TRIAL MANAGEMENT

Experienced management of Global Clinical Trials as well as consulting and ongoing support are available for Development and Planning and throughout the life of the study.

Our staff can generate customized study documents, handle the collection, tracking and storage of essential regulatory documents and create all the necessary study materias.

Our Clinical Associates are well versed and familiar with ICH (International Conference on Harmonisation) and with the proper GXP training and experience [GCP (Good Clinical Practice), GLP (Good Laboratory Practice) or cGMP (Current Good Manufacturing Practice)].

ESSENTIAL DOCUMENTS

Management of trial documents can be handled by PRC. Regulatory documents can be collected, filed and stored and even uploaded for online access to files.

TEAM WORK

Take advantage of our Project Management or have direct oversight with our regional staff and we'll ensure a communication plan that is right for you.

We work within our client's team to make sure they have the services they want-when they need them.

Our clinical team members can be managed jointly by PRC and the client. We have a customizable communication plan to keep our team in touch and up to date on each study.

SITE RECRUITMENT & MANAGEMENT

Finding study centers to participate is easy. Finding the most appropriate sites isn't. The best sites and locations for the conduct of a clinical trial depend on many factors. Location and clincal setting must come together with experience, site resources and adequate patient populations.

We can help match the required resources to identify sites and get them up and running as quickly as possible.