When you absolutely have to recruit patients on time
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),
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
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
Accell Clinical Research is happy to announce that on July 4, 2022, the CRO has expanded its presence in the European Union by opening a new office in Bucharest, Romania.