Celerion Protocols for Safe Clinical Research. Learn More


Continuous assessment of patient safety

Flexible 24/7 Pharmacovigilance Services

Celerion offers turnkey pharmacovigilance services to monitor, assess and report on the safety of investigational products and detect any change to their risk-benefit profile. We work closely with sponsors, sites and regulators to assure compliance against all relevant reporting requirements.

Celerion provides flexible solutions tailored to meet the needs of your project or program. Our systems and processes have been specifically designed to meet the needs of the full gamut of sponsors from two-men-and-a-molecule to even the most sophisticated organizations. Our comprehensive solutions provides a 24/7/365 global solution with local knowledge, assuring that safety and compliance remain a top priority.

Our services include:

  • Individual Case Study Report (ICSR)
  • Signal detection
  • Periodic reporting
  • Risk-benefit assessment
  • Medical monitoring

Full Service Global Clinical Development

Celerion, a full-service, early clinical CRO, is the leader in accelerating development for Phase I-IIb. Our unique combination of medical expertise, clinical operations experience and scientific excellence, enables you to make timely decisions with expert advice and high-quality data. Our leadership in clinical pharmacology through Proof-of-Concept is focused on helping you translate your science to medicine.

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Translating Your Science to Medicine.

Partner with us to get fast, actionable data you can rely on.

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