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Safety

When it comes to patient safety, you want first time right.

Benefit from end-to-end safety solutions that span the product life cycle of drugs, medical devices, combination products, vaccines, cell and gene therapies, consumer goods and cosmetics—from early clinical phases through post-approval.

Proven compliance

We process over one million ICSRs annually, achieving ~99.5% regulatory compliance over the past 5 years, with a focus on first time right (FTR) execution.

High client satisfaction

Serving over 150 multinational clients, we maintain customer satisfaction ratings of 85%+, with clients rating Fortrea 9/10 or 10/10 for our reliable services.

Expertise and best practices

With over 3 decades of safety experience, our team of 2,700+ experienced safety professionals around the world delivers quality and regulatory compliance you can trust.

Expert guidance and proven experience

Our global team of pharmacovigilance experts meets your milestones in patient safety and post-marketing activities with a flexible team and scalable infrastructure. They expertly use industry-standard safety systems and proprietary automation to maximize efficiencies and address your country-specific needs. Plus, our innovation-driven systems and processes drive operational efficiencies across the continuum, while our extensive experience and metrics-focused teams deliver quality and regulatory compliance—all to deliver on our promise of an excellent customer experience.

Testimonial

It’s a privilege to be working with each one of you. Amazing team and amazing accomplishments!!! Simply put—Fortrea is an incredible team who has stepped up each time to deliver over and over again.

Director PV Automation

Fortrea is an incredible team who has stepped up each time.

Flexible patient safety solutions

We develop strategic partnerships, approaches and practices to gain efficiencies and increase the value of your operations. Partner with us and control your journey from start to finish:

  • Medical contact center
  • Case processing
  • Medical review
  • Aggregate reporting
  • Safety surveillance
  • Qualified Person Responsible for Pharmacovigilance support