Cody Laboratories, Inc. (Cody Labs), a wholly owned subsidiary of Lannett Company, Inc., produces active pharmaceutical ingredients (API's) & finished dosage forms of pain relief medication. We're organized into several key departments. The departments are:
Manufacturing - Responsible for physical production of finished pharmaceutical products & active ingredients (API's).
Project Management - Responsible for the overall project plan & execution of new product development. Coordinates all departments in the development, scale-up, validation, & production of new API's & modifications to existing products & systems.
Process Development - Responsible for overseeing the processes required to produce a new product.
Validation - Responsible for the installation, operation, & performance qualifications of new equipment & processes as dictated by the FDA to ensure reproducible production.
Quality Control Department - Responsible for the implementation of quality control procedures in the manufacturing process, and the development of test methods to meet these parameters. Also responsible for overseeing product stability.
Quality Assurance Department - Ensures that the products manufactured consistently meet or exceed government regulations & customer requirements.
Quality Control Laboratory - Ensures that every product produced meets the highest standard of purity, as well as testing raw materials & intermediates.
DEA - Ensures that raw material procurement, development of new products & manufacturing are done in compliance with DEA Regulations.
- We are dedicated to providing the HIGHEST QUALITY generic bulk active pharmaceutical ingredients under cGMP conditions.