FDA Regulations for Food, Drugs, Biologics, Cosmetics, and Medical Devices Including IVDs 2014 is a webinar that covers topics such as:
- Definitions
- FDA Laws and Regulations
- Regulatory Requirements Subject to Manufacturers for Food, Drugs, Biologics, Cosmetics, and Medical Devices including IVDs
- Label and Labeling
- Regulatory Requirements for Investigational New Drug Application (IND)
- Good Manufacturing Practices for Food, Drugs, Biologics, and Devices including IVDs
- Common Non-compliance Issues and Consequences
- Regulatory Requirements for Investigational Device Exemption (IDE)
- Best Practices to Achieve Compliance and to Stay Compliant
- FDA Enforcement Actions: Recent Cases
- PASS-IT Suggestions and Recommendations
FDA Regulations for Food, Drugs, Biologics, Cosmetics, and Medical Devices Including IVDs 2014 is intended for:
- Pharmaceutical Compliance Professionals
- Medical Device Quality and Compliance Professionals
- Regulatory Affairs
- Quality
- VPs
- CEOs
- Clinical Affairs
- Attorneys
- Consultants
- R&D
- Anyone Interested in the Regulations Governing Food, Drugs, Cosmetics, and Medical Devices And IVDs
- Contractors/Subcontractors