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We are a full-service pharmacovigilance CRO, covering all areas of drug safety activities. With our offices based in the EU, North America, as well as low-cost countries, we can provide the full range of legally required drug safety tasks while meeting the requirements of any budget.
Starting Oct 20, 2023, the EMA will publish full RMPs instead of summaries. Join us for a live online training on both the current pharmaceutical risk management legislation in the EU and its upcoming changes! Regular fee 489 EUR per person, early bird fee 389 EUR until October 31st! Discounts available for additional attendees from the same company
We cover the full, global range of pharmacovigilance tasks for our clients while meeting the requirements of any budget. Find out more below:
We have been supporting our clients since 2017 in the global tasks of PV, with our CEO having more than 20 years of experience in the field. Find out more below: