WEBINAR: Tuesday July 28th, 2020, 9.30am - 11.30pm EDT , Cost $275 CDN plus HST

Are you getting the most from your Self Inspection (Internal Audit) Program?

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

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

This 2 hour webinar offers advice on how to get the most from your self inspection (Internal audit) program 

WEBINAR: Tuesday August 11th, 2020, 9.30 am - 11.30pm EDT , Cost $275 CDN plus HST

Preparing and Understanding the Method Transfer Process (For QA Personnel)

Failures during method transfer continue to be a burden in the pharmaceutical industry, in particular for Importers/Distributors. 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 the labs are generally extremely competent. So why do we still have problems?

This 2 hour webinar explains the process of method transfer from a non technical perspective for QA staff in a way 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 August 18th, 2020, 9.00 am - 11.30pm EDT , Cost $355 CDN plus HST

Laboratory Transfer of Analytical Procedures - Integrating Future Philosophies into Current Practice

When you try to transfer analytical procedures, is it frustrating and time consuming? Do methods which have been transferred still give issues in routine use? Would you like your procedures to be more robust with fewer problems throughout their lifecycle?

If you answered yes to any of these questions, then this webinar is for you.

In this 2.5 hour webinar, modern concepts such as QbD philosophies i.e risk assessment and method understanding are combined with our current practices to ensure a smoother method transfer process, a more robust performance, leading to fewer OOS results due to the procedure in routine use.

Next Date: 28th of October , 2020, Exact Location TBD. 

Note: Dates may be adjusted due to covid 19 travel restrictions Please register your interest by email or select the pay by invoice option. No invoices will be billed until the course has been confirmed. 

This one day course is designed to provide essential training for conducting Out of Specification (OOS) investigations in the laboratory (Phase 1). 

 UK, exact location to be determined. Next Dates: Thursday 29th and Friday 30th October, 2020

Note dates may be adjusted due to covid 19 travel restrictions Please register your interest by email or select the pay by invoice option. No invoices will be billed until the course has been confirmed. 

Lifecycle Management focuses on value added activities during development and validation and which leads to higher success rates when applied to the transfer, verification and routine use of analytical procedures. It also integrates the management of procedures into current quality systems to ensure ongoing acceptable performance of procedures, regardless of the end user location.

 Next dates November 10th (Tues) and 11th (Wed) 2020.  Near Toronto Airport , Cost $1120 CDN plus HST

Limited Spaces Available

Note:  Dates may be adjusted due to covid 19 travel restrictions Please register your interest by selecting the pay by invoice option. No invoices will be billed until the course has been confirmed. 

Lifecycle Management focuses on value added activities during development and validation and which leads to higher success rates when applied to the transfer, verification and routine use of analytical procedures. It also integrates the management of procedures into current quality systems to ensure ongoing acceptable performance of procedures, regardless of the end user location.

Next Date: Tuesday November 17th, 2020. Near Toronto Airport , Cost $620 CDN plus HST

Note:  Dates may be adjusted due to covid 19 travel restrictions Please register your interest by selecting the pay by invoice option. No invoices will be billed until the course has been confirmed. 

This one day course is designed to provide essential training for conducting Out of Specification (OOS) investigations in the laboratory (Phase 1).