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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
FDA's Medical Device Software Regulation Strategy: 2-Day Virtual Seminar by Ex-FDA Official
Virtual Seminar | Feb 9-10, 2021
Coping with FDA Import Delays, including COVID-19, Expedited Imports and Detentions: 2-Day Virtual Seminar
Virtual Seminar | Feb 23-24, 2021
Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries): 2-Day Virtual Seminar by Ex-FDA Director
Virtual Seminar | March 29-30, 2021

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