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4th Technology Transfer for Biologics
A biopharma company’s very survival depends on its ability to maintain product quality throughout every step of clinical and commercial manufacturing. You must always be...
18 Oct 7:00 AM -
3 Hour Webinar: How the FDA is Trained on Medical Device Inspections
FDA Field Inspectors conduct administrative and enforcement activities related to the Quality System (QS) Regulation (21 CFR 820), the Medical Device Reporting (MDR) Regulation...
18 Oct 1:00 PM