People. Progressive. Principled

CPhI Worldwide 2017

At Tepnel, we believe that it is our responsibility to provide our customers with high quality, regulatory compliant data.

For holders of a Manufacturer’s Authorisation for IMPs (MIA(IMP)), our IMP QC release testing services cover a range of formulations; oral dosage, parenteral, complex peptide and inhalation products. We also specialise in formulations that require both chemical and microbiology testing. 

If you would like to speak to one of the team about how Tepnel can build efficiencies to help drive down your outsourcing budget, visit stand 61D32 or call us on +44 (0)1506 424270 



Why should you talk to Tepnel ? 

  • We have over 20 years’ experience in batch release testing for a wide range of pharmaceutical companies.
  • Our cGMP compliant facilities are located in Scotland, UK part of an innovative and world recognised Life Sciences Destination.
  • We service a wide range of formulation types.
  • We have particular experience in tablets/capsules, parenteral, inhaled and complex peptide formulations.
  • Our laboratories cater for both chemical and microbiological analysis.
  • We can handle Schedule 1 through 4 licenced plus OEB/OEL category 2/3 materials.

Our Commitment to you

Tepnel’s Triple A seal ensures Accountability, Affordability and Adaptability on all your IMP release testing requirements. As an advocate of Vested Outsourcing our focus is on delivering outcomes that add economic value.


Free Stability Storage for Life & T0…. For your unique code please provide your details:

Your Name

Your company (required)

Your Email (required)

Your Message

This form collects your name, Company name and email address and we may use these details in the future to contact you regarding our products and services. Please read our privacy policy for full details on how we protect and manage your data.

I consent to Tepnel Pharma Services collecting my details and contacting me regarding its products and services.