Dive into the evolution of EU Pharmaceutical Legislation

Join us as for an insightful webinar on MA procedures in light of the EU Pharmaceutical Legislation Reform

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Unlock the potential of pharmacovigilance

Handling volume and data explosion through our agile data processing and technology-driven solutions

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Quality defines our services

Quality is enshrined in our systems and processes to protect patients’ and public health

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Adaptable business models and operational excellence

Integrative project management that delivers quality safety services and connects you to the right solution

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A flexible partner for greater control in product safety

Dedicated resources seamlessly integrate into fast-pacing matrix environments and deliver under pressure

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Excellence in our deliverables

We strive for excellence in our global safety services through our trustworthy partnership with you

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Full Lifecycle of Pharmacovigilance Services

End-to-end services ranging from ICSR processing to benefit-risk management and from our extensive network of QPPVs & LCPPVs to inspection readiness.

Clinical Research and Development

Optimum clinical safety management of medicines and devices

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Regulatory Review and Registration

Management of the safety profile of medicines and devices peri-approval

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Post-marketing

GVP assurance and safety control across your product's lifetime

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Clinical Research and Development

Optimum clinical safety management of medicines and devices

Learn more

Regulatory Review and Registration

Management of the safety profile of medicines and devices peri-approval

Learn more

Post-marketing

GVP assurance and safety control across your product's lifetime

Learn more

Insights Hub

Access our trending topics and latest experts' articles, watch our hot topic webinars and read what you may be interested in learning.

Why PrimeVigilance?

We offer end-to-end PV services and solutions from clinical development to post-marketing. Our footprint, continuous investment in automated technology and resources, and product expertise render us the partner of choice.

k+

ICSRs/SAEs processed per year

m+

Literature abstracts reviewed annually

%

Employees with life science degrees

What our Partners say

Thank you for such amazing support – we could not have done this without you! Your team’s dedication, quick turnaround, subject matter expertise, and kindness are to be recognized! Thanks for your continued commitments to quality.

Clinical Quality Leader

Mid-size US biotech company developer of gene therapy treatment

It has been a pleasure working with you, having your expertise and prompt support with our literature search activities – all much-much appreciated!

Group Medical Director, Medical Safety Review Worldwide Patient Safety (WWPS)

Large worldwide Pharmaceutical company

I've been most impressed by your quarterly safety detection methods and would like to incorporate them for other studies I am responsible for.

Chief Medical Officer

Specialty Pharma

I wanted to write to you to let you know of the excellent help and support we received prior to and during the Inspection by members of the PrimeVigilance team.

Senior Quality Assurance Manager

Swiss Pharmaceutical Company

We sincerely thank you all for your help and successful labor during this year and we are looking forward to work with you as well in the future.

Head Safety Processes Manager

Global Drug Safety Section

Knowing I have you as partners helps me sleep soundly at night.

CMO and Director of Compliance

Pharmaceutical Company

Careers

Our success begins with our people. Build you career in clinical development at a company striving to improve the lives of patients around the world.

Find out how we help our partners

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