North Dallas Research Associates

North Dallas Research Associates

Research, 4201 Medical CTR Dr, McKinney, Texas, 75069, United States, 1-10 Employees

ndresearch.com

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Who is NORTH DALLAS RESEARCH ASSOCIATES

At North Dallas Research Associates, we are playing an active role in clinical research by conducting FDA approved pharmaceutical and device trials in a broad range of therapeutic areas f...

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  • 4201 Medical CTR Dr, McKinney, Texas, 75069, United States Headquarters: 4201 Medical CTR Dr, McKinney, Texas, 75069, United States
  • 2003 Date Founded: 2003
  • 1-10 Employees: 1-10
  • dollar-icon Revenue: $1 Million to $5 Million
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Research

SIC SIC Code: 8011 | NAICS Code: 621111 | Show More

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Frequently Asked Questions Regarding North Dallas Research Associates

Answer: North Dallas Research Associates's headquarters are located at 4201 Medical CTR Dr, McKinney, Texas, 75069, United States

Answer: North Dallas Research Associates's official website is https://ndresearch.com

Answer: North Dallas Research Associates's revenue is $1 Million to $5 Million

Answer: North Dallas Research Associates's SIC: 8011

Answer: North Dallas Research Associates's NAICS: 621111

Answer: North Dallas Research Associates has 1-10 employees

Answer: North Dallas Research Associates is in Research

Answer: North Dallas Research Associates contact info: Phone number: Website: https://ndresearch.com

Answer: At North Dallas Research Associates, we are playing an active role in clinical research by conducting FDA approved pharmaceutical and device trials in a broad range of therapeutic areas for many industry-leading pharmaceutical companies and clinical research organizations since 2003. North Dallas Research Associates is located 30 miles north of Dallas in the fast growing McKinney area, which is part of Collin County. We specialize in Phase II-IV outpatient clinical trial management. We also recruit clinical trials for physicians and other clinical research sites. We are knowledgeable, experienced, organized, efficient and very motivated. We utilize Central IRBs for rapid approvals. We understand importance of strict timelines. Routinely, we complete regulatory work and contract execution within 2 weeks of site acceptance and start screening our subject database before site initiation visit. We have met all enrollment targets and are frequently the leading enrollment site for multi-centered trials.

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