Regulatory affairs

We may assist you with the following services:

• Advice on authorisation strategies
• Adaptation of the EU dossier to the requirements of Switzerland (Module 1)
• Implementation of registration procedures from ‘pre-submission’ to ‘post approval’ 
  
• Life cycle management (variations, renewals)
• Adaptation of packaging texts and medicinal product information texts

Would you like to receive a quote? We will gladly take time for your needs and evaluate possible solutions together with you. You are welcome to send your enquiry to our e-mail contact phrmsrvcsllgch.