Regulatory Affairs
Administrative issues is a relatively new calling which created from the yearning of governments to ensure general wellbeing by controlling the security and viability of items in ranges including pharmaceuticals,veterinary drugs, therapeutic gadgets, pesticides, agrochemicals, beautifying agents and correlative meds. Regulatory Affairs is included in the improvement of new restorative items from at an early stage, by coordinating administrative standards and by get ready and presenting the pertinent administrative dossiers to wellbeing powers.
Regulatory Affair effectively required in each phase of improvement of another prescription and in the post-advertising exercises with approved therapeutic items. The Regulatory Affairs office is a vital part of the hierarchical structure of pharmaceutical industry. Inside it liaises at the interphase of medication advancement, assembling, promoting and clinical research. Remotely it is the key interface between the organization and the Regulatory powers.
- Career development in regulatory affairs
- Regulatory strategies and developments
- Regulatory communications and submissions
- Regulatory challenges for medical devices
- Regulatory requirements for pharmaceuticals
- Biologics and Biosimilars
Related Conference of Regulatory Affairs
September 22-23, 2025
20th International Conference on Pharmaceutical Formulations & Drug Delivery
Toronto, Canada
September 23-24, 2025
10th International Conference on Future Pharma and Innovations
Amsterdam, Netherlands
November 11-12, 2025
6th Annual Congress on Antibiotics and Bacterial Infections
Amsterdam, Netherlands
November 13-14, 2025
28th International Conference and Exhibition on Pharmaceutical Formulations
Paris, France
November 13-14, 2025
21st International Conference on Pharmaceutical Chemistry
Aix-en-Provence, France
November 25-26, 2025
4th World Congress on Medicinal Chemistry and Computer Aided Drug Design
Paris, France
November 27-28, 2025
4th World Conference on Pharma Industry and Medical Devices
Zurich, Switzerland
December 15-16, 2025
3rd International Conference on Current Advances In Pharmaceutical Industry And development
Amsterdam, Netherlands
January 28-29, 2026
23rd International Pharmaceutical Sciences & Life Saving Drugs
Bangkok, Thailand
June 08-09, 2026
25th International Conference on Medicinal and Pharmaceutical Chemistry
San Diego, USA
June 08-09, 2026
8th International Conference and Exhibition on Pharmaceutical Development and Technology
San Diego, USA
July 27-28, 2026
26th World Congress on Pharmaceutical Sciences and Innovations in Pharma Industry
Rome, Italy
July 27-28, 2026
19th International Conference and Exhibition on Pharmacovigilance & Drug Safety
Rome, Italy
August 20-21, 2026
32nd International Conference on Advanced Clinical Research and Clinical Trials
London, UK
November 19-20, 2026
14th International Conference and Exhibition on Natural Products and Medicinal Plants Research
Dubai, UAE
Regulatory Affairs Conference Speakers
Recommended Sessions
- Advances and applications in HPLC Techniques
- Analytical Chemistry
- Aqueous and Non-Aqueous Titrimetric Method
- Assay Methods Based on Separation Techniques
- Bioavailability and Bioequivalence
- Degradation and Impurity Analysis of Different Dosage Forms
- Design and Analysis in Chemical Research
- Drug Formulation & Drug Design Pre-Formulation
- Errors in Pharmaceutical Analysis
- Industrial Pharmacy and Pharmacy Practices
- Innovations in Pharma Engineering
- Methods of Chromatography
- Modern Pharmaceutical Analysis
- Pharmaceutical Development and Technology
- Pharmaceutical Methods and Innovations
- Pharmaceutical Nanotechnology
- Quality Control, Quality Assurance and Regulatory Filings
- Regulatory Affairs
- Separation Processes in Chemical Manufacturing Industries.
