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FDA Compliance Conferences

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Controlling Change to meet GMP Requirements

This change control webinar will discuss the change control activities and documentation required to meet GMP requirements

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 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
Equipment Calibration, Maintenance, and Validation: What Auditors Look for in a Controlled Proce

This webinar will discuss the different aspects which auditors generally look in equipment calibration, maintenance and validation and highlight the best practices.

By : Compliance Online
Product Type : On Demand Webinar
The 6 Most Common Problems in FDA Software Validation & Verification

This FDA Software Validation and Verification training/webinar will review the validation planning process with particular emphasis on avoiding six common pitfalls.

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