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FDA Announces Flexible Manufacturing Approach for Cell and Gene Therapies on January 11, 2026

2 weeks ago talkbio0Tagged calcium glucarate, Candidiasis, Chronic Mucocutaneous, Cells, gene therapy, Manufacturing, Pliability, requirements, United States Food and Drug Administration

FDA; cell and gene therapies; CGT; manufacturing flexibility; CMC requirements; Marty Makary

Optimizing Pharmaceutical Supply Chains: The Evolving Role of Third-Party Logistics Providers

2 years ago talkbio0Tagged Administration occupational activities, Cold Chain Management, Pharma, Pharmaceutical Supply Chain, Regulatory Compliance, requirements, third-party logistics

Third-Party Logistics (3PL) Providers, Pharmaceutical Supply Chain, Pharma 4.0, Regulatory Compliance, Cold Chain Management, Data Mining and Management, Licensing Requirements