Our SMO has top multispecialty hospitals and reputable medical colleges as part of its network of clinical locations. Each facility has all the necessary infrastructure and resources to conduct clinical trials in complete conformity with national and global standards and laws. Each AMRs site has a specialised, highly trained workforce, which makes patient recruitment and data collection simple and efficient. The advantage of having locally trained site personnel makes participation of trail participants simple as they feel comfortable with local employees to get all their questions and concerns handled in their preferred language. The safety of the participants is always prioritised and guaranteed by all site workers, who are well trained.
Our vision is to be a leading SMO (site management organization) for reputed medical colleges and multispecialty hospitals to make new drug trial participation feasible to both patients and medical fraternity.
We do in-depth research and assess the viability of potential sites to determine which ones are the greatest matches for your project. After the sites have been selected, we efficiently conduct the study start up activities.
.Phase I through Phase IV studies in the most important therapeutic areas are fully supported by our entire project management services. Our staff has developed its abilities and practical experience in managing drug studies.
The AMRs team works to bridge the gap between the sites and the sponsor, speed up patient recruitment, and manage the trial efficiently from beginning to end, ensuring a seamless transition through each stage of the clinical study.
To keep the pace and alignment with market demand we keep on updating our team, tools and systems with current available information technology gadgets and software/systems to meet expectations of our Participants, our Investigators, our Sponsors and our CRO partners.
AMRs is a team of highly skilled, motivated, quality conscious, experts (in their domains) and work for quality health care for humans. Our leadership, staff and investigators are masters in their respective domains (of drug developments) and possess adequate knowledge and experience to oversight and assure subject safety, quality data collection, regulatory compliance, and utilizations of information technology for smooth execution of trial related activities. All our team members are well versed with their role and always follow safety of participant as first priority.