Our consultants can engage investigators more likely to help you meet your patient enrolment goals from the start. We work very closely with clinical trial sites to ensure that they are adequately trained and fully understand the protocol and trial related procedures. Our CRA’s undergo extensive and regular training programs both for clinical trials as well as general clinical research knowledge.
Beyond recruitment, we help you optimize study cycle time, uncover supply chain needs and better manage your study budget. We have processes to ensure efficient, timely and accurate invoicing, which helps you stay within +/-5% of your planned budget more than 90% of the time. This mitigates the surprises that can impact your ROI.
Our management team has a cumulative health research delivery experience of over 50 years in UK, Europe, Middle East and Pakistan. Our management team has held key leadership positions and has worked with major pharmaceuticals, biotechnology, contract research organizations and world leading academic research centers. We have substantial knowledge and experience to support clients in the drug development industry with proven track record of successful clinical trials (phase II-IV) and post- approval studies.
We have extensive experience in Europe (UK and Major European countries) as well as Asia and Africa (Saudi Arabia, United Arab Emirates, Qatar, Oman, Kuwait, Bahrain, Syria, Jordan, Lebanon, Tunisia, Morocco, Algeria, Egypt and Pakistan).