Good Manufacturing Practices (GMP):
Good Manufacturing Practice is the part of quality management which ensures that products are consistently produced and controlled according to the quality standards appropriate to their intended use and as required by the marketing authorization, clinical trial authorization or product specification. Good Manufacturing practices conference aims at both production and Quality Control. Current Good Manufacturing Practices (cGMP) is aimed primarily at managing and minimizing the risks inherent in pharmaceutical manufacture to ensure the quality, safety and efficacy of products. FDA regulates the quality of pharmaceuticals very carefully. Current Trends in the FDA is the main regulatory standard for ensuring pharmaceutical quality.
- Facts about current good manufacturing practices (cGMPs)
- Good automated manufacturing practice (GAMP)
- FDA good manufacturing practices
- GMP/GCP interface & GMP audits
- GMPs for OTC and cosmetic products – global requirements
- GMPs for medical devices
- GMP requirements & standards
Related Conference of Good Manufacturing Practices (GMP):
May 16-17, 2025
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&
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Good Manufacturing Practices (GMP): Conference Speakers
Recommended Sessions
- Active Pharmaceutical Ingredients:
- Analytical strategies for pharmaceutical products:
- Biologics and Biosimilars :
- Clinical trials and Pharmacovigilance:
- Drug Delivery Technologies & Drug Designing and Development:
- Drug discovery and NCEs:
- Formulations and NNDS:
- Good Manufacturing Practices (GMP):
- Importance of Audit in Pharmaceutical Industry:
- Pharma Market Research:
- Pharmaceutical Auditing for OTC Drugs:
- Pharmaceutical Industry:
- Pharmaceutical Manufacturing, Scale Up and Tech transfer:
- Pharmaceutical Nanotechnology: Challenges and Opportunities:
- Pharmaceutical Packaging and Logistics:
- Pharmaceutical Research and Development:
- Pharmacoeconomics:
- QC & QA: Quality control and Quality assurance:
- Quality by design(QbD) approach:
- Regulatory Affairs:
- Regulatory Authority Compliance:
- Use of Nanoparticles in DDS and Newer Methodologies:
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- Technology in Pharma Sciences - MedTech-2025 (Switzerland)
- Telemedicine - Personalizedmedicine-2025 (Switzerland)
- The Future of Pharma R&D - Future Pharma 2025 (Netherlands)
- The Next Generation Approach of Antibiotics - Antibiotics Resistance 2025 (Canada)
- Toxicological Impacts of Air and Water Pollution - Euro Pharmacology 2025 (France)
- Toxicology - Pharmacology 2025 (France)
- Toxicology and Safety Pharmacology - Pharmacology-2025 (Spain)
- Toxicology: Mechanisms and Risk Assessment - Euro Pharmacology 2025 (France)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Types of Formulations - Formulations 2025 (France)
- Vaccine Design and Drug Design - PHARMA CONFERENCE-2025 (France)
- Vaccine Drug Delivery Systems - PHARMACEUTICA 2025 (Germany)
- Vascular Pharmacology: Focus on Endothelial Dysfunction - Cardiovascular-2025 (France)
- Veterinary Pharmacology - Pharmacology-2025 (Spain)
- Wearable Drug Delivery Systems - PHARMA CONFERENCE-2025 (France)