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Synoptis Pharma

We are a dynamically developing technological company. We produce and register pharmaceuticals using our key competences.

Our key competences include:

Assuring and controlling quality (QA/QC)

We cooperate only with the production plants that in care for the highest quality and safety of their products have implemented GMP, HACCP, GHP or ISO, depending on the status of the product made. We monitor the production processes through the suppliers qualification and quality audits conducted at their premises.

We test all our products prior to the market launch. We care for the quality and safety of the products offered in their entire durability periods therefore we conduct the stability tests – also for the dietary supplements and other foodstuff.


The R&D Department is responsible for the refund of our products. The department prepares the necessary documentation, motions for the setting of the official price and for the inclusion into the lists of reimbursed drugs.


High class specialists are responsible for the registration of our products ensuring the requirements of adequate offices: Main Sanitary Inspectorate and The Office for Registration of Medicinal Products, Medical Devices and Biocidal Products are fulfilled.

The medicinal products, dietary supplements and medical devices’ documentation is prepared inline with the legal requirements, both Polish and European. Medicinal Products are registered according to the national and European procedures.


Caring for patients’ health and safety we fulfil the duties regarding pharmacovigilence. We act inline with the adequate procedures. Our staff collects, assesses and draws conclusions from the possibly reported adverse drug reaction to constantly monitor the benefits-risk ratio of our medicinal products.

We support independent pharmacies


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