LIFECYCLE-AS-A-SERVICE
Market authorization is only the beginning: We accompany you through the complete life cycle of your product – from maintenance of the authorization to further product development.
Once your pharmaceutical has been successfully registered for the EU, the European Economic Area or the Swiss market, the next steps are not only the marketing of the product, but also the maintenance and preservation of the marketing authorization. In case of corresponding adjustments or further developments, you will be faced with further tasks and requirements.
To allow you to continue to focus on your product alongside all the requirements from the authorities, we handle the regulatory part. In particular, we take care of…