seeded. In a larger sense, it entails investigations into a molecule's physical, chemical, analytical, and medicinal properties as well as recommendations for altering the molecule to enhance its functionality. As a result, a preformulation research is a process for creating pharmaceutical formulations that applies and incorporates knowledge from the fields of toxicology, biochemistry, medicinal chemistry, and analytical chemistry.

  • Organoleptic and Bulk Characters
  • Examination of soluble compounds
  •  Analysis of stability

Track 18: Radiation-based medicines and biotherapy

The goal of biological or biologic therapy is to improve or restore the body's natural defence mechanism's capacity to fend against sickness and infection. A variety of malignancies and other disorders can be treated with biological therapy, sometimes referred to as biotherapy or immunotherapy. The use of biological response modifiers is common in biological therapy (BRMs). The body regularly produces these substances in trace levels as a defence against sickness and infection. With the use of contemporary laboratory methods, BRMs can be generated in vast quantities.

Biologically active substances known as radiopharmaceuticals are radionuclide-labeled to serve as a reliable source of ionising radiation for therapeutic and diagnostic reasons. Drugs called radiopharmaceuticals are used to identify and treat medical diseases. They may be given to the patient in a number of ways. For instance, they can be injected, injected intravenously, or placed in the bladder or eye.

  • Inhibitors of the tumour necrosis factor (TNF)
  • B-cell blockers
  • Inhibiters of interleukins (IL)
  •  Modulators of selective co-stimulation
  • Precursors for radiopharmaceuticals and their preparation
  • Radionuclide producer

Track 19: Research and development in pharmaceuticals

Research and development (R&D) is a crucial phase of drug development in the pharmaceutical (Pharma) sector. The research and development (R&D) of novel medications in the pharmaceutical sector. Some of the procedures include comprehending the illness and choosing a target—typically a cell's receptor site—that a therapeutic chemical can affect. R&D in the pharmaceutical industry is essential to policy because it justifies exorbitant costs and greater safeguards against normal price competition, which has historically been a source of innovation. The relationship between drug business costs, innovation rates, and prices has drawn public attention to pharmaceutical R&D.

  • Pharmacy, both commercial and physical
  • Chemical Biology in Pharmacology
  • Pharmacological Research Advances
  • Organic Pharmacy for Pharmaceuticals
  • Clinical Trials in Drug Delivery Systems and Clinical Research
  • RNA's new therapeutic pharmacological targets

Track 20: Safety of drugs and pharmacovigilance

No medication is completely safe, and all medications have the potential to cause negative effects. Pharmacovigilance is the process of identifying and responding to medication safety risks, and its use has grown over the past 10 to 15 years. Pharmacovigilance is a term used to describe the science and endeavours involved in the recognition, evaluation, comprehension, and avoidance of side effects or any other drug-related issue. Pharmacovigilance's main goal is to encourage the safe and efficient use of pharmaceuticals, particularly by providing timely information about their safety to patients, healthcare providers, and the general public. As a result, pharmacovigilance is an activity that supports patient safety and public health.

  • Adverse effects of drugs
  •  Investigations of cases and clinical data
  • High-Throughput Screening (HTS)

Track 21:Technologies for Formulation

Pharmaceutical formulation, in pharmaceutics, is the process of mixing several chemical components, including the active medication, to produce a finished pharmacological product. The terms dose form and formulation are commonly used in the same sentence. Although finding novel therapies is becoming more difficult, a drug's efficacy can be increased while reducing side effects by changing the way it is delivered. This procedure is referred to as formulation discovery. Modern or conventional formulation technologies can be employed in formulation discovery. Creating a stable and patient-acceptable medication formulation is the goal of formulation studies.

