Silver Sponsors
Billev Pharma East
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Billev Pharma East is a regulatory affairs consultancy for human and veterinary medicines and medical devices, supporting EU submissions, strategy and lifecycle management, with strong expertise in electronic Product Information (ePI) Implementation.
Biomapas
Biomapas is a premier contract research organisation (CRO), delivering flexible solutions throughout the lifecycle of your product, as a seamless extension of your team. Our colleagues, spreading across all European, Commonwealth of Independent States (CIS), Eurasian Economic Union (EAEU) and Middle East/North Africa (MENA) regions, can enhance your drug development, accelerate your path to market authorisation, and ensure compliance with local and global post-marketing requirements. We do so through a complete service scope in Regulatory Affairs, Clinical Research, Pharmacovigilance, and Medical Information.
Clarivate
Clarivate is a leading global provider of transformative intelligence. We offer enriched data, insights & analytics, workflow solutions and expert services in the areas of Academia & Government, Intellectual Property and Life Sciences & Healthcare. Our connected data, deep expertise and intelligence platforms empower life sciences and healthcare companies to deliver safe, effective and commercially successful treatments to patients faster. Clarivate is home to Cortellis, solutions for real world data, medtech, market access and commercialization and deep consulting expertise.
cormeo
cormeo unites the expertise of Docuvera, EXTEDO, Rote Liste, and medicines.ie to provide a seamless end-to-end approach to creating, managing, and distributing regulated information in the life sciences sector. Together, we build the trusted bridge between industry, authorities, healthcare professionals, and patients.
3D PharmXchange
3D-PharmXchange is a Netherlands-based consultancy supporting academia, biotech and pharma throughout the drug development lifecycle, offering strategic and hands-on expertise in regulatory affairs, CMC, non-clinical, clinical, and quality compliance.
Granzer Regulatory Consulting & Services
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Granzer Regulatory Consulting & Services offers support in all phases of drug and device development. From defining the right development strategy to submitting a marketing authorisation application, all the way through to approval and beyond, as a one-stop-shop for our clients.
SciLife
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Scilife is a validated eQMS built for life sciences companies. It centralizes quality processes—from document control to CAPAs, training, audits, and risk management—helping teams stay compliant, audit-ready, and focused on continuous improvement.