European Regulatory Affairs Limited can provide Regulatory Affairs Overview Training to all interested parties.
For Junior officers this will provide an insight into the function of Regulatory Affairs, why it is necessary, what is required to support the Regulatory function and what Regulatory Affairs departments need from other departments to make projects a success.
For Seniors this will provide detailed training on Module 3, Regulatory Strategy as well as comprehensive, specialised training in all aspects of the EU and UK legislation and in the MRP/DCP/CP and eCTD systems for registering medicines in the EU/UK, which is our speciality.
- Full text notes including suggested wording for certain sections of the dossier
- Case studies tailored to your level of knowledge
- All relevant and current guidelines for each section