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To better assist you with your request, please choose a research area provided by Clinexel Life Sciences Private Limited. 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.

Medical Writing and Editing

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

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

Summarizes the results of research (that meet pre-defined eligibility criteria for inclusion) and provides a high level of evidence on the outcomes assessed.
Observational Research

Research method for documenting clinical, economic, and or humanistic outcomes of actual medical practice absent the constraints of a more formal experimental design. See also Pragmatic Clinical Trials.
Case Report Monitoring & Auditing

Ensure the adequate collection and traceability of clinical data in preparation for review by the FDA.
Study/Site Feasibility Study

Explore and test study practicality.
Registries - Patient

Database containing, through utilizing observational research methods, standardized data about patients who have the same condition, disease, or exposure and is used to evaluate an outcome
Registries - Disease

Database containing, through utilizing observational research methods, standardized data about patients who have the same disease.
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