Public Profile

We perform a wide range of duties such as study start-up activities, ongoing study management, providing care and coordination of participants at every stage of their clinical trial journey, ensuring milestones and project work are met within agreed times framework. Communicates effectively with all staff referring doctors, colleagues, patients, sponsors and where necessary the public. To be more particular we help with recruitment and retention of patients, coordinate the day - to - day running of the trials, collect data, and produce reports, also we take responsibility for ensuring a trial's safety and keeping the materials used safe during the study, etc. We work with EDC (eCRF), IVRS (IWRS), Reading Centers (DARC, Excelsior,etc.), JUDI, VeevaVault, etc. We have experience with CROs like - SYNEOS, IQVIA, BAYER, PPD, ICON, ASTRA ZENECA, etc. We are GCP and IATA certified. We have certified lab assistant who can collect and process biological samples during patient visits. We are currently working with and have experience in cardiology, ophthalmology, urology, otorhinolaryngology, etc.