R&D Capabilities

Research and Development are vital components and essential to our company.

Chanelle Medical has thrived on the strength of our high quality science driven research and development programmes.  Our products are developed using our in-house expert scientists and with the assistance from our development laboratory in Amman, Jordan.

All R&D activities are thoroughly supported by Chanelle Medical Regulatory Affairs Department and subsequently supported by our Launch & Supply Teams.


Our R&D capabilities include:

  • Product synthesis
  • Formulation development: solutions, suspensions, powders, tablets & capsules including slow release formulations
  • Process Validation: pilot scale batches
  • Stability studies: protocols compiled according to ICH Guidelines
  • Bioequivalence studies: monitor & write Expert Reports
  • Registration dossiers: according to CTD format
  • Process Validation: commercial scale batches
  • Packaging of product
  • Consultancy service
  • Analytical development and validation

Regulatory Affairs

Chanelle Medical is a HPRA (Health Products Regulatory Authority) licensed company for the development and manufacture of medicines.

Joint Development

Chanelle Medical welcomes collaboration, the process of utilising knowledge by information sharing and the formation of agreements between research centres and companies.