Our experience provides a major head start. Besides ensuring continuous surveillance of evolving global and local legislation, as well as regulatory and cGMP requirements, our regulatory support specialists also author and maintain worldwide registration documentation.
- REACH registration
- Expertise in registration processes worldwide
- Know-how in regional regulatory specifics
- Proactive implementation of new regulatory requirements
- Creation of Drug Master Files
- Creation and maintenance of Certificates of Suitability
- Consultancy in regulatory issues
- Regulatory affairs services
SIGN IN TO OUR ONCARE WEB PORTAL
Register for our onCare web portal to get 24/7 access to standard regulatory documents (such as EIP product regulatory datasheets, summaries of safety data, storage stability data, reduced frequency testing data) online.