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To better assist you with your request, please choose a research area provided by Pharma Consulting Services (PCS) Inc.. 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.
General Toxicology

Use in vivo models to assess acute and sub-acute toxicity as well as chronic and sub-chronic toxicity.
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.
Site Monitoring

Maintain oversight over participant's health during a clinical trial.
Patient Recruitment

Recruit and retain patients for clinical trials.
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.
Small Molecule Drug Development Consulting

Request consulting services related to small molecule development.
Chemistry, Manufacturing and Controls (CMC) Consulting

Consultant services related to the development of pharmaceutical and biopharmaceutical drug products that are consistently effective, safe and high quality for consumers.
Large Molecule Drug Development Consulting

Develop large molecule drugs and complex biologics that have a therapeutic effect.
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