Diapharm supports pharmaceutical companies in all medical and scientific tasks. We see ourselves as a complete service provider for medical affairs when it comes to medical writing and expanding medical knowledge.
The Diapharm team for medical affairs presents information on medicinal products in the form it needs to be: as expert reports, medical statements or as CTD modules 2.4 to 2.7 for marketing authorisation documents, to name just a few examples.
Diapharm’s medical writers prepare all the documents for pre-clinical tests and clinical studies. On request, we can help manage clinical studies in close cooperation with a CRO and develop the accompanying study documentation.
When it comes to medical information, we process medical enquiries from doctors, pharmacists and patients on our clients’ behalf – 24 hours a day, 365 days a year (24/7), if need be.
In our role as information officer and/or service provider, we take a close look at whether packaging, sales and marketing texts comply with marketing authorisation documents as well as additional requirements, such as the German law on drug advertising (HWG).