Creation and Development of New Modalities via Analysis

  • Preservative and Excipient Issues
  • New Excipients and Polysorbate Issues
  • New Lyophilization Developments and Alternative Drying Methods
  • Scalability, Robustness, and Developability

Track 22: The BBB for drug delivery

The brain is a very delicate and sensitive neuronal organ system that needs a constant supply of fuels, gases, and nutrients to maintain homeostasis and other important activities. Delivering drugs to the brain has been shown to be particularly difficult because of the blood-brain barrier (BBB). Only small molecules can pass through the BBB in a healthy brain, acting as a diffusion barrier to stop the majority of substances from entering the brain from the bloodstream. In the next 20 years, global drug development for brain diseases will need to significantly increase due to the rising numbers of seniors and patients with CNS issues. However, compared to other therapeutic areas, brain disease drug development has the lowest success rates.

  • Nanoparticle Delivery Throughout The BBB
  • Pharmacological Delivery to the Brain
  • In states of disease, the blood-brain barrier
  • BBB Models: New Approaches

Track 23 : Therapeutic Drug Transporters

Drug carriers are any materials used in the drug delivery process to increase the efficacy, safety, or selectivity of drug administration. Drug carriers are typically used to control a drug's absorption into the bloodstream. Systems created specifically for therapeutic drug delivery enable the precise and/or controlled release of pharmaceuticals. The treatment and potential cure of a variety of drug carrier systems are significantly impacted by many chronic diseases, including cancer. In the management of human diseases, nasal and pulmonary routes of drug administration are becoming more and more significant. These approaches present fascinating substitutes to parenteral medication administration, particularly for peptide and protein therapeutics. This can be accomplished by either releasing the medication slowly over time (often through diffusion) or by activating the release of the drug at the target site in response to an external stimulus, such as a pH change, the application of heat, or light activation.

  • Polymers in the Delivery of Drugs
  • Drug Delivery using Smart Materials
  • Transportation for drug
  • Drug Delivery Using Biomaterials





A product's potential reach and market penetration abilities can be verified by pharmaceutical market research studies. It is used by investors to value pharmaceutical businesses and the products in their pipelines. These businesses make use of it to keep an eye on the competition, spot future unmet requirements, and value their goods. With the help of PMRA, donors and grant makers can find pharmaceuticals that are being developed to treat particular diseases as well as their potential to find a cure for those diseases. Pharmaceutical companies must consider a product's potential, which is frequently based on the number of patients who have the indication that the drug is approved to treat. If other medications are currently authorised to treat that condition, a new medication must significantly outperform other medications to justify the expense of its research.

To avoid having to compete with the outcomes of already-approved medicines, many pharmaceutical companies will first test a product to treat a rare indication with none now available. Investors looking for stocks that give high returns on investment but having higher than average risk are very interested in the pharmaceutical industry. They utilise PMRA to calculate the potential profits a pharmaceutical business would see if the Food and Drug Administration (FDA) approves all of its upcoming drugs. Then, the revenue potential is compared to the market capitalization and stock price of the business. The items must first pass FDA inspection before earning doctors' trust in order for this income potential to materialise. In order to find the right items and businesses to support, grant providers and philanthropic non-profit organisations might use PMRA. Additionally, the PMRA can be used to assess treatment gaps and find goods with potential therapeutic benefits. The number of patients who can be treated with a treatment in development, the efficacy of the outcomes, and how soon the drug will be available on the market are all factors used by grant providers to make these decisions.

They can also decide if it can be tested on individuals who have the kind of indications they do. Pharmaceutical sciences market research and medication development Hong Kong, China's Bernard M. Y. Cheung University According to a recent Pharma industry research report by The Business Research Company, the worldwide pharmaceuticals market had a value of $934.8 billion in 2022 and would increase to $1170 billion in 2021, at a rate of 5.8%. Although this is a faster rate than the 5.2% for the years prior to 2017, it is slower than the growth rates of the other two major healthcare segments, medical equipment and healthcare services. Healthcare as a whole is expanding at a rate of over 7% each year. The launch of significant new drugs has slowed, and businesses are limiting their R&D investment, which helps to explain why the Pharma market is currently growing at a relatively moderate rate. For instance, Pfizer has discontinued its Alzheimer's research programme, while AstraZeneca and GSK have scaled back, despite the enormous promise for any novel, safe, and effective medicine to treat the condition. The development of a new medication costs an average of $2 billion, and big pharma companies' returns on investment are declining, going from 10.1% annually in 2010 to 3.2% annually in 2022. according to Deloitte's are preventing the introduction of expensive new breakthrough pharmaceuticals like those that bolstered the market in previous years. Instead, the growing global ageing population is fueling demand for long-term therapies for chronic diseases and improving access to healthcare in emerging economies, which are both driving development in the pharmaceutical business.

