VI.REL Pharma provides the most comprehensive solutions for every stage in the lifecycle of your pharmaceutical products
Specialized consultancy that supports your products from the development phase all the way to the marketing phase, incorporating services in Pharmacovigilance, Regulatory Intelligence, and Medical Writing
PHARMACOVIGILANCE
VI.REL provides comprehensive pharmacovigilance system management and personalized services tailored to meet the unique needs of each client. Our extensive range of services is designed to ensure the safe and effective use of pharmaceutical products, from the clinical development phase through to the post-marketing stage
REGULATORY AFFAIRS
Our team of regulatory affairs experts is dedicated to ensuring that your company adheres to current rules and regulations, prioritizing the safety of your product at every stage
MEDICAL WRITING
VI.REL Medical Writing offers expert, specialized support across a broad spectrum of pharmaceutical services throughout all stages of a product's lifecycle, delivering our clients high-quality scientific documentation
CLINICAL TRIALS
Good Clinical Practice (GCP) stands as a global benchmark for ethical and scientific quality in designing, documenting, and reporting studies involving human subjects.
OUR COURSES
From our experience springs VI.REL MASTER CLASS, offering a wide range of in-person and online courses for individuals and companies, featuring the finest specialists in the field
WHO WE ARE?
We are an innovative team of international professionals with multifaceted expertise, seamlessly blending scientific, medical, and regulatory knowledge to offer specialized support to our clients in the SEE, USA, and Asian regions
25+ YEARS OF EXPERIENCE
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PARTNERSHIPS WITH GLOBAL CORPORATIONS
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70+ CLIENTS
DEVELOPMENT OF A WIDE RANGE OF PRODUCTS
200+ REGISTERED MAAs
