Welcome to

AM Regulatory Solutions

AM Regulatory Solutions (AMRs), a venture with multidimensional network of clinical trial sites across India. Under the umbrella AMRs a team of highly skilled professionals and a network of multispecialty hospitals and medical colleges are working for betterment of human health. Our goal is to make participation of new drug clinical trial feasible for both medical fraternity and patients in every corner of Asia pacific region.

About AMRs

OurServices
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SPONSOR / CRO

AMRs assists sponsors and CROs in conducting onsite and offsite feasibility and site selection.

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SITE / INVESTIGATOR

AMRs provides the site and the investigator with trained and qualified staff to assist and handle the projects.

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ETHICS COMMITTEE

AMRs provides necessary support to new ECs in preparing the documents as per the guidelines.

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BENEFITS of AMRs

Working with a AMRs can benefit Sponsor/CRO/Site in a number of ways

AMRs Best For Your Trial

To keep the pace and alignment with changing rules and regulations of the regulatory authorities we keep on updating and training our team and 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/Network Managers, Directors, and an Executive staff ensure proper communication among sites.
  • Central QA/QC team for assurance of data quality and training of site team.
  • Comprehensive SOPs for each site/study activities.
  • All sites have customized and dedicated monitoring workspaces.
  • 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.
  • Discipline

Some Facts

Monitor and measure performance as outlined in each custom plan.

Participants
Study Sites
Trials

Project Management

Clinical Monitoring

Data Management

Medical Writting

Site Management Organization

Site Startup (SSU)

Site Service

GCP Training