Social Drop in Session: Monday April 27th , 2020, 10.00am EDT (Duration 15 to 20 minutes)

Start your week on a positive note , breathe and give your brain a boost! This is a free social session and it includes some brain exercises, trivia, fun facts and things to make you smile. We hope to boost those grey cells, make you laugh and not feel so alone! 10.00am EDT (Duration 15 to 20 minutes). All ages welcome!

WEBINAR: Tuesday May 12th, 2020, 11 am - 12.30pm EDT (Duration 1.5hrs)

Preparing and Understanding Method Transfer for Importers

Failures during method transfer continue to be a burden in the pharmaceutical industry, in particular for Importers. The country from which we import the drug states the analytical procedure had been validated. Our contract testing labs are approved by our government agencies to test these products and they are generally extremely competent. So why do we still have problems?

This webinar explains the process of method transfer from a non technical perspective for QA importers that can help you communicate with the testing laboratories to improve the success rate of method transfers and gain an understanding of your procedure and the transfer process.

WEBINAR: Tuesday 19th May, 2020, 11.00am-12.30pm EDT (Duration 1.5 hrs)

Enhanced Approach Versus Traditional Approach for Analytical Procedures.

What’s the Difference?

The simple answer is that the Traditional Approach refers to what we have been doing for years. The Enhanced Approach considers and integrates the key concepts and strategies of QbD and Lifecycle management.

There are significant differences in the two approaches. One of the major ones is that the Enhanced Approach requires a different mindset and requires a shift of focus onto the quality of the data generated by the procedure rather than being on the procedure itself. Although it requires more work upfront, the enhanced approach does result in more robust methods throughout their period of use.
This webinar summarises and discusses the differences between the two approaches. I hope you can join us!

WEBINAR: Thursday May 21st, 2020, 11am - 12.30pm EDT (Duration 1.5hrs)

Are you getting the most from your Self Inspection Program?

Most companies check the compliance box and meet the regulatory requirement to have a self inspection program in place. It is designed only to monitor compliance with current GMP regulations and SOPs. More often than not it happens once a year and bogs down QA resources. It can do so much more!!

In actual fact the self inspection program is one the most powerful tools you have in your Quality Management System toolbox. Unfortunately, I find it is seldom set up to its maximum potential.

This webinar offers advice on how to get the most from your self inspection program