There are few industries as heavily regulated as Pharmaceuticals and Biotechnology. There is a wealth of guidelines, codes of practice and regulations covering every aspect of the business of clinical trials; this is also true of clinical meetings. Our internal compliance team work with ensure that our staff are fully trained on current best practice for clinical meetings and they keep records of individual clients internal policies which are available to our event teams.
GENERAL GUIDELINES
Since 2007, IFPMA and subsequently local guidelines, have become much more stringent, with the perception of meetings involving Health Professionals being very much in the forefront. Each region, and indeed, country has their own interpretation of those given by IFPMA, and in some cases have become even more rigorous in their approach to the locations, venues and how much time should be spent by Health Professionals at each event. MD Events has a database detailing a plethora of local guidelines to ensure you are informed of the latest updates and advice on keeping your event within the relevant regulations.
