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Research supplier
FDAMap
FDAMap is listed as a small business research supplier in the Scientist.com network, with 2 sites in 1 country.
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Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Small business
Clinical Consulting
- Clinical Protocol Design & Development Creation of clinical protocol document which details how a clinical trial is designed, relating to to the methodology, hypothesis, and operation of clinical trial to ensure the safety of the patients is...
- Clinical Trial Recruitment Recruitment, enrollment and retention of patients for clinical trials.
- Regulatory Consulting Ensure that each product or device complies with all FDA rules and regulations.
- Support Staff Recruitment Recruit nurses, clinical staff, certified clinical research coordinators and research support staff.
Clinical Trials
- Clinical Research Services Determine the safety and effectiveness of medications and medical devices.
- Clinical Trial Design Develop study-related protocols, case report forms (CRFs) and database tools for records management.
- Investigator Recruitment Enlist clinical research experts to assist in investigator selection, recruitment monitoring and database evaluation.
- Patient Recruitment Recruit and retain patients for clinical trials.
- Site Monitoring Maintain oversight over participant's health during a clinical trial.
- Site Selection Select clinical trial sites with clinicians who recruit, enroll, treat and evaluate trial patients.
Medical Communications
- Medical Publications Make clear and accurate presentations of scientific and technical data.
- Medical Writing and Editing/Manuscript Development Communicate scientific, technical and health-related information to a range of audiences.
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Pharmacovigilance
- GxP Compliance Monitoring Ensure products or services adhere to a set minimum standard.
Real World Evidence & Data
- Real-World Data Acquire real-world data from patients' electronic medical records including clinical information generated during the course of healthcare.
- Real-World Evidence Acquire clinical data from patients' medical records to analyze trends and the frequency of occurrence of different medical conditions.
Where it operates
Sites by country, with the cities in each.
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United States 2 sites
About this supplier
In the supplier's own words, as listed in the Scientist.com network.
Quality assurance and Regulatory affairs support services for pharma, biologic and medical devices companies. We provide the following services: FDA submissions, FDA meetings, FDA submissions (IND, NDA, BLA, PMA, 510k, IDE, Orphan drug, etc), Contract QA services, SOPs, audits, and training.
- Website
- www.FDAMap.com
Work with FDAMap on Scientist.com
For prices, more details, or to contact FDAMap, visit Scientist.com.
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