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Regulatory Affairs

In a rapidly evolving space in the sector, Compass Life Sciences understand that evolving regulatory environments are directly linked to regionally and internationally shifting demands from the regulators, successfully bringing a new treatment or device to market is more complex than ever before. 

We strive to share our broad experience and knowledge to bring consultative solutions bringing talent to the table.  Equally our network of candidates from across the sector gives us real insights in to the ever changing demands being faced by the industry, which we seek to address by introducing the right talent with the right experience in highly complex roles. 

Considering new skill areas such as experience working with ATMPs, PIPs, Orphan applications, and other regulations which require specialist knowledge, we are well integrated with both clients and candidates working in traditional and cutting edge areas of Regulatory Affairs.

Example role types include:

  • Clinical and Development Regulatory Affairs
  • Regulatory Writing and Labelling
  • Regulatory CMC
  • Submissions and Regulatory Publishing
  • Lifecycle Management
  • Medical Device Management

To view Compass Life Sciences’ other Specialisms, please click here.

Regulatory Affairs News