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To better assist you with your request, please choose a research area provided by Valentis Clinical Consulting Ltd. 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 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.
Phase 1-3 Studies

Design phase 1-3 studies that seek to identify if a drug is safe, effective, and more efficient than other available treatments on the market.
Data Visualization

Visualize data collected from clinical trials and/or clinical research.
Protocol and Study Reports

Write protocol and study reports, specifically relating to the drafting, writing, and editing of Clinical Safety Reports.
Case Reviews

Review medical cases from Clinical Trials.
Patient Narratives

Draft, edit and submit patient narratives to specific regulatory bodies such as the FDA. These patient narratives contain specific events experienced by patients during the course of a clinical trial.