Clinical Monitoring and Project Management

Cropha is a Contract Research Organization (CRO) that has core business focus on clinical monitoring and project management. At Cropha we supply other CROs and pharmaceutical firms practical services and trial development assistance in their clinical trial work. Our services help our clients to achieve their business targets faster and more cost effectively.

Through our vast experience in clinical monitoring and project management we have the knowledge to help customers with the full or partial organisational, development and management of clinical trial projects.

We can provide these services in Belgium or the country of your choice. The trials can be coordinated at a single site or several in accordance to the project requirements and on the location of key participating physicians.

Our clinical documentation services comprise of translation, writing and review of clinical documentation. This service includes patient information & consent form, protocol, patient diary, etc.

At Cropha we recognise that clinical research is not always a consistent or constant factor for our customer CROs and pharmaceutical companies. We also recognise that projects differ in terms of size and resource requirements. To enable our customers to run clinical trials efficiently without increasing the number of staff, Cropha provides temporary CRA resources at competitive rates for as long as required.

For more information or to discuss Clinical Monitoring and Project Management please contact us directly.