Regulatory Authority Compliance
With more stringent compliance parameters set by the USFDA the quality assurance of pharmaceutical products is ensured. In addition to cGMP, GLP and GCP practices as per the US Federal law pharma products should comply with 21CFR regulations. Also on a regular basis the FDA organizes compliance programs for the pharma industries in program areas like Biologics (CBER), Bioresearch Monitoring (BIMO), Devices/Radiological Health (CDRH), Drugs (CDER), Food and Cosmetics (CFSAN), Veterinary Medicine (CVM). The results of regulatory audits NAI – No Action Indication, VAI – Voluntary Actions Indicated, OAI – Official FDA Action Indicated are also critical to decid
- Food and Drug Administration (FDA)
- Medicines and Healthcare Products Regulatory Agency (MHRA
- Therapeutic Goods Administration (TGA)
- Central Drug Standard Control Organization (CDSCO)
- European Medicines Agency (EMEA)
Related Conference of Regulatory Authority Compliance
April 07-08, 2025
4th International Conference and Expo on Pharmaceutics & Novel Drug Delivery Systems
Vancouver, Canada
May 16-17, 2025
8th International Conference on Pharmaceutical Research
&
Innovations in Pharma Industry
Rome, Italy
June 02-03, 2025
31st International Conference on Advanced Clinical Research and Clinical Trials
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24th International Conference on Medicinal and Pharmaceutical Chemistry
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July 21-22, 2025
11th International Conference on Antimicrobials & Antibiotic Resistance
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August 25-26, 2025
11th International Conference on Pharmaceutical Regulatory Affairs and IPR
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42nd International Conference on Drug Discovery and Drug delivery system
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10th International Conference on Future Pharma and Innovations
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28th International Conference and Exhibition on Pharmaceutical Formulations
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November 27-28, 2025
4th World Conference on Pharma Industry and Medical Devices
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Regulatory Authority Compliance Conference Speakers
Recommended Sessions
- Pharmaceutical Research and Development
- Adverse Drug Reactions
- Causality Assessment
- Clinical Data Management
- Clinical Database Management
- Clinical Research and Statistics
- Clinical Research Nursing
- Clinical Trial Protocols
- Clinical Trials Pharmacovigilance
- Drug Delivery Technologies & Drug Designing and Development
- Drug repurposing to treat Viruses: COVID-19
- Drug Safety
- Drug Safety and Pharmacovigilance
- Global Clinical Trials
- Importance of Audit in Pharmaceutical Industry
- Medical Devices for Drug Delivery
- Pharma Market Research
- Pharmaceutical Nanotechnology: Challenges and Opportunities
- Pharmacoeconomics
- Pharmacokinetics and Pharmacodynamics in Drugs
- Pharmacovigilance and Clinical Trials
- Pharmacovigilance and Cosmetovigilance
- Pharmacovigilance and Risk Management
- Pharmacovigilance Practice
- Pharmacovigilance Significance and Scope
- Prevalence of Potential Drug- Drug Interaction
- Recent trends in Pharma and Technology
- Regulatory Authority Compliance
- Track: 29 Oncology Clinical Research
- Track:30 Risk assessment and management in clinical trials
- Use of Nanoparticles in DDS and Newer Methodologies
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- Smart Drug Delivery Systems - Pharmatech 2025 (Canada)
- Smart Drug Delivery Systems - Formulations 2025 (France)
- Smart Drug Delivery Systems - PHARMACEUTICA 2025 (Germany)
- Smart Polymers for Drug Delivery - Pharmaceutica-2025 (Canada)
- Solid Dosage Forms - Formulations 2025 (France)
- Stem Cell and Genetic Clinical Research - Clinical Research 2025 (Netherlands)
- Sustainability and Global Health Biotechnology - Biotech-2025 (France)
- Synthetic and Bioorganic Chemistry - PHARMACEUTICAL CHEMISTRY 2025 (Italy)
- Targeted Drug Delivery and Controlled Release Systems - PHARMA CONFERENCE-2025 (France)
- Targeted Therapies - Personalizedmedicine-2025 (Switzerland)
- Targeted Therapies in Cardiovascular Regeneration - Cardiovascular-2025 (France)
- Targeting the Renin-Angiotensin-Aldosterone System (RAAS) - Cardiovascular-2025 (France)
- 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)
- Toxicology - Pharmacology 2025 (France)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Types of Formulations - Formulations 2025 (France)
- USFDA Approved Biosimilars - Eurobiosimilars 2025 (France)
- Vaccine Delivery Systems - Pharmaceutica-2025 (Canada)
- 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)
- Wearable Drug Delivery Systems - PHARMA CONFERENCE-2025 (France)