Universal Clinical Research was established and privately held since 2017 is a Site Monitoring Organisation (SMO),Since then SMO-India has been providing exceptional site management and project management and monitoring of phase II, III and IV clinical trials involving pharmaceutical, biological and medical device products to its clients. We maintain High retention of our clients due to our commitment, responsiveness, flexibility, performance, cost effectiveness and unmatched quality. We complement each client’s working culture and management style and are flexible to their requirements.
Clinical trials are carried out under the strict supervision of fully qualified doctors, nurses and other health professionals and all trials must first be approved by an Independent Review Board (IRB). IRBs comprise both laypersons and professionals – their main concern is safeguarding the interests of the participants.
A universal clinical studies are done in accordance with ICH Clinical Practice (GCP) which is an international ethical and scientific quality standard for the conduct of trials. We also follow the regulatory guidelines set by the country that the study is being conducted in.