Inhalation drug product testing
Back to School - 15% Discount Offer
Available on all 2022 courses (except QP, RP and IRCA) booked by 31st October 2022
Diversity & Inclusion
CPD Hours: 35
IRCA CQI Accredited
This 5 day fully residential course, provides the most comprehensive training & certification for Auditors and Lead Auditor auditing GMP Pharmaceutical sites.
The course covers the role of an auditor to plan, conduct, report and follow up an audit of a pharmaceutical quality management system audit in accordance with ISO 19011. It gives you the skills to plan, conduct, report and follow up an audit of a pharmaceutical quality management system to establish conformance (or otherwise) against ICH Q10 and in accordance with ISO 19011. Learners will be assessed through practical tasks, activities and must also pass the IRCA PR325 written examination that lasts 2 hours.
By the end of the course you will:
We offer a number of discounts and specials offers on our training courses including Early-bird, Group booking, NHS and Seasonal discounts.
Peter is an experienced Pharmaceutical QA professional, with over 30 years GMP, ISO 9001 Quality Systems, audit and training experience.
Sue has worked in the industry for over 38 years, principally in quality and technical roles. She has a wealth of experience having held European Director & VP level positions at companies such as Eisai and Shire. For the last 11 years, Sue has been an independent consultant providing services across all major dosage forms and more recently ATMPs.
QMS lead auditor for the pharmaceutical industry
Fully accredited by IRCA and PQG, this is a highly customised Lead Auditor Training course that has been specifically developed for the pharmaceutical industry.