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 NICR recognizes trends in managed healthcare and consequent limited revenues. An ideal option exists for physicians to engage in pharmaceutical, device and biotech clinical research trials appropriate for your practice through which to achieve additional revenue, provide patients with emerging, efficacious therapies and maintain an important channel to medical infomatics within your clinical category.
NICR provides physicians opportunity to start their first study, expand current trial operations and/or further develop their clinical research business through acquisition, partnering & merger.
Our professional, multi-lingual staff provides
the following services:
- Protocol Procurement & Review
- Budget Negotiation & Feasibility Planning
- Local and Central IRB Approval Processes
- Document Management
- Study Initiation
- Screening/Enrollment
- Clinical Research Case Report Form Management
- Data/QA Management
- Study Communication
- Site Close-Out
- Coordination of FDA/Sponsor Audits
NICR also provides Clinical Research Professionals that can manage each study patient in your office(s) per trial, helping you achieve significant savings rather than hiring full-time, dedicated research personnel for short-term projects.
Let NICR help you join the elite of medicine partnering with the exciting biotechnology industry becoming an active participant, with your patients, and staff; contributing to the advancement of medical science and unique, emerging therapies. The experience is both educationally and financially rewarding.
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