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FDA Compliance Conferences

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GCP violations and Site Mistakes commonly found During a FDA Investigator Site Inspection/Audit and how to avoid them

This GCP training will guide you through key component identification of a good GCP audit program, Investigator awareness, Protocol adherence, The Informed Consent process, Evaluation of subject selection, Inclusion/exclusion criteria, data sampling and audit findings assessments.

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
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
Strategic Software Validation Planning for Executives and Managers - Webinar

This training webinar will discuss how to approach Strategic software Validation planning so as to satisfy FDA by complying to new enforcement initiative by FDA.

By : Compliance Online
Product Type : On Demand Webinar
Validation of Existing/ Legacy Computer Systems for FDA/EU Compliance

This webinar on validating legacy computer systems will give a good understanding of FDA and EU regulatory requirements for validation (retrospective validation) and provide tools for effective implementation.

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
Process Robustness: The New FDA Paradigm

Learn more about process robustness, the new FDA paradigm.

By : Compliance online

14 Jan, 2016 - 14 Jan, 2016
California / Palo Alto
Organizational Change Management Practices for FDA-Regulated Computer Systems

Organizational Change Management Practices for FDA-Regulated Computer Systems

By : ComplianceIQ

15 Dec, 2015 - 15 Dec, 2015
California / San Bruno