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To better assist you with your request, please choose a research area provided by Gsap. 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.
Quality Control

Ensure products or services adhere to a set minimum standard.
Publication Writing

Make clear and accurate presentations of scientific and technical data.
Site Monitoring

Maintain oversight over participant's health during a clinical trial.
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.
Site Selection

Select clinical trial sites with clinicians who recruit, enroll, treat and evaluate trial patients.
Pharmacokinetic Studies

Design a study that observes the time course of drug absorption, distribution, metabolism, and excretion, as means to test the safety and effective therapeutic management of drugs in an individual patient.
Case Report Monitoring & Auditing

Ensure the adequate collection and traceability of clinical data in preparation for review by the FDA.
Investigator Recruitment

Enlist clinical research experts to assist in investigator selection, recruitment monitoring and database evaluation.
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