Focus on the things you can change and let go of the things you can’t. At Tepnel we focus on the provision of pharmaceutical testing in support of drug development with an emphasis on ICH stability testing, UK and EU product testing and ICH method development and validation for inhalation, oral dosage, parenteral and peptide formulations. Our people are committed to providing laboratory services that deliver on the promise of price, innovation and quality through an experienced team and a strong outcome focussed culture. Our cGMP pharmaceutical testing facility is located in Scotland, UK where we work together collaboratively with our partners by doing the things that let you focus on the things you need to do.
ICH method validation for a variety of analytical techniqeus, for example stability indicating assays.
40 years plus of supporting stability testing on tablets, capsules, parenteral, lyophilised and inhaled formulations.
Accurate assessment of product stability and shelf life are key to the successful development of a potential drug substance or finished product. Ever increasing demands for data integrity coupled with the milestones of product registration necessitate the need to have reliable, approachable and focused supplier. At Tepnel we understand your needs as a customer to have a pro-active, flexible and reliable support service that allows you to focus on the value added activities within the manufacturing supply chain.
Analytical method development for analytical techniques such as HPLC, microbiological and ELISA based applications.
Sterile and non-sterile regulatory compliant microbiological testing including bioburden, absence of pathogens, sterility, bacterial endotoxin testing, microbiological assay and preservative efficacy testing.
UK and EU product/batch release testing
cGMP QC analytical testing on tablets, capsules, parenteral and lyophilised products.
cGMP support for inhaled formulations and medical devices.
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