Recommended Global Pharmaceutical Sciences Webinars & Conferences
Drug Safety 2021
On the behalf of Drug safety department, I am glad to invite all the eminent scientists, academicians, young researchers, Business delegates and students from all over the world to attend the 14th International Conference on Pharmaceutics Drug Safety August 06-07,2021, London, UK.
This conference shares recent research and technologies, which gains tremendous interest with huge and exhilarated presence of skilled, young and intelligent researchers, business delegates and talented student communities.
Main goal of this conference is to bring together, professional group of scientists and researchers from all over the world to present and exchange advance ideas related to drug safety. It globalize the standard research in general, thus making discussions, presentations more internationally competitive and focusing attention on the recent outstanding achievements in the field of drug safety, and future trends and needs.
Since conference covers global aspects on drug safety, anyone interested in future progress of drug safety should not miss.
We’re eagerly anticipating to an excellent meeting with brilliant scientists from different countries around the world and sharing new and exciting results in drug safety which will be held on August 06-07, 2021, London, UK
This Pharmaceutics Drug Safety Conference focuses on the future of pharma and new technologies in drug safety.
Scientific Sessions of drug safety includes applications, Significance & Scope, Clinical Pharmacy and its Role in Treatment, Pre-Clinical and Clinical Trials, and Risk Management, Clinical drug toxicity and biomarkers, for medicines.
Main motive of this conference is to bring multidisciplinary community of scientist and young researchers from all over the world together to share views and new ideas regarding research technologies related to drug safety.
14th International Conference on Pharmaceutics and Drug Safety is the world's leading pharmaceutical conference. The two-day conference on pharmaceutical sciences will have more number of sessions and sub session on newfangled researches in the field of pharmaceutical sciences around the world. Drug Safety 2020 will involve 16 imperative sessions proposed to offer broad sessions that states issues in diverse fields of research and pharmaceutical sciences.
The participants can find complete sessions and panel discussions on latest discovery in drug safety and Pharmaceutical Sciences.
- Lectures from speakers
- Keynote forums by Prominent Professors, Doctors
- Open Innovation Challenges
- Poster presentations by Young Researchers
- Global Networking sessions with 50+ Countries
- Novel techniques to benefit your research
- Best platform for Global business and Networking opportunities
- Meet the editors of referred journals, Society and Association members across the Globe
- Excellent platform to showcase the latest products and formulations in Pharma C
Meet your subject matter expert (SME)
You all have excellent opportunity to meet brilliant scientist and businessman around the word, during session you can asked them questions, discuss your quarries, content, identify the objectives, and research related to drug safety. Subject matter experts will guide you in recent Research & developments.
The international pharmaceutics and drug safety software market is assured to grow at a compound annual growth rate of 6.5% during 2014-2019, expected to achieve a value of $154.1 Million in 2019. As of 2014, North America bears the highest share of international Pharmacovigilance and drug safety software market, followed by Europe. Although, Asian and Latin American countries shows highest growth market, rise in research outsourcing by pharmaceutical giants and growing public and private investments in pharmaceutical R&D in these emerging nations
- Services & Software’s
- Reporting & Monitoring
International pharmaceuticals market was structured at $934.8 billion in 2017 and will reach $1170 billion in 2021, growing at 5.8%, according to the report of current Pharma market research by The Business Research Company.
Speed up growth compared to 5.2% for the years before 2017 but slower than other two large healthcare segments, medical equipment, and healthcare services. Healthcare is growing at over 7% per year.
In the overall market, top pharmaceutical companies includes
- Hoffman-La Roche
Track 1: Pre-clinical and clinical trails
Clinical trials allow drug testing for safety assessment in different population. Preclinical development referred as preclinical studies or nonclinical Studies, is a research stage carried at initial level of increasing accessibility and iterative testing and drug safety data are collected. Main goals of preclinical studies to determine the safe dose in first phase and evaluate the product safety profile. Product may include drugs, gene safety, and diagnostic tools.
- Clinical trials on drugs used in respiratory disorders
- Regulatory authorities and ethics committee
- Multi center trials and monitoring
- Alternative trials design and models
- Data collection and quality control
- Bioassay and its types
- Designing of trials: pre-clinical studies
- Scientific Models for Pre-Clinical and Clinical Trials
- Pre-Clinical Testing
- Mechanism of adverse drug reactions
- Recent clinical trials on AIDS
- Classification of various adverse drug reactions
- Expected and un-expected drug reactions and its reporting
Track 2: Adverse drug reactions
Adverse drug reaction is a form of toxicity or increase drug effect which mainly occurs during efficient use. In US 3-7% hospitalization are due to ADRs. ADRs occur during 10-20% of hospitalizations, 10-20% of ADRs are severe. ADR’s showed no pharmacokinetic effects resulting in 0% death incidence till date. Suggested rate of 0.5 – 0.9% may be high because patient have some serious disorder. Severity and incidence vary through patients characteristic and through drug factors.
Track 3: Good Pharmacovigilance practice
Good Pharmacovigilance practice and pharmacoepidemiology in risk management to increase the possibility of beneficial effects of drug and adverse effects in population maintain reporting practice to avoiding the major problems in risk management. Also concentrate to examine information by collecting drug effects, caused by medicine. Pharmacovigilance and clinical trial services should have Pharmacovigilance certification.
Track 4: Pharmacy practices and its challenges
Pharmacy practice develops the professional role of pharmacists. Include disease state management, pharmacy professional development pharmaceutical drug, clinical drug intervention, pharmaceutical compounding, health physiology drug incompatibility and community pharmacy.
