Drug development support

Drug product development support is the pillar of SYNAVIA consultancy service. Thanks to our solid hands-on experience from both pharmaceutical and clinical development we are able to provide scientific as well as regulatory input for your drug development planning and enhance your chances at solving various development issues.

In every task, we focus on clear identification of the “end-user” of our services, i.e. regulatory agency, therefore it is our priority to translate the perspective of pharmaceutical companies into the regulatory way of thinking.

Pharmaceutical development / Quality / CMC

We are ready to support your pharmaceutical development process, leveraging our scientific, industrial and regulatory expertise to guide you to a successful marketing authorization. More

Clinical development

Design and careful planning helps you conduct your clinical studies efficiently. We have 20 years of experience in creating lean clinical development programs to generate missing clinical evidence for registration of Gx and Value Added Medicines and have gained considerable expertise in it. More

Regulatory science & strategy