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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.
Regulatory

Ensure that each product or device complies with all FDA rules and regulations.
Health & Pharmacoeconomics

Identify, measure and compare the cost-benefit ratio of products and services.
Case Report Monitoring & Auditing

Ensure the adequate collection and traceability of clinical data in preparation for review by the FDA.
ePRO - Electronic Patient-reported Outcome

Patient reported outcome collected by electronic methods.
Nutritional Trials and Studies

Conduct clinical trials to test the efficacy and safety of food and dietary products.
IP Packaging

Proper packaging of pharmaceutical products and goods is crucial to ensure the validity and quality of the product being supplied. Proper investigational product packaging is aided by the use of quality assurance, and adherence to annex 9 guidelines as developed and produced by the Food and Drug Association.