The size of the pharmaceutical market is influenced by a number of factors, including the prevalence of diseases, the cost of medications, consumer attitudes, governmental regulations, and certain supply-side factors:

•         Population size, age, genetics, and behaviour are all connected to illness prevalence (infectious disease incidence is lower where sanitation practises are better; sedentary lifestyles also encourage chronic disease).

•         Both medicine pricing and affordability are influenced by income.

•         Consumer attitudes range from a readiness to adopt complementary therapies to a mistrust of drug use.

•         Policies of the government (and insurance companies) have an impact on who pays for reimbursement. Regulation is determined by other laws, which might be a big obstacle for the introduction of new drugs.

•         Access to a suitable therapy, which may depend on quantity, as in an epidemic, is a key supply-side factor.

•         The growth of the healthcare market, where medications play a significant role, is being influenced by current and future changes in political, economic, social, technological, legal, and environmental issues. The growth of the healthcare industry is fueled by the following factors:

•         In the USA, taxes and drug costs have been decreased.

•         China and India's GDP growth rates of around 6%

In R&D, industrialised data services have made it possible to use clinical trial data in trial simulations. In the USA, regulatory hurdles for new treatments have been lowered. In high-population cities, pollution levels are high, which increases the prevalence of illnesses like asthma.

Health care spending per person is anticipated to increase from $1137 in 2017 to $1427 in 2021 as a result.

Restrictions and Drivers in the Pharmaceutical Market

The launch of significant new drugs has slowed, and businesses are limiting their expenditure in R&D, which is one explanation for the pharma market's current growth's relative sluggishness. For instance, Pfizer has discontinued its Alzheimer's research programme, while AstraZeneca and GSK have reduced their efforts despite the enormous potential for any novel, safe, and effective medicine to treat the condition. High failure rates, the $2 billion average cost of developing a new drug, and declining returns on investment (which, according to Deloitte's, fell from 10.1% a year in 2010 to 3.2% in 2017 for the big pharma companies) are delaying the introduction of pricey new breakthrough drugs like those that boosted the market in earlier years. Instead, the growing global ageing population is fueling demand for long-term therapies for chronic diseases and improving access to healthcare in emerging economies, which are both driving development in the pharmaceutical business.

Pharma Markets' Changing Geography

Although Asia Pacific has surpassed Western Europe as the second largest region, North America and Western Europe still make up 56% of the worldwide market due to growth over the past few decades. The introduction of low-cost generics has made medications more accessible, which has spurred growth in the Asia Pacific region. Other reasons that assist expansion in the Asia-Pacific region include the region's rising GDP per capita, government healthcare initiatives, and fast urbanisation, which puts pharmacies and doctors' offices within easy reach of expanding people. Up until 2021, Asia Pacific pharmaceutical sales will increase by 8.4% annually.

Important Pharmaceutical Market Segments

Musculoskeletal medications have the largest pharmaceutical market in the world. Treatments for conditions such rheumatoid and osteoarthritis, osteoporosis, carpal tunnel syndrome, tendonitis, rotator cuff tears, muscular dystrophy, myasthenia gravis, lupus erythematosus, and others are available. Major medications in this category include Felden, Dolonex, Piroxicam Pfizer, and Piroxicam Glaxo. In 2017, the market category made about 14% of the overall global market. The second, third, and fourth largest markets are for anti-infective, cardiovascular, and cancer medications.

