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Comparator Drug Sourcing

Streamline new drug development and clinical trials by comparing the efficacy of an experimental drug to a comparator drug.
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.
IP Shipments & Resupply

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.
IP Returns & Destruction

Return the used and unused IP to the clinical trial sponsor for destruction, as well as send the used and unused IP for destruction in accordance with institution policy, or the standard operational procedure. Theses SOPs are in correspondence with GMP protocols.
IP Storage

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.
IP Labeling

Proper IP labeling guidelines are produced by the Food and Drug Association. Based on the compound or product in need of proper labelling there are guidelines that can be followed.