Martina Cugovčan
About Martina Cugovčan
Martina Cugovčan is a Regulatory Affairs Associate at Dechra Pharmaceuticals Plc, where she has worked since 2013. She specializes in registration dossier submissions for pharmaceuticals across various international markets.
Work at Dechra Pharmaceuticals
Martina Cugovčan has been employed at Dechra Pharmaceuticals Plc since 2013, serving as a Regulatory Affairs Associate. In this role, she manages registration dossiers, renewal, and variation submissions for pharmaceuticals. Her responsibilities include ensuring compliance with regulatory requirements for pharmaceutical products in various international markets. Based in Northwich, Cheshire, United Kingdom, she has contributed to the company's operations for 11 years.
Regulatory Affairs Responsibilities
In her position, Cugovčan is responsible for the registration of pharmaceuticals in multiple international markets, including Croatia, Russia, Ukraine, Greece, and Azerbaijan. She prepares expert reports specifically for Part II of the EU dossier, which is essential for the regulatory approval process. Additionally, she is involved in preparing documentation for change controls related to pharmaceutical registrations, ensuring that all submissions meet the necessary regulatory standards.
Previous Experience at Farmal D.d.
Before joining Dechra Pharmaceuticals, Martina Cugovčan worked at Farmal D.d. as an Analyst in the Quality Control of Drugs from 2009 to 2013. During her four years in this role, she gained valuable experience in quality assurance processes and regulatory compliance within the pharmaceutical industry. This background has contributed to her expertise in regulatory affairs.
Education and Expertise
While specific details about Martina Cugovčan's educational background are not provided, her extensive experience in regulatory affairs and quality control indicates a strong foundation in pharmaceutical regulations and compliance. Her role requires a thorough understanding of international regulatory frameworks and the ability to prepare detailed documentation for pharmaceutical products.