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Health & Medical Conferences

> Upcomings Conferences

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>Conference documentation and webinars for this Sector

Design History Files, Device Master Records, Device History Records, and Technical Files

This webinar will discuss in detail the existing and proposed requirements for the FDA's DHFs, DMRs, DHRs and the MDD's TF/DD.

By : Compliance Online
Product Type : On Demand Webinar
How to withstand an FDA audit of your facilities: A primer for clinical sites, manufacturing facilities

This webinar training will discuss the types of audit and what are the activities to be done before, during and after FDA audit to pass it successfully and how to increase credibility for your company.

By : Compliance Online
Product Type : On Demand Webinar
Integrating Clinical Evaluation and Risk Management (ISO 14971)

This clinical evaluation & ISO 14971 training will discuss how the new changes in MDD and the risk management requirements per 14971 overlap and how manufacturers can establish one integrated system to meet both the requirements.

By : Compliance Online
Product Type : On Demand Webinar
Dietary Supplements: Regulatory Compliance Requirements, Product Claims, Labeling Issues and FDA

This 90 minute interactive webinar will review the dietary supplement regulations and discuss how to verify that your products are compliant, while citing differences with food and drug regulations.

By : Compliance Online
Product Type : On Demand Webinar
Using an IQ / OQ / PQ Approach to Validating Medical Device Software

This Medical Device Software Validation training will show how you can validate software, using IQ / OQ / PQ methodologies typically employed for process validation.

By : Compliance Online
Product Type : On Demand Webinar