Facilities
Integrated Facilities Supporting End-to-End Development & Manufacturing
CPL operates 180,000 square feet of FDA‑ and Health Canada‑approved facilities in Mississauga, Ontario, purpose‑built to support the full lifecycle of semi‑solid and non‑sterile liquid drug products. Our Danbro site houses GMP manufacturing, packaging, warehousing, and product development laboratories. At the same time, our Meadowpine campus provides GMP-quality control, microbiology, skin testing, and ICH‑compliant stability capabilities, enabling integrated, compliant, and scalable pharmaceutical development and supply.
Our Facilities
Danbro
GMP Production Facility
The Danbro production facility is a 140,000‑square‑foot, FDA‑ and Health Canada‑registered site housing GMP manufacturing, packaging, and warehousing, complemented by a dedicated non‑GMP product development laboratory to support efficient scale‑up and commercialization.
Manufacturing
Supporting Technologies & Infrastructure
Packaging, Labeling, Serialization & Aggregation
Supporting Technologies & Infrastructure
Meadowpine
Analytical & Testing Laboratories
The Meadowpine laboratory is a 40,000‑square‑foot, FDA‑ and Health Canada‑registered facility providing GMP-quality control, microbiology, and Skin Lab skin testing, supported by ICH‑compliant stability chambers and long‑term stability testing services.
Analytical Method Development & Product Testing
Supporting Technologies & Infrastructure
Skin Lab – Skin Testing
Supporting Technologies & Infrastructure
Commitment.
Partnership. Legacy.
Leverage CPL’s 35 years of expertise in non-sterile liquids and semi-solids to ensure your program's success. We’ll support your product from molecule to market, or step in at any stage of its product lifecycle.