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CPD Hours: 2
Online
These webinars highlight key regulatory updates covering UK guidance (specifically GMP & GDP), EU general guidance and approaches being taken by UK MHRA. QA professional will be able to better navigate through the different sources of information that is currently published and gain understanding of the implications of changes to Pharmaceutical Quality Systems in an organisation.
By attending this event you will learn:
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Special offer
We offer a number of discounts and specials offers on our training courses including Group booking, NHS and Seasonal discounts.
Sue Mann
Sue has run her own consultancy since 2009 and works with companies all around the world. She became a QP in the mid 1980’s and a QP Assessor in the early 2000’s. Although her core knowledge and experience is in GMP, she has built up knowledge and experience in Good Distribution Practice (GDP) and has helped write a guidance document published by PQG and ECA which expands upon the EU GDP Guideline. Sue has dealt with many GMP systems in her over 40 years’ experience in the industry; including WHO whilst involved in a development project in a number of African countries, funded by UNIDO. Sue has been a QP for many years and understands the complexity of the role and its position within a company. She is an inspiring trainer being able to break down complex topics into understandable sections and can “train” at all levels in an organisation. She understands what it is that is important in fulfilling the role of a QP.
Related course
QP law and administration
Provides a thorough knowledge and understanding of European and UK Laws related to the manufacture and distribution of medicinal products for human and veterinary use