Catapult is building up to become a GMP manufacturing partner, a CDMO. Catapult has clean room facilities, storage rooms, including a qualified cooling room, procedures for labeling and packaging, and equipment for cleaning and sterilization. Two classified suites will be available from January 2021. We are in the establishing phase for small scale manufacturing, including formulation, fill & finish. Our quality system is according to GMP, but a compliance check may be performed for other regulatory standards if needed.

  • 2 Clean room suites
  • Qualified cold room storage
  • Equipment for cleaning and sterilization