Integrated Process

Our flexibility makes the difference.

AMR coordinates multi-site studies through integrated processes that maximize economies of scale and provide consistency. This results in shortened timelines and savings to clients. Integrated processes also allow Sponsors/CROs to engage multiple AMR sites in studies requiring multiple sites and diverse populations. Centralized, no-cost coordination includes, but is not limited to, single-point-of-contact communications/information dissemination as well as standardization of budget, contracts, and study source documentation.

Cross-site studies are able to:

  • Facilitate streamlined communications with the Sponsor and CRO
  • Draw from historical and current experience to maximize efficiencies and minimize timeframes of each study
  • Ensure centralized problem-solving to address issues impacting any study
  • Marshal the combined knowledge and expertise of AMR members
  • Simplify study monitoring by providing standardized source documents
  • Implement scheduled meetings and teleconferences to confer on specific study details, as needed
  • Offer standardized budget, contracts and centralized payments with timely regulatory document submissions
  • Access to CTMS Enterprise system utilizing a CRO / Sponsor portal providing up-to-date information regarding study status and enrollment specifics
  • Provide gratis expanded feasibility assessments and study design/protocol development consults
  • Require post-study debriefings to document “lessons learned”
  • Identify opportunities to involve all AMR Centers of Excellence as readily available resources

Our Processes

INTEGRATED 4 AMR's single point of contact coordinates standardized: + Budget + Contract + Source Doc Creation + Recruitment Plan + Central Payments for all AMR sites 3 Sponsor / CRO selects sites 2 AMR HQ coordinates CDAs & site feasibility assessments for all sites 1 Sponsor / CRO contacts AMR HQ about a new study
DIRECT-TO-SITE 4 Sponsor / CRO works with each site directly for: + Budget + Contract + Source Doc Creation + Recruitment Plan + Individual Site Payments 3 Sponsor / CRO selects sites 2 Each site contacted completes a CDA & the feasibility assessments and returns them to Sponsor / CRO 1 Sponsor / CRO contacts each site directly about a new study Site 1 Site 2 Site 3 Site 4 Site 5 Site 1 Site 2 Site 3 Site 4 Site 5 Site 1 Site 2 Site 3 Site 4 Site 5 Site 1 Site 2 Site 3 Site 4 Site 5