Pharmaceutical Regulatory Affairs and IPR of Biopharmaceuticals
Good Manufacturing Practices quality of drugs is essentially the responsibility of manufacturers. GMP Guidelines are means to assure this very quality of drugs. CGMP refers to the Current Good Manufacturing Practice regulations enforced by the US Food and Drug Administration (FDA). CGMPs provide for systems that assure proper design, monitoring, and control of manufacturing processes and facilities. Adherence to the CGMP regulations assures the identity, strength, quality, and purity of drug products by requiring that manufacturers of medications adequately control manufacturing operations. GMP is actually good common sense quality management quality assurance GMP production and quality control.
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Pharmaceutical Regulatory Affairs and IPR of Biopharmaceuticals Conference Speakers
Recommended Sessions
- Pharmaceutical Sciences: Academic and Industry overview
- Bioavailability & Bioequivalence studies of Biopharmaceuticals
- Biologics & Biosimilars
- Biopharmaceutical Companies & Market analysis
- Biopharmaceutical Drug Design and Development
- Biopharmaceutical Engineering
- Biopharmaceutical Pharmacovigilance
- Biopharmaceutical Regulatory Affairs and Intellectual Property Rights
- Biopharmaceuticals
- Biotechnology in Health care
- Clinical Trials and Research
- Clinical Trials on Biopharmaceuticals Products
- Drug Targeting and Design
- Genetics and Genetic Engineering
- Growth strategies of pharmaceutical industries
- Hospital & Industrial Pharmacy
- Nanoparticles-An Innovative Drug Delivery System
- Novel Drug Delivery Systems
- Pharmaceutical Analysis
- Pharmaceutical Care and Health Systems
- Pharmaceutical Formulations and Engineering
- Pharmaceutical Packaging and Marketing
- Pharmaceutical Regulatory Affairs and IPR of Biopharmaceuticals
- Pharmaceutical Research and Development
- Pharmaceutics and Pharmacotherapeutics
- Pharmacodynamics and pharmacokinetics
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