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Research supplier
ProtoMed BioSciences
ProtoMed BioSciences is listed as a mid sized 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: Mid sized business
Clinical Consulting
- Regulatory Consulting Ensure that each product or device complies with all FDA rules and regulations.
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.
Data Science/Bioinformatics
- Biostatistical Design Use statistics to ensure appropriate pre-clinical and clinical study design.
Medical Communications
- Medical Writing and Editing/Manuscript Development Communicate scientific, technical and health-related information to a range of audiences.
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.
ProtoMed BioSciences, Inc. provides comprehensive clinical data management, biostatistical, programming, medical monitoring, and medical writing support for the bioparmaceutical and healthcare industries. ProtoMed's team of physicians, scientists, and medical writers combine critical-thinking, clinical, and analytical skills with the ability to design studies, monitor trials, and clearly communicate complex medical and scientific topics. ProtoMed offers comprehensive study design, trial monitoring, data management, and regulatory documentation (phase 1 through 3), including medical writing...
Show the full description
ProtoMed BioSciences, Inc. provides comprehensive clinical data management, biostatistical, programming, medical monitoring, and medical writing support for the bioparmaceutical and healthcare industries.
ProtoMed's team of physicians, scientists, and medical writers combine critical-thinking, clinical, and analytical skills with the ability to design studies, monitor trials, and clearly communicate complex medical and scientific topics.
ProtoMed offers comprehensive study design, trial monitoring, data management, and regulatory documentation (phase 1 through 3), including medical writing of INDs/NDAs, electronic common technical documents (eCTD), as well as investigator brochures, clinical protocols, and clinical study reports.With a passion for excellence, our clinical research professionals consistently provide the finest medical research and writing services available.
ProtoMed has extensive experience with medical writing of clinical trial protocols and study reports according to FDA, ICH, and GCP regulations and standards. All medical writing of clinical study reports is in accordance with CONSORT (Consolidated Standards of Reporting Trials) guidelines.
- Professional associations
- BIOCOM, BioNJ
- Website
- www.protomed.org
Work with ProtoMed BioSciences on Scientist.com
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