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AMCR Institute, Inc.

Improving lives through quality clinical research in diabetes and obesity

AMCR Institute, Inc.

AMCR Institute is an independent clinical research center engaged in Phase I-IV trials diabetes and obesity with a strong proprietary pediatric and adult volunteer database ensuring a fast, reliable and timely enrollment.
In addition to bio-pharmaceutical research, AMCR Institute carries out medical device trials from feasibility to pivotal. AMCR Institute tests both stand-alone and embedded software and can help with the software development process.
AMCR Institute understands human factors testing and aids with the requirements gathering process by facilitating focus groups of appropriate subjects.
AMCR Institute is well known and repeatedly contracted for glucose clamps with highly-customizable protocols for glucose manipulations (euglycemic, hypoglycemic and hyperglycemic clamps), delivering on conclusive data for clients and a better experience for study participants. We hold ourselves up to the highest standards by investing in highly qualified and experienced investigators and research staff.

Information

Demographic Data

  • SITE INFORMATION 
  • Start year clinical research2007
  • Phases of clinical studiesPhase I, Phase II, Phase III, Phase IV
  • Types of studiesBiologics, Drugs, Medical Devices, Nutraceuticals, Vaccines
  • PopulationsChild 2-10 yrs, Adolescent 11-17 yrs, Adult 18-64 yrs, Senior 65 yrs and over
  • SPECIFIC SITE INFORMATION 
  • Type of siteFreestanding
  • # of employees involved in research50
  • # of investigators1 PI; 5 Sub-I
  • Number of studies last year20
  • Days openMonday, Tuesday, Wednesday, Thursday, Friday
  • Extended office hoursYes
  • Overnight facilitiesYes
  • Dry iceYes
  • Blinded pharmacistYes
  • Dedicated monitoring spaceYes
  • Internet access for the monitorYes
  • Onsite laboratoryYes
  • Central laboratoryYes
  • Infusion capabilityYes
  • Shipping optionsFedEx, UPS, DHL, Other
  • REGULATORY INFORMATION 
  • Contact for regulatory documentsLaura Bedolla
  • Regulatory phone number7604661523
  • # of days to turn around regulatory documents5-7 business days
  • Type of IRB used by this siteCentral
  • Appropriate storage facilities for productYes
  • Able to appropriately store Schedule II drugsYes
  • FINANCIAL INFORMATION 
  • # days to turn around budget and contract10 business days