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.
VI.REL Master class corsi courses

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
VI.REL Team

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

CONTACT US

+39 011 0014838; mail@virelpharma.it