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Transfer of Analytical Procedures According to the New USP Chapter (1224)- Webinar

This webinar on transfer of analytical procedures will discuss USP and FDA requirements for method transfer between laboratories and sites, and provide tools for effective implementation.

By : Compliance Online
Product Type : On Demand Webinar
Laboratory Investigation Out-of-Specification Results - Webinar

In this Laboratory Investigation training learn what constitutes an OOS observation, what are the guidance’s process & Steps to be taken in the laboratory in the event of an OOS observation.

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
FDA's New Enforcement of 21 CFR Part 11 WEBINAR

Learn FDA requirements for 21 CFR Part 11, understand how to implement with the help of SOPs and case studies.

By : Compliance Online
Product Type : On Demand Webinar
Basics of testing associated with sterilization validation and routine processing

This sterilization validation process training webinar will review the FDA or ISO requirements for tests following validation and emphasis is placed on the appropriate tests for validation, the appropriate routine tests and the frequency of testing.

By : Compliance Online
Product Type : On Demand Webinar

> Previous Conferences, Webinars and Training All Past Conferences >

Pharma Summit 2016 – Risk Control & Compliance

The ComplianceOnline Pharma Summit 2016 - Risk control & Compliance aims to bring together FDA, Experts, Leaders and Veterans to discuss the most important challenges of Biotech, Pharma industry.

By : Compliance online

16 Jun, 2016 - 17 Jun, 2016
Pennsylvania / Philadelphia
Design of Experiments for Process and Product optimization

Attendees will learn to practice applying DOE techniques with various data sets. It will provide key tools and knowledge to be able to apply the methods effectively in their process and product development efforts.

By : Compliance online

16 Jun, 2016 - 17 Jun, 2016
Pennsylvania / Philadelphia
Overview of clinical drug development from final preclinical selection

Attend this seminar to design the most appropriate strategy for a clinical program, including all clinical developmental phases from IND to NDA/PLA.

By : Compliance online

2 May, 2016 - 3 May, 2016
Pennsylvania / Philadelphia