Current Regulatory Requirements for Aseptically Produced Products 2019 is an event dedicated to the manufacture of sterile products, whether by aseptic means or terminal sterilization.
Current Regulatory Requirements for Aseptically Produced Products 2019 covers topics such as:
- Current regulatory requirements and guidance documents dealing with sterile products
- Six quality systems that are reviewed during regulatory inspections
- Expectations for aseptically produced products.
- The importance of personnel training and control of microbiological contamination
- Common deficiencies cited with the manufacture of sterile drugs
Current Regulatory Requirements for Aseptically Produced Products 2019 intended for:
- Drug Manufacturers
- Sterile Product Vendors
- Contract Manufacturing Companies
- Quality Control Departments
- Quality Assurance Departments
- Validation Departments
- Manufacturing Departments
- Regulatory Departments
- Production Departments
