• non-clinical development
• clinical development
• marketing authorisation and certification
• existing marketing authorisations
• medical devices

i.DRAS stands for international, individual,  innovative and intelligent solutions for your development, registration and marketing authorisation project.

i.DRAS is your partner for marketing authorisation and registration projects concerning human and veterinary medicinal products from the preclinical and early clinical phase to the submission of the MA dossier to the point of all regulatory post-marketing or post-registration activities. We also see ourselves as your professional partner for the complete life cycle of your product. The same applies to borderline medical devices and medical devices incorporating an ancillary drug substance. Our services for you may be of very different natures - limited to consulting only, comprising small parts of a project or the responsible management of entire projects - depending on the scope you request.

 

• glossary
• imprint

i.DRAS GmbH · Fraunhoferstraße 18b · D-82152 Planegg / Martinsried