Select a relevant service

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.

Digital version of a patient's medical or health chart containing demographic, clinical, medical, and other treatment information.

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

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

This digital research platform allows researchers to monitor their clinical trials remotely.

Complex document that entails the entire clinical research strategy of a drug, describing the clinical studies that will be carried out for a pharmaceutical entity.

IP shipments and resupply aid in the management of shipping of clinical trial material from warehouses to clinical sites, or vice versa. Shipping and resupply aids in restocking, drug orders, shipment tracking, transit, or returns to reduce study drug waste and ensure total management over the shipment of drugs or clinical trial related materials.

IVRS and Drug supply services allow research conducting clinical trials to receive real time subject updates, drug supply and shipment tracking, and randomization for the clinical trial. These services allow for more controlled specification when conducting a clinical trial.

IP storage protocols are specifically defined by the U.S. Pharmacopeia, Japanese Pharmacopeia, and the European Pharmacopeia that specifically define the proper storage and transportation conditions of the pharmaceutical products to ensure the validity and the purity of the product being stored or transported.