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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.
Approved as the first targeted medicine in the EU in over a decade for chronic spontaneous urticaria.
By: Charlie Sternberg
Plans an expansion of its flagship biologics manufacturing facility in Frederick and construction of a new facility in Gaithersburg.
Sentry’s foreign trade zone expertise helps pharmaceutical companies mitigate risks from tariffs and global trade volatility.
Released By Sentry BioPharma Services, Inc.
AGC Biologics to provide GMP manufacturing for AAVantgarde’s two novel candidates designed to address progressive and irreversible vision loss.
Underscores the facility’s dedication to upholding the highest standards of quality across operations.
Enables efficient nucleic acid purification, helping researchers to move faster from sample to PCR testing.
Iglesias will lead global medical affairs for botensilimab (BOT) and balstilimab (BAL).
The strategic move will enable Crown Bioscience to operate as a standalone entity under Adicon's ownership.
Lessons Learned and Best Practices from a CDMO Perspective
Released By Upperton
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 the December 2nd webinar from Contract Pharma and Samsung Biologics.
Released By Samsung Biologics
Collaboration combines ATCC’s portfolio of authenticated cell lines with acCELLerate’s expertise in cryopreservation and its capabilities for large scale cell banking.
Enhances its ability to deliver modular cleanroom projects with greater speed, precision, and local support.
By: Kristin Brooks
Mahmood offers 25 years of experience as a biotechnology entrepreneur.
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