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To better assist you with your request, please choose a research area provided by dMed Biopharmaceuticals. In case you cannot find an exact match, simply select any service, and our concierge team will swiftly address it once your request has been submitted.

Clinical Trial Design

Develop study-related protocols, case report forms (CRFs) and database tools for records management.
Medical Writing and Editing

Communicate scientific, technical and health-related information to a range of audiences.
Quality Control

Ensure products or services adhere to a set minimum standard.
Bioequivalence Studies

Assess the expected biological equivalence of two proprietary preparations of a drug.
Publication Writing

Make clear and accurate presentations of scientific and technical data.
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 maintained as well as maintaining the integrity of the data collected during the trial.
Real World Evidence (RWE) Studies

Studies (prospective or retrospective) utilizing data obtained from "real world settings" , and is outside the tight controls of a clinical trial design.
Site Monitoring

Maintain oversight over participant's health during a clinical trial.
Biostatistical Design

Use statistics to ensure appropriate pre-clinical and clinical study design.
Regulatory

Ensure that each product or device complies with all FDA rules and regulations.
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