The 9th International Conference on Pharmaceutical Regulatory Affairs and IPR is dedicated to meeting standards of drug regulations & achieving GxP compliance.
Topics
- Current Regulations and Quality Standards
- Good Manufacturing Practices: The Gap within
- The Role of c in cGMP
- Current GMP Guidelines (cGMP) & GxP in Pharmaceuticals
- Quality Control
- Good Clinical Practices & Good Laboratory Practices
- Validation
- Quality Assurance
- Storage, Distribution, Transportation
- Contract & Sterile/Aseptic Manufacturing
- GMP in Food Industry
- Formulation Development
- Softwares in GMP and GCP
- GMP in Microbiology and Biotechnology
- Excipient Qualification and Supply Chain Controls
- Clinical Affairs and Regulatory Strategies Implementation
- Impact of Brexit on Regulatory Framework
- Penalties for Regulatory Non-compliance
- Regulatory Challenges for Medical Devices
- Regulatory Communications and Submissions
Who should Attend
Attendees involved or interested in:
- Manufacturing
- Quality Control
- Research and Development
- Scientists, practitioners, professionals
- Clinical Affairs
From:
- pharmaceutical industries, Biologics, Biosimilars, Food Technology Industries, Medical Devices
- Pharmacy Practice
- Quality Assurance
- Pharmaceutical sciences
- Clinical Practice
- Regulatory Affairs from Universities of Medicine, Pharmacy
