Class D Clean Room Environment now available for Sterility Testing
The sterility of a pharmaceutical product is defined by the absence of viable and actively multiplying micro-organisms when tested in specified culture media. Sterility testing is performed on the end product and is one of the quality control tests specified for release of a batch of sterile product.
The new 22 Sq meter Sterility Suite offered by the team at Tepnel offers two Class A isolators in a Class D room.
Using gaseous sterilisation within these isolators means that our sterility testing services are conducted in an environment free from microbial contamination. Giving you the added assurance that the testing is conducted in a completely sterile environment as preferred by Regulatory Authorities and QPs.
To discuss your project requirements contact Business Development Manager, Stewart Neithercut: email@example.com or call: +44 (0)7785 438 308
Why choose Tepnel for Sterility Testing?
- An experienced team of dedicated, trained personnel who test multiple batches on a daily basis
- Isolator technology, reducing the risk of false positives
- Gaseous sterilisation, reducing the inherent risk of contamination – giving additional confidence in the results.