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FDA Compliance Conferences

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Introduction to FDA Good Documentation Practices

This FDA Good Documentation Practices training will introduce and explain the concept of Good Documentation Practices, and provide real-world examples of how to, and how not to, use GDPs.

By : Compliance Online
Product Type : On Demand Webinar
Raw Materials Risk Management in GMP Facilities: Avoiding GMP non-Compliance Due to Raw Material Issues

This webinar covers FDA’s expectations from GMP facilities regarding raw material vendor selection,expectations from quality control and documentation processes, and training requirements, with case studies.

By : Compliance Online
Product Type : On Demand Webinar
Responding to FDA Form 483s and Warning Letters

This training on responding to FDA Form 483s and Warning Letters will present methods for reviewing, evaluating, and writing responses to FDA Form 483s and Warning Letters.

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
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

> 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