Quality Control Testing

Farmalyse performs pharmacopoeial and non-pharmacopoeial tests routinely on a large scale basis for pharmaceutical products and medical devices in compliance with GMP-GCLP.

All our tests are based on the concept of a one-stop-shop.

We combine chemical and microbial product knowledge with quality control testing, method development and validation studies for finished formulations, active pharmaceutical ingredients (APIs), excipients and medical devices.

Through our state-of-the-art laboratories we offer a complete range of services including chromatography facilities (HPLC, UPLC, GC, LC-MS and TLC), spectroscopy (UV and IR) dissolution testing and GMP certified class A – D clean rooms.

Standard throughput times are between ten and 15 working days. Express services can also be performed in three to five working days based on individual requirements.

Farmalyse is currently evaluating and devising rapid analysis techniques through which the standard throughput time is reduced by three to five times. Please contact us for more information.