Parenteral Drug Development
PARENTERAL DRUG FORMULATION, PROCESS DEVELOPMENT & FILL-FINISH
Injectable Drugs and Biologics
Pii enables biotech and pharmaceutical companies to accelerate timelines dramatically. Our proven capabilities include aseptic filling, terminal sterilization, lyophilization of biologic NCE, small molecule, potent (HPAPI) up to SafeBridge® Category 4, and cytotoxic drugs into vials, syringes, and cartridges.
Our focus is on accelerating decision-making at every step of the drug development process utilizing QbD to meet your project milestones, while also providing rapid access to manufacturing slots and quick release of drug product for clinical trial or commercial supply. All parenteral products are processed and tested in strict accordance with cGMP requirements. Our services include:
Sterile dosage forms
Lyophilized products
Suspensions and highly viscous liquids
Long-acting and depot injectables
Vials, syringes and cartridges
Drug device combination products
