Key regulatory updates for the pharma industry

90.00 Minutes

CPD Hours: 2


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.

This webinar is ideal for anyone working in operational quality, quality systems and quality compliance roles, Qualified Persons (QPs), trainee QPs, Responsible Persons (RP) and those in Regulatory Affairs who are interested to know if any changes will affect them. It can also be of benefit to Quality Control and supply chain colleagues.
The topics covered in each webinar are based on latest regulatory and industry aspects.

    By attending this event you will learn:

    • Keep up to date with current regulatory expectations
    • The flexibilities associated with both GMP and GDP
    • Understand what you must do to remain in compliance with GMDP expectations always

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Helping your training budget go further

We offer a number of discounts and specials offers on our training courses including Group booking, NHS and Seasonal discounts.

Meet the tutors

Sue Mann

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.

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