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To better assist you with your request, please choose a research area provided by Life Science People. 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.
Health Economics and Outcomes Research (HEOR)

Evaluate data collected during drug development to maximize the value of a therapeutic product.
Market Access

Find general strategies and methods used to market a pharmaceutical product or device.
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.
Real-World Data

Acquire real-world data from patients' electronic medical records including clinical information generated during the course of healthcare.
Biostatistical Design

Use statistics to ensure appropriate pre-clinical and clinical study design.
Database Management Software

Facilitate the collection, tracking and processing of biological facts, statistics and observations.
Regulatory

Ensure that each product or device complies with all FDA rules and regulations.
Health Technology Assessment Submission (HTA Submission)

Analyze the medical, social, ethical, humanistic, and economic considerations of a drug, medical device, or clinical procedures. Submissions are sent to regulatory agencies with different requirements that govern submissions. See also AMCP and Value Dossier.
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