GOFARM – YOUR SPECIALIST IN PHARMACEUTICAL MEDICAL DEVICES
EXTERNAL R&D DEPARTMENT FOR YOUR COMPANY
Gofarm is a well-known and respected expert in the design, development and manufacture of “pharmaceutical” medical products – consisting of substances or mixtures of substances in various forms:
creams, gels, ointments, lozenges, tablets, capsules, drops and sprays.
We offer the first comprehensive R&D service for pharmaceutical medical devices in Poland,
i.e. from an idea to a finished product on the shelf!
With us, you can easily launch a new product on the market or adapt an existing one to new legal requirements.
Over 15 years on the market Gofarm has seen
over 400 formulations developed, including
over 50 medical devices in various classes and indications,
and 20 products transferred to higher classes.
CHOOSE THE SERVICE YOU ARE INTERESTED IN
AND FIND OUT MORE
CHANGE IN CLASSIFICATION OF MEDICAL DEVICES
(e.g. from Class I to a higher one)
BENEFIT FROM OUR EXPERTS’ SUPPORT
- Save time and resources – you do not need to have specialised knowledge and experience necessary to carry out complex research and development procedures
- Guarantee of efficient and fast processes
- Minimising project duration
- Comprehensive product care and access to the knowledge of experienced specialists
- Certainty that documentation will be adapted to current legal requirements
- Reliable support and advice
- Product ready for market, subjected to necessary procedures and certification
- Dedicated person responsible for regulatory compliance
- Convenience – you can delegate the mandatory, yet complex, procedures to our company and enjoy the results
The Gofarm laboratory is located in the Life Science Park of the Jagiellonian Centre of Innovation in Kraków.
The aforementioned services are conducted on the basis of the following legal basis: Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC