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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 NDA's, ANDA's, 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.
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 […]
Released By CPL
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.
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