Pharmaceutical cGMP, Data Integrity and FDA Inspections Current Challenges and Preparations 2016 is a conference that covers topics such as:
- CGMP for APIsBuildings & Facilities, Equipment, Control of Components
- CGMP for Finished Pharmaceuticals
- Documentation, Change Control, Process Validation
- Production and Process Controls, Laboratory Controls
- Data Integrity
- Quality Protocols
- FDA Inspection Guides
- Electronic Records and Signatures
- Recent FDA Warning Letters
- Top 10 most common cited FDA Inspectional Observations (cGMP deficiencies)
- Indian Pharma and Challenges Ahead
Pharmaceutical cGMP, Data Integrity and FDA Inspections Current Challenges and Preparations 2016 brings together attendees involved or interested in:
- Quality Control & Quality Assurance
- A must attend seminar for professionals in Pharmaceutical development and quality control companies, Manufacturers of drug substances (APIs), Finished Products, Contract laboratories and Clinical Research Organizations
- Regulatory Compliance
- Research and Development Engineering
- Validation Production
- Manufacturing and Facilities
- Documentation Supply Chain and Logistics
