Safe handling of highly potent molecules is complex, and the associated regulatory requirements are growing. As a result, pharmaceutical companies recognize the importance of selecting the right partner for HPAPI manufacturing, development, packaging, and commercialization of products.
Some companies work with one contract development and manufacturing organization (CDMO) throughout the entire life cycle, while others partner with multiple vendors. To ensure success, teams must conduct due diligence to identify CDMOs that meet their safety, technology, process, economic and schedule requirements.
A panel of experts discussed the key areas for consideration and best practices when outsourcing HPAPI development, manufacturing and packaging to a CDMO.
To download this whitepaper: Choosing The Right CDMO For HPAPI Development, Manufacturing & Packaging (White Paper – PDF)
We provide a complete range of HPAPI Manufacturing Services and we are committed to supporting clients at every stage of the manufacturing cycle, delivering best-in-class services efficiently and effectively.
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