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Devices Compliance Conferences

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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
Clinical Evaluation Reports (CER's) Required for All Classes of Medical Devices in Europe

Understand what is the CER and how to prepare for and defend it and properly constructing a "bullet-proof Technical File and manage your documentation.

By : Compliance Online
Product Type : On Demand Webinar
Verification and Validation (V&V) of Software in the Medical Devices

This 90-minute presentation will cover the FDA Quality System Requirements for software used in medical devices. The presenter will review FDA guidelines on software verification and validation and discuss methods to verify and validate even complex software.

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

> Previous Conferences, Webinars and Training All Past Conferences >

Predictive Analytics World San Francisco 2016

Predictive Analytics World for Business is the leading event for predictive analytics professionals and managers. Register by Dec 18, 2015 and save $600. Take $150 off Early Bird or Two Day Pass fee by using discount code: CFS150 when registering.

By : Predictive Analytics World

3 Apr, 2016 - 6 Apr, 2016
California / San Francisco
Creating a value added Internal Audit Program

This webinar will cover creating of a value-added internal auditing program for compliance to FDA and ISO 13485 internal auditing requirements. It will include how to setup and manage the auditing system, as well as how to conduct an internal audit,and document the results and any non conformities.

By : Redstone Consultants

10 Dec, 2015 - 10 Dec, 2015
New York / New York
Process Validation - Overview of Why and How

Gain an understanding of FDA and ISO requirements for process validation and learn how to implement them.

By : Compliance online

18 Nov, 2015 - 18 Nov, 2015
California / Palo Alto