The pharmaceutical market will experience the quickest growth until 2021 in the area of drugs for the treatment of diseases of the thyroid and pituitary glands as well as metabolic disorders like diabetes. Despite a recent rise of 11.6%, this market category will continue to develop at a rate of 9% per year in the future and will hold the fifth-largest market share.

With a market value of over $85 billion in 2017, anti-diabetic medications are the largest subsegment of the global pharmaceutical market. Anti-virals and anti-hypertensives are the next two most valuable segments. The fastest-growing subsegments include medications for some of the less common diseases, including thyroid, skin, and ovarian cancer. The US Federal Drug Administration has permitted a less stringent regulatory process and lower endpoint benchmark for cancer treatments, which is accelerating the rate of innovation.

Top Pharmaceutical Companies & the Competitive Environment

Pharmaceutical medications are governed by a plethora of laws and rules that address patenting, testing, safety, efficacy, and marketing. These laws and rules also have an impact on the market's size and growth rates. These can be entry-level impediments for small businesses, along with the substantial R&D expenses related to developing novel medicinal solutions. Pharmaceutical firms do, however, manufacture both branded and generic medications. For smaller players, generics, which are copies of medications whose patents have expired, present opportunity. They are gaining market share, especially in poorer nations where the government is promoting their manufacturing to increase access to less expensive medical care.

Top pharmaceutical companies on the market as a whole include:

•         Novartis

•         Sanofi

•         Pfizer

•         Hoffman-La Roche

•         Gilead

The top ten pharmaceutical companies collectively account for 30% of global sales, resulting in a moderately fragmented market. The share of these pharmaceutical businesses varies, nevertheless, depending on the segment: Hoffman-La Roche is, in a sense, the market leader for large-scale oncology medications, whereas Sanofi is the market leader for cardiovascular and metabolic illnesses.

The top players in markets where biologics have established a foothold are not among the top ten pharmaceutical manufacturers: For example, Bristol-Myers Squibb and Eli Lilley have large market shares in cancer, while Biogen is the market leader in the central nervous system sector.

Dealmaking in the healthcare sector has increased significantly in recent years. Increasing product portfolios and broadening the market reach of goods and services are the main goals of most mergers and acquisitions. For instance, in August 2021 Merck paid around $4 billion to acquire Idenix Pharmaceuticals Inc., a pharmaceutical business in the trial stage. Merck added the prospective hepatitis medications from Idenix through this acquisition, strengthening its product line.

According to The Business Research Company's most recent Pharmaceutical Drugs Market Global Report 2017, the robust growth of the Chinese pharmaceutical industry attracts foreign investors (TBRC).

Half the size of the pharmaceuticals market in the USA in 2016, the Chinese market was estimated to be worth $155 billion. The market is expected to increase at the quickest rate of all the nations included in the report, 10%, from 2016 to 2020, according to TBRC. A combination of an ageing population, busy lives, and an uptick in diabetes and cancer cases can be used to explain this rapid expansion.

Brazil and India both offer pharmaceutical businesses additional lucrative business opportunities. With growth rates of 9.6% and 7.8%, respectively, both nations are predicted to experience rapid expansion.

$27 billion was the estimated value of the Indian medicines market in 2016. By 2020, TBRC anticipates a 1.5-fold increase in the market. The country's changing lifestyles are to blame for such quick change. Due to the country's growing number of sedentary job profiles, India anticipates having roughly 100 million diabetic patients by the year 2030. The need for diabetes medicines will increase as a result.

By 2020, Brazil's medicines market is expected to surpass $60 billion. The healthcare sector in Brazil, which is going through a significant transformation and is experiencing new business dynamics, will be the market's main driver of growth. This makes the home market in Brazil one of the most promising and alluring in the whole world.

$27 billion was the estimated value of the Indian medicines market in 2016. By 2020, TBRC anticipates a 1.5-fold increase in the market. The country's changing lifestyles are to blame for such quick change. Due to the country's growing number of sedentary job profiles, India anticipates having roughly 100 million diabetic patients by the year 2030. The need for diabetes medicines will increase as a result.

