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Compliance with GMP regulations is not only a legal prerequisite for the production of study medication, but also an important safety factor for test persons, clinical investigators and clients. The right packaging design, correct assembly and timely delivery of clinical trial samples are essential to the success of a clinical trial.

EXPERIENCE Our experience in the production of clinical trial medication makes us a reliable and competent partner for your particular needs. The relevant GMP certification, our technical infrastructure and our trained staff facilitate the assembly of your study medication for clinical phases I – IV. The secondary packaging of the clinical trial samples is carried out by hand. The continuously observed dual control principle and regular in-process checks of ‘hand-picked’ test samples guarantee maximum safety and quality. We take the task of flexibly and quickly implementing your individual requirements in accordance with the current GMP guidelines very seriously and would welcome the opportunity to assist you as a partner for the assembly of clinical trial samples.

If you are interested to take advantage of our services, please contact:
projects@mono.co.at
Tel: +43-(0)1-330 0671-0

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