The Alliance for Multispecialty Research, LLC is a nationwide company of 17 Clinical Research locations recognized as among the most experienced in the industry. AMR acknowledges the importance of multi-site coordination using our standardized processes. This allows us to maximize economies of scale and consistency in order to exceed Sponsor goals ahead of schedule and under budget.
Learn About AMR
The Alliance for Multispecialty Research, LLC (“AMR”) performs clinical research trials to support pharmaceutical companies in developing new drugs. Founded in 1994, the Alliance for Multispecialty Research served as the hub for an alliance of high-quality research centers that wished to share marketing, business development and best practices for clinical research. AMR staff provided business development and marketing for the alliance members, and in certain cases provided central budgeting and contracting for studies that used the majority of the AMR sites. Most of the sites adopted the same or complimentary Standard Operating Procedures (SOPs), trial management software, and best practices for research, and collaborated on multi-site projects. In 2016, 9 of the members, representing 17 centers, agreed to merge their businesses into a single limited-liability company. Two additional centers ( Medisphere Medical Research Center and Heartland Medical, PC ) elected to remain legally independent, but agreed to align operations, continue to share marketing and business development, and work cooperatively with AMR. The affiliate sites bring value to AMR due to their strong reputation and experience within the industry (over 44 years cumulative), a hospital network of physicians adding greater than 72,000 potential subjects to the recruitment database pool, and additional team members involved with the integration business development force.
AMR differentiates itself from its competitors with:
- Dedicated research locations
- The ability for clients to contract with a single entity, and rely on that entity to train, recruit, and collect & report data
- Specialization, expertise, systems, and reproducible scientific results
- Larger volunteer database
- Better quality data than typical sites
- Extensive list of Investigators and specialists who actively participate in study recruitment, enrollment and study procedures
- Standardized study budget and contracts
- Ability to use either local or central IRB’s
- Remote data entry (RDE) capabilities
- Formal HIPAA compliance programs
- GCP training and investigator certification
- Applicable industry certifications and licensures
- Broad therapeutic range in research experience
- Quality management plan with dedicated staff ensuring the highest level of quality data for our Sponsors and CROs
The staff was very friendly. I’m satisfied with the program.