By 2020, Brazil's medicines market is expected to surpass $60 billion. The healthcare sector in Brazil, which is going through a significant transformation and is experiencing new business dynamics, will be the market's main driver of growth. This makes the home market in Brazil one of the most promising and alluring in the whole world.

To maintain businesses in a highly competitive climate, TBRC advises pharmaceutical companies to boost the volume of merger acquisitions across the sector. This approach will enable businesses to create cutting-edge goods, services, and solutions while also exchanging knowledge and talents. For instance, Abbvie recently announced a partnership with Google-backed life sciences company Calico to establish a research and development centre for the discovery of pharmaceuticals and the creation of cures for people suffering from age-related disorders like cancer.

We would like to express our gratitude to all of our fantastic Keynote Speakers, Speakers, Conference Attendees, Students, Media Partners, Associations, Sponsors, and Exhibitors for helping to make the Pharmaceutics Conference a success!

The Conference Series LLC Ltd presented the 15th International Conference on Pharmaceutics and Drug Safety from June 15-16, 2022 in Amsterdam, Netherlands. The Organizing Committee Members, as well as scientists, researchers, students, and leaders from many sectors of biopharmaceutics, biotech, medical, and pharmacy, gave generous responses and active involvement, making this event a huge success. 

We really appreciate the contributions of all of our fantastic Speakers, Conference Attendees, Students, Media Partners, Associations, and Exhibitors who helped to make Pharmacovigilance 2022 Conference the finest one yet!

Exploring Latest Trends in Pharmacovigilance and Clinical Trials in the Age of COVID-19 was the theme of the 15th International Conference and Exhibition on Pharmacovigilance & Drug Safety, presented by Conference Series llc LTD, which took June 15-16, 2022 in Amsterdam, Netherlands.. The members of the organising committee, as well as scientists, researchers, students, and leaders from a variety of sectors related to pharmaceutics and drug delivery systems, generously responded and actively participated in the event, which was greatly enhanced by their efforts.

Conference Series thanks the conference moderator, Patricia, who is the coordinator of the pharmacovigilance programme.

The keynote forum's honourable attendance served as the conference's official start. The list includes:

Dr. Robert Weber, Oracle Health Sciences, Germany

Dr. Chaitanya N. Hiremath, founder, president, and chief executive officer of APODvision, Inc., Massachusetts, USA

Dr. Kai Heib, president and chief executive officer of INTLAB, Switzerland

Dr. Massoud Toussi, IQVIA, Paris, France

Dr. Lingli Zhang, West China Second University Hospital, Sichuan University, China

Karl-Dietrich Hatz, CMOO of INTLAB in Switzerland

Saudi Arabia's ALMAAREFA UNIVERSITY and Dr. TURKI ALOZAYB are both pharmacists.

Francesca Rollo, Italian firm Viatris

Additionally, there are more students and delegates...

Conference Series LLC Ltd expresses its profound gratitude to organisations such as Pharma Voice, Event listing sites, and other notable individuals that helped promote the conference through various online and offline channels, allowing it to reach every part of the globe. The meeting consisted of several sessions in which the following important scientific tracks were discussed:

The Conference Series Group extends its sincere gratitude to the following media partners: Conference, THE PHARMA WORLD, The British Society of Toxicological Pathology (BSTP), Crowd Reviews, Tabeeby,, Atlas of Science, and other illustrious individuals who assisted in organising the conference by moderating the discussion forums. The Keynote Speakers, Members of the Organizing Committee, Chairs, and Exhibitors who supported this event were also honoured by Conference Series.


  • 50% accommodation & Registration cost cover by conference sponsors.
  • 80% discount on the publication of the full length article in our supporting journals.
  • Editorial published free in Special Issue of journal: 1 Editorial/Issue
  • Digital and Conference Publicity through Photo and affiliation details in Banner
  • Can launch a book/chapter in the conference or be a poster judge
  • Awards will be given for the best research paper as well as best paper presentation.                

Join our team Drug Safety 2023 in this beautiful city London and let us make this professional gathering a Great success.



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Conference Date September 08-09, 2023
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