- Spectroscopy in Pharmaceutical Analysis
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- Real-Time Safety Data Monitoring Strategies - Clinical Trials-2026 (UK)
- Real-World Evidence in Clinical Trials - Pharma Europe 2026 (UK)
- Real-World Evidence in Clinical Trials - Clinical Research 2026 (UK)
- Recent Advances in Pharmacology and Toxicology - Pharmacology 2026 (Italy)
- Regenerative Therapies and Stem Cells - Pain Management 2026 (France)
- Regulatory Affairs & Global Approval - Biologics Meet 2026 (UK)
- Regulatory Affairs and Drug Safety - PHARMACEUTICAL CHEMISTRY 2025 (France)
- Regulatory Affairs and Intellectual Property Rights - Future Pharma 2025 (Netherlands)
- Regulatory Authority Compliance - MedTech-2025 (Switzerland)
- Regulatory Harmonization & Compliance - Biologics Meet 2026 (UK)
- Regulatory Requirements for Pharmaceuticals - PHARMACEUTICAL SCIENCES 2026 (Italy)
- Regulatory Science and Clinical Trial Innovations - Euro Antibiotics 2025 (Netherlands)
- Regulatory updates on Biosimilars - Eurobiosimilars 2026 (Italy)
- Rehabilitation and Physical Therapy in Pain - Pain Management 2026 (France)
- Risk-Based Monitoring and Trial Optimization - Clinical Trials-2026 (UK)
- Safety Pharmacology - Pharmacology 2026 (Italy)
- Safety Reporting in Early Phase Trials - Clinical Trials-2026 (UK)
- Semi-Solid Dosage Forms - Formulations 2025 (France)
- Sexually Transmitted Bacterial Infections and Resistance Trends - Euro Antibiotics 2025 (Netherlands)
- Signal Prioritization and Management Techniques - Clinical Trials-2026 (UK)
- Single-Use Technologies in Production - Biologics Meet 2026 (UK)
- Site Management Innovation - Clinical Research 2026 (UK)
- Smart Drug Delivery Systems - Formulations 2025 (France)
- Solid Dosage Forms - Formulations 2025 (France)
- Stem Cell and Genetic Clinical Research - Clinical Research 2026 (UK)
- Stewardship Programs in Human and Animal Health - Euro Antibiotics 2025 (Netherlands)
- Structure-Based Drug Design and Molecular Docking - Euro MedChem and CADD 2025 (France)
- Supply Chain Management - Pharmaceuticals-2025 (France)
- Sustainable Antibiotic Practices and Global Policy - Euro Antibiotics 2025 (Netherlands)
- Sustainable Biologics Manufacturing - Biologics Meet 2026 (UK)
- Synthetic and Bioorganic Chemistry - PHARMACEUTICAL CHEMISTRY 2025 (France)
- Synthetic and Green Medicinal Chemistry - Euro MedChem and CADD 2025 (France)
- Systems Pharmacology and Drug Modeling - Euro Pharmacology 2025 (France)
- Target Identification and Validation - Euro MedChem and CADD 2025 (France)
- Targeted Drug Delivery and Nanomedicine in Infectious Diseases - Euro Antibiotics 2025 (Netherlands)
- Targeted Therapies - Personalizedmedicine-2025 (Switzerland)
- Technology in Pharma Sciences - MedTech-2025 (Switzerland)
- Telemedicine - Personalizedmedicine-2025 (Switzerland)
- The Future of Pharma R&D - Future Pharma 2025 (Netherlands)
- The Role of CROs in Clinical Trial Execution - Clinical Trials-2026 (UK)
- Toxicological Impacts of Air and Water Pollution - Euro Pharmacology 2025 (France)
- Toxicology - Pharmacology 2026 (Italy)
- Toxicology: Mechanisms and Risk Assessment - Euro Pharmacology 2025 (France)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Trending: Digital Health and Telemedicine for Rare Care - ORPHAN DRUGS 2025 (France)
- Types of Formulations - Formulations 2025 (France)
- USFDA Approved Biosimilars - Eurobiosimilars 2026 (Italy)
- Vaccine Development Against Bacterial Pathogens - Euro Antibiotics 2025 (Netherlands)
- Vaccines & Immunotherapy - Pharma Expo-2026 (Thailand)
- Women in Rare Disease Leadership and Science - ORPHAN DRUGS 2025 (France)