Our client, a global mid-sized pharmaceutical company operating in some 80+ countries and providing 1,500+ products across multiple therapeutic areas was seeking a collaborative partner to provide both onsite and offshore resources to support them with numerous Regulatory activities including publishing and data management.
Read our latest case study and learn how Navitas Life Sciences have successfully provided a team of dedicated resources, serving as an extension to our client’s Regulatory Affairs team, to support their technical and publishing operations. Our client is now benefiting from:
- 0% technical rejections from Health Authorities
- 100% adherence to SLAs
- High productivity with a low turnaround time
- Successful delivery of 100+ submissions in the EU
Please complete the form to download our case study.