Pharmacovigilance requirements for UK authorised products webinar recording, which took place on 13 January 2020. This webinar was part of a series of Brexit and post-transition guidance webinars.
Post-transition: Pharmacovigilance requirements for UK authorised products webinar recording, which took place on 22 October 2020. This webinar was part of a series of EU Exit and post-transition guidance webinars.
The BPC is looking to appoint a new Chair from October 2021. The current Chair, Professor Kevin Taylor, shares some of the highlights and achievements of the past 8 years, and we launch the process of finding his successor.
In part 1 of the inspectorate recruitment posts, we provided information on the inspector role and recruitment process, part 2 provides more information on the benefits and opportunities available to MHRA inspectors.
Have you ever thought about becoming an MHRA inspector but wanted to know more about the role, the application process, or the benefits associated with joining a talented and dynamic team protecting public health? Part one of this two-part blog will hopefully give you the information you need to consider for applying for future roles.
The GXP environment is evolving as digital technologies are increasingly being applied to the development and manufacture of medicines.
This month sees the close of the consultation on the application of Analytical Quality by Design to pharmacopoeial standards. We sat down with Peter and Stephen, pharmacopoeial scientists for the British Pharmacopoeia, to discuss why this consultation may prove vital …
Sharing experience from recent events to help you safeguard the legitimate supply chain and avoid risks to public health
The definition of a falsified medicine and how to check that your systems comply
Implementation of the FMD safety features in the UK