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Health & Medical Conferences

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>Conference documentation and webinars for this Sector

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
Pharmaceutical Water System Use & Monitoring

This webinar on pharmaceutical water systems will explain practical best practices for outlet use and sampling to reflect the true water quality and how to most effectively use the resulting data to improve manufacturing’s water use practices.

By : Compliance Online
Product Type : On Demand Webinar
The 510(k) Submission: Requirements, Contents, and Options - WEBINAR

This 510(k) training will discuss the submission process and the contents required by the FDA for a successful 510(k) submission. It will also provide an understanding of the common pitfalls, delays, and possible preventive measures.

By : Compliance Online
Product Type : On Demand Webinar
Delivering the national dementia strategy

The impact on the provision and delivery of dementia services, challenges, opportunities and the future of dementia care.

By : Laing & Buisson
Product Type : Academic Conferences
FDA Warning Letter Closeout Program - Webinar

This FDA warning letter closeout program will discuss how to successfully complete warning letter close out program which will help firm to obtain a closeout letter from FDA.

By : Compliance Online
Product Type : On Demand Webinar