Clinical Trial Service

“Special medications demand special handling”

Compliance with GMP guidelines is not only a statutory requirement but also an important safety factor for test subjects, clinical investigators and sponsors.

The correct packaging design, the correct packing and the timely delivery of clinical samples contribute significantly to the success of a clinical study.
Our experience in the area of manufacturing clinical trial medications makes us a reliable and competent partner for your special requirements.

The corresponding GMP certification, our technical infrastructure and our trained personnel enable us to package your study medications for clinical trials in phases I – IV.

Secondary packing of clinical test samples is performed manually. The principle of dual control is vigilantly maintained, and regular in-process checks of these “hand-picked” samples guarantee maximum safety and quality.

We focus on the challenge of flexibly and rapidly implementing your individual requirements in accordance with current GMP guidelines and offer ourselves to you as a partner in matters of packaging clinical test samples.

Contact:
DI Dr. Helena Salapovic, h.salapovic et mono.co.at    Tel.: +43-(0)1-330 0671-15
Mag. Dr. Michaela Freiler, m.freile et mono.co.at    Tel.: +43-(0)1-330 0671-61