Sterile Manufacturing Training

RFQ/OBP220/2025/26

Designing and delivering a comprehensive sterile manufacturing training program. Covering key regulatory requirements (e.g., EU GMP Annex 1, FDA 21 CFR Part 210/211, ISO 9001). Customizing content to suit (Viral Vaccines Manufacturing) product types (e.g., sterile injectables, biologics). Illustrations of Best Industry practice. Providing training materials, case studies, and assessments. Delivering training onsite, online, or hybrid, as mutually agreed. Offering certification of completion and a summary training report.

Request for Quote

2025/11/04 15:00:00

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RFQ/OBP220/2025/26