About AMRs

All what you need to know about our company

AM Regulatory Solutions

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 MISSION

Our mission is to establish a chain of well equipped, quality and result oriented, clinical trial sites across Asia Pacific for execution of clinical trials in full compliance to international regulatory requirements

OUR VISION

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.

OUR CORE VALUES

  • Team work
  • Honesty
  • Hard work
  • Dedication
  • Discipline

Some of our key Solutions

Our Skills

Site Management
95%
Project Management
90%
Clinical Monitoring
85%
Regulatory Solutions
85%

We are technology and innovation driven

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.

• We have an exclusive agreement with large multi-specialty hospitals and medical colleges who are having a pool of highly experienced clinical practitioners of various domains/specialties.

• Each site team is comprised of experienced research coordinators, experienced clinical research investigators, experienced staff nurses, experienced pharmacists, and laboratory personnel.
• Site Managers, Network Managers, Directors, and an Executive staff ensure proper communication among our sites.

• Central QA/QC team for assurance of data quality and training of site team

• Comprehensive SOPs for each site/study activities

• Periodic calibration of site instruments

• Dedicated clinical refrigeration and freezer
• Comprehensive diagnostic testing (i.e., radiologic, imaging, Cath Labs and endoscopic procedures)

• IRB/IEC with full time site EC/IRB coordinator

• Fire proof cabinets for archival of study documents

• Dedicated access and temp/humidity-controlled pharmacy

Our Team

More About AMRs Team

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.