HAt Aurous HealthCare, we pride ourselves on our extensive network of over 500+ doctors all over the Country. As a niche service or as part of our End to End Clinical Trial Service, we provide comprehensive coverage from study feasibility to close out.
Our Clinical Trial Associates and Monitors are trained and equipped to handle the conduct of study for any product ranging from Herbaceuticals, Nutraceuticals, Cosmeceuticals or Medical Devices. In a country like India, we are assured about our network comprising of leading experts in the field of Alternate Systems of Medicine – Ayurveds, Siddha, Unani that not only provide lateral perspective but also aid in development of your niche ASU product.
We are confident of our customizable Conduction Stage Project Planning and Management that will allow your product to be studied in the best of clinical sites across India.
Because our monitors are seasoned and headed by a Medical Director, they are able to engage in substantial discussion with potential investigators and understand their pulse and passion for the clinical study. This coupled with their extensive knowledge of the protocol requirements and local regulatory guidelines enables us to select and sign the finest and most devoted of Investigators of therapeutic expertise for your Clinical Study. Our team works from Study feasibility, selection of Investigators and Trial sites, training of site staff, periodic monitoring of the clinical study to study close out.
Our team is proficient in planning and implementation of patient retention programs, rescue services and emergency monitoring services for the clinical study of your product already in development. Our active and continuous communication lines with the investigator site not only allow for monitoring of the data capture but also ease the process of query resolution.
We supplement inadequately staffed clinical trial sites with our In house Coordinators who work for the Investigator and thus bridge any lapses in time, data or investigational product management because of staffing issues.
Our Site Management services are the most cost effective quality-driven solution for clean data from your clinical study. Our regulatory affairs teams also assist first time investigators with submissions to regulatory authorities. Our monitors are trained continuously to keep abreast of the latest regulations in the drug research sector. This guarantees that there are minimal to no deviations from the Clinical Study Protocol and that timelines are met with sincerity..