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.

 

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