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Laboratory Compliance Conferences

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>Conference documentation and webinars for this Sector

Understanding and Implementing ISO 17025

This webinar will provide a detailed information on the critical requirements of ISO 17025 and recommendations for cost effective implementation. You will learn steps towards laboratory accreditation and how to prepare for an ISO 17025 audit.

By : Compliance Online
Product Type : On Demand Webinar
Calibration and Qualification in Analytical Laboratories Webinar

This webinar will provide a detailed understanding about calibration and qualification of laboratory equipments, development of a qualification master plan, allocation of equipments to qualification categories A, B, C, and the approach for qualifying existing systems.

By : Compliance Online
Product Type : On Demand Webinar
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
Solutions for Addressing Fungal and Bacterial Spore Outbreaks in Pharmaceutical- Webinar

This webinar will discuss how personnel practices, transferring items into cleanrooms, facility design, construction, and sporicidal chemistries are critical and how it can be addressed in developing a successful contamination control program.

By : Compliance Online
Product Type : On Demand Webinar

> Previous Conferences, Webinars and Training All Past Conferences >

Quality Control for Microbiological Media and Reagents

Learn to develop appropriate quality control practices to evaluate the acceptability of media and reagents for laboratory use.

By : Compliance online

22 Dec, 2015 - 22 Dec, 2015
California / Palo Alto
Best Practices for an Effective Cleaning Validation Program

The program will describe the requirements for establishing an effective cleaning validation program, including the development of a general policy, a “Cleaning Validation Master Plan” and the appropriate documentation for each study to be performed.

By : Redstone Consultants

8 Dec, 2015 - 8 Dec, 2015
New York / New York
Analytical Instrument Qualification and System Validation

This webinar will help attendees understand the instrument qualification and system validation processes and will provide instruction on how to prepare for FDA audits and how to become part 11 compliant.

By : Redstone Consultants

24 Nov, 2015 - 24 Nov, 2015
New York / New York