Research Connect: Clinical Trials Preparation for Regulatory Inspection and Audits – Part II-Q&A with Experts – Dec. 14, 2022

Session Description

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Research Connect is delighted to invite you to the Part II session of “Clinical Trials Preparation for Regulatory Inspection and Audits Part II-Q&A with Experts”. On Nov 23rd we hosted the first part of this webinar and received over 500 registration requests, but due to lack of time, we were unable to dedicate sufficient time to Q&A. We are pleased to inform you that both Julie Lipszyc and Flora Noitsis have agreed to join us for the Part II session to dedicate time to answer all questions.

To facilitate a more productive session, you can submit questions in advance to RCSS@hhsc.ca, and of course you can raise questions during the session as well. Given the nature of the webinar we anticipate reaching full capacity again, therefore, we encourage everyone to register as soon as possible.

This will be our last webinar for 2022. A short reflective survey will be sent out to everyone and we welcome and encourage everyone to help us evaluate our progress in 2022 as we plan our 2023 journey.

Special highlight on the guest panelists:

Flora Noitsis: Flora has recently retired from Health Canada where she served as a Specialist & GCP Inspector. During her 30 years of service with Health Canada, Flora planned and conducted inspections and investigations of the compliance of sponsors, investigators and establishments within Canadian Good Clinical Practices regulations and guidelines. She is currently working as a Senior Associate, Operations & Compliance, at BioAcuity Consulting Inc.

Julie-Léa Lipszyc: Vice-President, Quality & Compliance at BioAquity Consulting, has over 25 years of experience in the pharmaceutical and biotechnology sectors. Julie-Lea has a technical diploma in Biophysics and a Master’s Degree in Sciences and Technology in Quality Assurance of pharmaceutical, cosmetic and dietetic from the Pharmacy University of Paris XI.

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