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Compliance Training, Seminars by Ex-FDA Officials
Key Areas:
FDA Audits and Inspections | eCTD Submissions | FDA's GMPa Expectations | Regenerative Medicine | FDA Legal Authority | Promotion and Advertising | Stem Cell Treatments | Tissue Engineering | Gene Therapies | Off Label Use | Custom Device Promotion | Systematic Operating Procedures (SOPs) | Outsourcing Activities | First-in-Man Clinical Trials | IND Submission | Vendor Selection | Process Validation | Warning Letter | Foreign Inspections | FDA's New Import Program | FDA Recalls | CAPA
Managing GMP Compliance and Phase Appropriate GMP Considerations for Virtual Companies: 2-Day Virtual Seminar by Ex-FDA Director
Virtual Seminar | May 3-4, 2021
FDA Recalls - Before You Start, and After You Finish: 2-Day Virtual Seminar
Virtual Seminar | May 6-7, 2021
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