Track 5: Biopharmaceutical sciences
In this track we will discuss about rational drug management of cancer, diabetes, cardiovascular disorder and management of psychiatric disorders and autoimmune disease. Bioavailability and bioequivalence study plays an important role. International market for biopharmaceutics in 2013 was $ 305.1 million and expected to reach $ 326.3 million in 2014.
TRACK 6: Clinical trials on various disorders
- Emerging technology in clinical trials
- Recent clinical trials on AIDS
- Clinical trials on benign and malignant tumors
- Clinical trials on cardiovascular diseases
- Clinical trials on diabetes
- Clinical trials of monoclonal and polyclonal antibodies
- Clinical trials on drugs used in psychological disorders
- Applications of biomarkers in clinical trials
Tracks 7: Data quality management and analysis
Data quality management and analysis in drug safety depend on information collected from individuals. Quality management involves quality control, quality planning, quality assurance, and quality improvement. First step of data collecting cycle is collection of data in system, data entry. Second step is data storage, maintenance followed by data selection. In last data is analyzed. Finally process is concluded to analyze the data.
- Data Quality Control and Assurance
- Quality Planning and Improvement
- Data Safety Monitoring
Track 8: Significance and scope
Its significance Increase the impact of drug safety on patient welfare. This track gives the brief discussion about drug safety and pharmacy in healthcare system. Drug safety protection gives an outlook on the rules and laws to follow in drug safety and pharmacy practice. The Role of Pharma industries works in the improvement of drug safety system crucial to maintain analyze safety assessment data, its Detection and Evaluation of signals manual and medical devices reporting.
Clinical trial industry is repeatedly growing with diversified clinical research technologies and new clinical studies are being launched at an ever-growing pace. Clinical trials have always been a crucial part of the medicine development process, they provide clinical data for treating pathological disorders and diseases. The importance of diversity in industrial clinical trials and clinical research is to ensure that industrial clinical trials are doing diligence and being strategic possible in results. This diversity makes better understanding in the field of drug safety.
Track 10: Drug Safety
Statistics is playing an important role in clinical research in regulatory submission. Adverse drug reactions report can also be considered for the regulatory submission. Pharmacovigilance process is achieved by ICH guidelines.
Track 11: Case report in clinical
The study plays crucial role in clinical research program which can be an unexpected association between disease disorders or symptoms like unexpected event occurring during diagnosis, treatment, pathogenesis or adverse effects of diseases. Notable Variation in anatomical structure, therapeutic approaches or salient features is core objective focused in care report.
Track 12: Quality assurance
Track 13: Pharmacoepidemiology
In Pharmacoepidemiology we will examine the uses and effects of drugs on the population. This is the branch of pharmacology and epidemiology Thus, Pharmacoepidemiology is the bridge between pharmacology and epidemiology. In pharmacology we will read about the effect of drugs while in clinical pharmacology we will read about the effect of drugs on clinical humans. Clinical pharmacology provides a risk benefit assessment by effects of drugs in Patients body.
- Study about pharmacology
- Study about epidemiology
Track 14: Prevalence of Potential Drugs
The main purpose of this study is to evaluate the prevalence and explain the characteristics of PDDIs in medical recommendation of hospitalized surgical patients. In this transverse study, we examine 370 medical prescriptions from the surgery unit of a Mexican public teaching hospital. The classification and identification of potential drug-drug interactions were performed with the Micromedex 2.0 electronic drug information database. Results were examined with illustrative statistics and we estimated OR (odds ratio) to determine associated risk factors.
- Study of Medscape Drug Interaction Checker
Track 15: Recent trends in pharma and technology
Every industry is developed more rapidly. Products and administrations are growing increasingly at commercial level. Evolution plays an important part in inquire about and improvement, showcasing and promoting, and deals and dispersion. Only pharmaceutical division has speculated the investigation and advancement over the past few years and also in other sections in a decade time.
- Body sensors clinical trail
Track 16: Pharmaceutical sciences
The Pharmaceutical science is an extortionate scope of logical controls of revelation and advancement of newly developed medications and treatments. Pharmaceutical sciences includes the basic fundamental standards of physical and compound science, designing, organic chemistry, and science to see how to upgrade transference of medications to the body and make an interpretation of this coordinated comprehension into as good as ever treatments against human ailment.
Track 17: Drug regulation
Drug regulation is a process by which we can control the use of drug by international agreement and through some regulatory authorities like US Food and Drug Administration (FDA), the European Medicines Agency (EMA) and the Japanese Pharmaceutical and Medical Devices Agency (PMDA).
Track 18: Clinical Data Base Management
Clinical data management (CDM) is a complicated process in the field of clinical research, which posses to generation that are of high-quality, reliable, and statistically sound data from clinical trials. The main aim of CDM is to give the sureity about the final data collected from the research.
Track 19: Consulting and business opportunity
Due to some changing resources it is necessary to full-fill the regulatory requirements. Regulatory Affairs department is continuously developed and growing, and the one which is minutely affected during the Acquisition, Merger and recession. The international drug safety market and Business opportunity was valued at USD 2,408.0 million in 2013 and is predicted to increase at a CAGR of 12.6% at the time of forecast period. And on the second position it was Phase III clinical trial market and was valued at over USD 750.0 million in 2013.
- Drug safety software Development Companies
- Business Opportunities for drug safety Software Developing Companies
- Opportunities for drug safety Software Services companies
- Career Growth in drug safety Consulting
Past Conference Report
All accepted abstracts will be published in respective Conference Series LLC LTD International Journals.
Abstracts will be provided with Digital Object Identifier by