We offer Clinical Research Services comprising of Medical Writing, Clinical Data Management, Site Management, Biostatistical and Regulatory Services making us boutique CRO (Contract Research Organization) offering an end to end services with an international reach, combined with the level of quality and customer service.

As a client you will benefit:

• Working with a company that has the capabilities of a truly full service, International organization, with a breadth of service, capabilities and expertise not seen outside of the very largest CRO’s, but with a scale where you matter a proven provider offering quality and reliability.
• The company that is drawing best in the industry, Bio Pharma and CRO, to ensure we think and deliver like drug developers.
• A lean managerial infrastructure ensuring senior oversight and governance on all the programs we work on.
• A company with experience and expertise in working in some of the most complex areas of Clinical Research.
• Efficient, nimble and responsive customer care.
• Each Clinical Study assigned a seasoned Project Manager who is your main point of contact throughout the study and is responsible for driving the activities of the study team. Our Project Managers are supported by the most senior and experienced personnel within the company. This occurs informally on an ‘ad hoc’ day-to-day basis and in the most structured setting of monthly Project Review Meetings.
• Direct access to them and to all other members of your study team as required.
• It is important to ensure that regular communication is maintained throughout the entire duration of the project.
• Established trial management procedures and processes for rapid study start-up and efficient conduct of your study.
• Close cooperation with central labs, data management, IMP management, regulatory affairs etc., to drive your study and keep it on track.