Advanced Medical Research Institute

Advanced Medical Research Institute

Research, 8780 Sw 8th St, Miami, Florida, 33174, United States, 1-10 Employees

amriresearch.com

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Who is ADVANCED MEDICAL RESEARCH INSTITUTE

Advanced Medical Research Institute, LLC was created to evaluate the effectiveness and safety of medications or medical devices as well as present an avenue for our participants to receiv...

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  • 8780 Sw 8th St, Miami, Florida, 33174, United States Headquarters: 8780 Sw 8th St, Miami, Florida, 33174, United States
  • 1-10 Employees: 1-10
  • dollar-icon Revenue: Under $1 Million

industries-icon Industry: Research

SIC SIC Code: 8011

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Advanced Medical Research Institute Org Chart and Mapping

Employees

Carlos Pelayo

Clinical Research Coordinator

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Frequently Asked Questions Regarding Advanced Medical Research Institute

Answer: Advanced Medical Research Institute's headquarters are located at 8780 Sw 8th St, Miami, Florida, 33174, United States

Answer: Advanced Medical Research Institute's official website is https://amriresearch.com

Answer: Advanced Medical Research Institute's revenue is Under $1 Million

Answer: Advanced Medical Research Institute's SIC: 8011

Answer: Advanced Medical Research Institute has 1-10 employees

Answer: Advanced Medical Research Institute is in Research

Answer: Advanced Medical Research Institute contact info: Phone number: Website: https://amriresearch.com

Answer: Advanced Medical Research Institute, LLC was created to evaluate the effectiveness and safety of medications or medical devices as well as present an avenue for our participants to receive promising new therapies that would not otherwise be available. We pride ourselves in making the health of our patients our top priority. Advanced Medical Research Institute is a general practice dedicated to serving those in the South Florida community. We are dedicated to delivering quality data and protecting the rights, safety, and well being of those who volunteer to participate in our studies. Our research staff receives extensive training to coordinate clinical trials and ongoing Good Clinical Practice/ ICH training. Prior to the start of any trial we perform a protocol feasibility assessment with the objective of producing the highest quality data with efficiency. This involves reviewing the protocol, subject recruitment, source documents, and our SOPs to assess potential barriers or issues and develop solutions. Our innovative approach offers faster recruitment of subjects, high retention, high data quality, and reduced training and monitoring costs.

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