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Health & Medical Conferences

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>Conference documentation and webinars for this Sector

How do I Keep FDA Happy with my Contract Manufacturer

This webinar will cover techniques and process that can help you assure reliability and consistent quality from your suppliers or contract manufacturers. You will learn how to monitor your supplier and ensure they meet FDA's quality requirements.

By : Compliance Online
Product Type : On Demand Webinar
Application of CAPA in (Device) Sterilization – For the Non-Expert WEBINAR

This webinar will review the typical non-conformances experienced in the (Medical Device) sterilization process and the course of action that should be taken by the manufacturer or contract sterilizer.

By : Compliance Online
Product Type : On Demand Webinar
Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs

This Medical device training will be discussing the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing products.

By : Compliance Online
Product Type : On Demand Webinar
Developing an ethylene oxide (EO) sterilization process for a product with limitations

This EO sterilization training Webinar will discuss how to modify EO sterilization process for complicated medical products which are sensitive to moisture, temperature, vacuum changes.

By : Compliance Online
Product Type : On Demand Webinar
Trial Master File for Research Sites: Can You Pass FDA Inspection?

This webinar on Trial Master File (TMF) for clinical research sites will show how you can create an FDA compliant TMF to ensure that it will pass inspection by FDA investigators and QA Auditors.

By : Compliance Online
Product Type : On Demand Webinar