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7600 Danbro Crescent , Mississauga, ON, L5N6L6, CA
For more than 34 years, CPL has been a leading contract development and manufacturing organization (CDMO) by providing product development and commercial manufacturing services for non-sterile liquid, nasal, and topical pharmaceutical products to the global pharmaceutical industry. Our development, manufacturing and testing facilities are registered and audited with the FDA and Health Canada and have a solid record of regulatory compliance. Our product experience includes NDAs, ANDAs, 505b2, and regulated OTC products, and we provide formulation services to clinical trial materials through commercial product manufacturing. CPL's new filling and manufacturing technologies include Symex mixing vessels and new IWK tube and bottle filling capabilities supporting batch sizes from 50kg up to 5000kg. From product development to commercial production, CPL provides these solutions to our customers all under one location.
A Breakthrough in Liposome-Integrated Formulations
Released By CPL
This webinar will cover the intricacies of liposomal topical semi-solid products, focusing on their role in enhancing drug delivery through the skin. It will begin with an overview of semi-solid dosage forms, explaining their complex two-phase structure and how liposomes integrate into these formulations. Key topics will include skin anatomy, drug penetration pathways, and how […]
A Q&A with Lucy Zhao, manager of the Skin Lab at CPL discusses the importance of in-vitro Release Testing and how it supports topical drug development.
As drug modalities grow more complex, low bioburden powders for reconstitution are emerging as a critical strategy to ensure sterility, stability, and scalability.
Released By Upperton
Enhances its ability to serve regulated European markets while adhering to globally benchmarked quality and compliance standards.
By: Charlie Sternberg
From new supply chain dynamics to emerging technologies and shifting regulatory standards— learn how CDMOs are adapting to the new API manufacturing playbook.
Overcoming heightened development challenges.
By: Anshul Gupte
On February 10, USP experts take a deep dive into standards and solutions that support quality and performance across the drug lifecycle
Released By U.S. Pharmacopeia (USP)
CHOMax’s approximate 10-month timeline is based on suitable, standard IgG monoclonal antibodies.
By: Patrick Lavery
Medra’s Physical AI autonomously runs experiments end-to-end, interfacing with standard laboratory tools and instruments.
Underscores the facility’s dedication to upholding the highest standards of quality across operations.
The strategic move will enable Crown Bioscience to operate as a standalone entity under Adicon's ownership.
Will explore a potential collaboration focused on accelerating the development and future availability of a new treatment for Post-Traumatic Stress Disorder.
Save your seat for Contract Pharma's December 9th webinar with USP.
The certification highlights the company’s adherence to rigorous safety and traceability protocols within the cell and gene therapy supply chain.
Aims to deliver practical standards that make life sciences data AI-ready and interoperable from the lab through to manufacturing.
Senior Director of Business Development shares insight on industry trends and outsourcing.
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