This video provides information on procedures to be followed on the arrival of equipment before using for patient reporting, including Installation Qualification, Operational Qualification and Performance Qualification.

This video provides information on procedures to be followed on the arrival of equipment before using for patient reporting, including Installation Qualification, Operational Qualification and Performance Qualification.

This video highlights the importance of equipment management, essential pre-requisites, equipment purchase, pre-purchase planning.

This video highlights the importance of equipment management, essential pre-requisites, equipment purchase, pre-purchase planning.

This webinar demonstrats the features and requirements of Computer System Validation (CSV) process and why it is important for companies operation in process industry.

When do you have electronic registrations and signatures and thus need to be in compliance with Part 11

How to Validate Computerized GxP Systems in the Life Sciences.

Recorded voice over for the presentation entitled FDA Trends: New Validation Strategies at the 2nd International Conference on Continued and On-Going Process Verification, 20th March 2017, Novotel Hamburg, Germany.

If you conduct process validation, you need to ensure that your results are valid. Beyond the regulatory requirements, statistical approaches will help you achieve the desired result - processes that produce only conforming material.

This Video provides an overview of the FDA's Drug Development Process. This webinar also includes the major FDA regulations involved in the Drug Development Process - the GLP, GMP and GCP regulations.