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To better assist you with your request, please choose a research area provided by Sitilop. 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.
Clinical Research

Determine the safety and effectiveness of medications and medical devices.
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.
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.
Patient Recruitment

Recruit and retain patients for clinical trials.
Clinical Outcome Assessments (Non-Patient Reported)

Measure a patient's symptoms, mental state and level of disease condition-related impact on daily life.
Clinical Trial Recruitment

Recruitment, enrollment and retention of patients for clinical trials.
Regulatory Affairs Consulting

Receive assistance ensuring compliance with regulatory requirements.
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