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Laboratory Compliance Conferences

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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
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
Equipment Calibration, Maintenance, and Validation: What Auditors Look for in a Controlled Process- WEBINAR

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
Understanding Disinfectant Qualification Studies – How to Avoid Errors (WEBINAR)

This webinar on Disinfectant Qualification Studies will teach you disinfectant testing methodologies, provide examples of disinfectant efficacy tests and show how to troubleshoot problems related to disinfectant efficacy testing.

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

> 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