Services

Nutraceutical Medical Research provides a variety of clinical research, medical writing and consulting services including:

A. Basic Science and Clinical Research Services

Clinical trial development

• Protocol development for basic science and preclinical research, pilot studies*, and phase I-IV clinical trials
• Investigator brochures
• Case report forms, clinical site binders and study reports
• Institutional Review Board (IRB) submission and maintenance
• Statistical analysis

Clinical Site Selection and Management of Clinical Trials

• Site screening and site selection: screening of clinical sites and selecting the site that is needed for running your clinical trial. We have a wide variety of clinical sites and investigators in our database including academic centers, free standing research clinics and community hospitals. We also have an extensive pool of investigators with a variety of specialties including: allergy, dermatology, gastroenterology, gynecology, infectious disease, integrative medicine, internal medicine, oncology, pain management, urology and CAM specialties including acupuncture and traditional Chinese Medicine, homeopathy and naturopathy.
• Management of site throughout clinical trial period: Data and safety monitoring, site auditing and interim reporting to sponsors.
• Maintaining INDs and other FDA requirements for sponsors.

Data Management

• A capable and efficient management team that carefully manages your data.
• Timely data collection and robust analysis
• Database creation of your survey and other product/ingredient information
• Database storage

Clinical trial reporting

• Written summaries of clinical trials
• Clinical Reports/Case studies
• Manuscript preparation for academic journals
• Poster writing and layout, other reporting tools

B. Medical Writing

• Literature reviews on your product/ingredients
• White papers and technical reports
• Efficacy summaries for business and marketing strategies
• Safety summaries and risk/benefit papers
• Clinical application/use and guidelines for labeling

C. Consulting

Basic services provided in any of the following areas:

• Basic science investigations
• Clinical trial development
• Clinical writing
• FDA/FTC questions
• IND preparation and filing
• IRB protocol preparation and filing
• Label review
• Market research
• Medical food application preparation and filing
• Strategic planning
• Statistical analysis

* We offer an affordable, quick and powerful way to obtain preliminary human clinical efficacy data via our Rapid Focus Study™. Rapid Focus Studies can be done on new, developing or on-the-market ingredients or finished products such as cosmeceuticals, dietary/herbal supplements, functional foods or beverages or ingredient applications for which structure/function claims are made.

The Rapid Focus Study™ process

1. Review your product or ingredient with the NMR team


2. Discuss short/long-term goals and timeline


3. Tailor study parameters with NMR:


• Choose study length: from 1 day to 1 month


• Select metrics from NMR's Rapid Focus Study™ portfolio: qualitative, quantitative or clinical analyses (blood, urine, imaging, etc.)


4. Receive progress and data updates on your Rapid Focus Study™


5. Receive your Rapid Focus Study™ Report demonstrating your product's or ingredient's results


6. Disseminate your study results to investors, manufacturers, retailers and customers