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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