The Product Information is the scientific business card of a pharmaceutical product, promoting the quality, efficacy, and safety of pharmaceutical products.
Its translation into accurate and up to date information or promotional material is a key responsibility of a RIP, but it is only the visible part of many RIP duties to be conducted in close collaboration with notably Regulatory Affairs to ensure full compliance with regulations and laws.
RIP acronym stands for Responsible person for Information and Publicity. Each Marketing Authorization Holder (MAH) active in Belgium must appoint a RIP.
There are circumstances where RIP and Regulatory Affairs (RA) department should work closely together. Here are non-exhaustive examples of it:
Q-support can provide you with an experienced, pragmatical and efficient Responsible person for Information and Publicity for your company.
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