San Francisco QP Lunch & Learn
19th September | AC Hotel San Francisco Airport
San Francisco QP Lunch & Learn
19th September | AC Hotel San Francisco Airport
Join us for lunch, learning and networking
Location: AC Hotel by Marriott San Francisco Airport / Oyster Point Waterfront
Date: 19th September 2023
Time: 11:00am – 2:30pm PDT
Almac Clinical Services invites you to join our complimentary QP lunch and learn event where attendees will discover critical insights into our QP services. Experienced QPs, Olive McCormick and Caitriona Lenagh, will share their expertise and deliver interactive presentations on the subject.
This workshop will provide information on:
- Oversight of sites involved in the supply chain
- QP Involvement in Batch Document review
- Management and Oversight of Regulatory Submissions
Who should attend?
This workshop is perfect for those working within Clinical Supply, Regulatory, or Quality. As well as personnel within your organisations who support QP activities, or anyone interested in learning how their role impacts the QP certification process.
The date for this workshop has now passed, please get in touch with our team if you have any further queries.
Speakers
Olive McCormick
Head of Quality and QP, Almac Clinical Services
Caitrona Lenagh
QP Service Manager, Almac Clinical Services
Olive McCormick is the Head of Quality at Almac Clinical Services residing at the main headquarters in Craigavon, Northern Ireland. Olive is responsible for the QA, QC and the QP teams at this site.
With extensive industry experience spanning over 20 years, Olive McCormick’s expert knowledge and deep understanding of quality procedures has established her as a thought leader in the industry.
Caitriona Lenagh joined Almac in 2009 and has first-hand experience in all QP requirements in the world of Global Clinical Trials.
She has worked with global teams, educating, and mentoring them in the requirements of EU legislation, particularly the roles and responsibilities of the Qualified Person. She has extensive experience in a number of dosage forms and has performed audits of manufacturing, testing, and packaging sites throughout the world, imparting knowledge on regulatory requirements and industry expectations.