Pharma Manufacturing and Compliance
Drug manufacturing is the process of industrial-scale synthesis of pharmaceutical drugs by pharmaceutical companies. The process of drug manufacturing can be broken down into a series of unit operations, such as milling, granulation, coating, tablet pressing, and others.
Good manufacturing practice guidelines provide guidance for manufacturing, testing, and quality assurance in order to ensure that a manufactured product is safe for human consumption or use. Many countries have legislated that manufacturers follow GMP procedures and create their own GMP guidelines that correspond with their legislation. All guideline follows a few basic principles.
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Pharma Manufacturing and Compliance Conference Speakers
Recommended Sessions
- Adverse Drug Reactions
- Biopharmaceutical Sciences
- Clinical Trials and Research
- Clinical Trials on Various Disorders
- Data Quality Management & Analysis
- Data Quality Management and Analysis
- Drug Formulation & Analytical Techniques
- Drug Regulations
- Drug Safety
- Drug Safety and Pharmacovigilance
- Pharma Manufacturing and Compliance
- Pharmaceutical Care
- Pharmaceutical Sciences
- Pharmaceutical Technology
- Pharmacoepidemiology
- Pharmacovigilance and Risk Management
- Prevalence of Potential Drug- Drug Interaction
- Quality Assurance
- Recent trends in Pharma and Technology
- Regulatory Affairs and Intellectual Property Rights
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