Cody Laboratories is organized into several key departments, each one with a critical role in the production of our pharmaceutical products. The departments are:

  • Manufacturing: Responsible for physical production of pharmaceutical and resulting product.
  • Process Development: Responsible for overseeing the processes required to produce a new product, including the involvement of appropriate government agencies.
  • Quality Control Department: Responsible for the implementation of quality control procedures in the manufacturing process.
  • Quality Assurance Department: Ensures that the products manufactured consistently meet or exceed government regulations and customer requirements.
  • Quality Control Laboratory: Ensures that every product produced meets the highest standard of purity.
  • DEA: Regulates the activities to guarantee conformity which meets or exceeds governmental regulations regarding the manufacturing processes of the pharmaceutical industry.


Cody Laboratories, Inc. has been inspected by the FDA, DEA, DEQ, the Wyoming State Board of Pharmacy and customer auditors.

  • Any firm considering doing business with Cody Laboratories should know that we are fully committed to compliance with each one of these agencies.

controlled substance Registrations

  • Cody Laboratories, Inc. is registered with the DEA for Schedules I - V.








601 Yellowstone Avenue, Cody, Wyoming, 82414  307.587.7099   Corporate Governance