Study StartUp

We recognise that achieving site activation in the shortest time frame possible is a priority. That’s why all Accelagen clients are assigned a dedicated and highly-experienced Project Manager to support the startup process and oversee every element required to reach this major milestone. Your Project Manager can negotiate budget and site contracts with site personnel on your behalf before preparing and implementing a robust electronic Trial Master File (eTMF) to ensure regulatory compliance from the word ‘go’. Located within a comprehensive logistics framework that securely stores and distributes the Investigational Product to each trial site on time, our team is ready to support you to get everything you need prepared and approved en route to a successful clinical trial.