Insights
Tepnel Case Studies – Method Development for Peptide Drug Products
Tepnel is a GMP quality assured analytical testing facility, with over 30 years of expertise and...
Microbial Examinations of Non-sterile Products
Microbial contamination can present a number of problems when it comes to pharmaceutical...
What does Brexit mean for Pharmaceutical Manufacturers?
Get in touchIs the clock now ticking for European Pharmaceutical manufacturers to select their Lot...
Enhanced Approach to Method Development Meets Regulatory Expectations and Provides Added-Value to Clients
At Tepnel, we have over 40 years of experience in the pharmaceutical field. Focussing on...
USP <787> Small Volume Sub-visible Particle Testing
Tepnel is excited to announce that the small volume sub-visible particle adaptor for our HIAC...
Forced Degradation Studies
Does your new or existing drug product filing come under ANVISA Resolution RDC-53 and require...
Inhaled Cannabinoid Development
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Closed Container Integrity Testing (CCIT)
Product quality, safety and sterility testing methods and technologies have evolved, Tepnel can...
Thinking about a new career opportunity?
We've currently got have no open vacancies available to join our team in quality control testing...
Addressing Medicine Supply Chain Shortages due to the COVID-19 Pandemic
The continued availability of medicines is one of the most important priorities for EU authorities...
Remote Auditing for GMP Compliance
The impact of the Covid-19 pandemic on GxP supply chains and the lockdown measures mandated by the...
Tepnel Pharma Services Limited announces the completion of the Asset Transfer from Hologic Ltd.
On 4th March 2020, the transfer of the business and assets of the Tepnel Pharma Services brand of...
Tepnel Pharma Services introduces Accelerated Stability Assessment Programme (ASAP) to its Stability Testing Portfolio
Stability studies are a time consuming and resource intensive task during the development of new...
Tepnel Pharma Services have invested in Fusion QbD software
Quality by Design (QbD) is a systematic approach to development that begins with setting a...
MRA comes into force between the FDA and the EU
The first of November 2017 has become a notable and unprecedented date in the history of medicines...
