Sometimes matrix approach to cleaning validation has gaps or even worse customer or 483 audit findings due to the program's near impossibility to manage....   Find out more

If a 483 is received knowing how to respond will lessen chances of receiving a Warning Letter....   Find out more

It will discuss possible future actions by FDA and by the US laboratory community and assess their probability....   Find out more

Are you in compliance with the FDA regulations for Cleaning Validations of your manufacturing equipment?...   Find out more

Participants will understand - Is validation a regulated activity? When to pull the trigger for validation? Importance of suitability testing....   Find out more

This live webinar training will provide a clear process for compliant laboratory OOS investigations....   Find out more

You’ll learn the benefits and impacts of validation and how it can benefit your customers and your business....   Find out more

This webinar will help attendees understand the instrument qualification and system validation processes....   Find out more

This webinar will give a good understanding of FDA requirements for training and provide recommendations for implementation....   Find out more