• Mar 19, 2021 from 9:30 to 11:00
  • Location: Online
  • Latest Activity: Jan 28

RSSL will be running a series of webinars over the next few months regarding key regulatory updates in the Pharmaceutical industry, hosted by Sue Mann.

Duration: 90 minutes Cost £150 (+ VAT)


19 Mar 21
14 May 21
16 Jul 21
20 Sep 21
08 Nov 21

These webinars are set to 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.

Regulatory changes continue despite the fact that over the last few months, most of our attention has been focused on dealing with issues arising from the COVID pandemic. There are a number of changes both within the UK as a result of Brexit planning, plus EU that will affect many if not all companies and it is important everyone is fully aware of upcoming changes so these can be planned and implemented within your organisation in a controlled manner.

There are also updates within the wider Pharmaceutical community, e.g. ICH, PIC/S, WHO, some of which may get overlooked as companies focus on local changes. This session will bring you right up to date with more recent announcements and provide more details on how you should manage these within your PQS or QMS and remain in compliance with GMP/GDP expectations.

There will be the opportunity to ask questions throughout the webinar which will be addressed in the live Q&A session.


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.

Learning Outcome

  • 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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