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Accell has launched new challenging projects

Accell's team is enthusiastic to announce that it is about to start two new Phase III studies in oncology and ophthalmology. The Sponsor of the studies has previously faced recruitment

European Union Clinical Trial Regulation 2023 update

The European Medicines Agency (EMA) has hit an important milestone in its clinical research regulations. Since January 31, 2023, under the Clinical Trials Regulation (CTR - Regulation (EU) No 536/2014),

Accell attended CPHI Frankfurt 2022

On November 1-3, 2022 Accell's Director of Clinical Operations in Europe, Daniela Pirvu, MD, attended CPHI Frankfurt which took place in Messe Frankfurt, Germany in-person for the first time since

Romania updates its regulatory legislation to align with the EU regulations

On July 20, 2022, Law 249/2022 entered into force stipulating a mandatory 60-day approval by the ANMDMR (National Agency for Medicines and Medical Devices in Romania) for a new clinical

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