Services
EuroPharMedTech specializes in Market Access, Pharmacovigilance, Training, Medical and Technical Writing, Medical Affairs, Medical Information and Publicity, and Data Computing, delivering integrated solutions to advance pharmaceutical innovation.
MARKET ACCESS
Market access may prove to be a challenging task for your team, but EuroPharMedTech is able to provide the right experts with the right network for a successful product.
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CLEVAIR-HTA
An innovative approach to HTA and Healthcare Market Access, powered by our partner CLEVAIR.
Through the use of Artificial Intelligence and precision analytics, CLEVAIR delivers solutions that enhance quality, boost productivity, and generate new strategic insights — tailored specifically for pharmaceutical teams.​​​
EU AI Act
EuroPharMedTech (EPMT) provides specialized AI assessment and compliance solutions designed for pharmaceutical SMEs. Our services help organizations align with the EU AI Act, ensuring that their AI systems meet ethical, legal, and regulatory standards while maximizing operational efficiency.
IT SUPPORT
Pharmaceutical SMEs face numerous challenges in today’s rapidly evolving regulatory and technological environment. The need for robust IT infrastructure and adoption of AI-driven technologies are critical. However, SMEs often lack the internal resources and budget to fully harness these advancements.
DATA COMPUTING
Unlock the power of data with EuroPharMedTech's computing solutions, transforming complex information into actionable insights for the pharmaceutical industry.
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TRAINING
Unlock unparalleled professional growth with EuroPharMedTech's eLearning: interactive, customizable modules and secure LMS, designed for the dynamic needs of the pharmaceutical industry.
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MEDICAL AFFAIRS
Empower healthcare professionals and engage patients with EuroPharMedTech's tailored medical affairs and communication solutions, bridging expertise with care.
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REGULATORY AFFAIRS
Our Regulatory Affairs services ensure seamless compliance with EU and global regulations, supporting pharmaceutical companies in obtaining approvals, maintaining product registrations, and navigating complex regulatory requirements efficiently.
PHARMACOVIGILANCE
Pharmacovigilance is critical for marketing authorization maintenance. It requires a thorough knowledge of EU regulations and local regulatory agency requirements.
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MEDICAL INFORMATION AND PUBLICITY
Enhance compliance and knowledge with EuroPharMedTech's expert regulatory medical writing and impactful scientific publications.
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MEDICAL REGULATORY AND TECHNICAL WRITING
Enhance compliance and knowledge with EuroPharMedTech's expert regulatory medical writing and impactful scientific publications.
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