DeSia a specialized consultancy in Regulatory, Quality, and Clinical Affairs, offering expert support for all technical documentation needed to achieve CE certification for both medical devices and in vitro diagnostic devices.

You can easily get reliable and cost-effective services from a single trusted provider:
STED, PMS, PSUR, Usability, CEP & CER, BEP & BER, PMCF, SSCP, 
Clinical Trial Protocol, Investigator Brochure, Case Report Form, 
Software Validation, Process Validation, and Transport Validation with transport simulation testing.

DeSia

Basak Baranoglu Demirci

This department is responsible for creating and managing documents that communicate scientific and medical information, ensuring clarity and compliance with regulatory standards.

Medical Writing

This department manages the strategic and operational aspects of clinical programs and initiatives.

DeSia

Org chart

Teams

Medical Writing

Clinical Affairs

Offices