Writing a GDP Training Programme: What does this mean in practice? Chapter 2 of the EU GDP Guidelines requires a written training programme. But what exactly does this mean and how can it be put into practice?
If you are a responsible person, how do you keep abreast of all the changing rules and regulations, whilst fulfilling the requirements of your role? Come and join us for our inaugural monthly RP forum, Meet other RPs, and join a discussion of a hot topic. The first topic will be “Inspections: what to inspect” on 11th January. See the full program on our website.
Are you working in an environment where you need to comply with Good Distribution Practice (GDP), and if so, is everyone in your team aware of the guidelines and how they apply? We can provide training at every level for every function, so why not take a look at our offerings…
The Future of Medical Device Regulation in the UK- Do you know that the regulatory framework for the manufacture and supply of medical devices in the UK is changing?
The Future of Medical Device Regulation, on the 16th of September, the Medicines and Healthcare products Regulatory Agency (MHRA) launched a 10- week