Today’s pharmaceutical companies must manage tight timelines and high demand for products, as well as shifting regulatory requirements and an increasingly complex global supply chain. How can contract development and manufacturing organizations (CDMOs) rise to this challenge and provide the support they need?
In this podcast with PharmaSource, Tommy Shornak, Senior Vice President, Sterile Injectables, discusses the steps that Kindeva is taking to become a world-leading proactive partner, offering comprehensive CDMO services to companies navigating a complex outsourcing landscape.
At the core of the strategy is a $200 million investment in our state-of-the-art Bridgeton facility, which delivers comprehensive sterile fill finish capability as well as long-term regulatory compliance. With fully Annex 1-compliant infrastructure and four automated filling lines, Bridgeton enables Kindeva to prepare proactively for tomorrow’s market needs.
Tommy also covers other ways that Kindeva is positioning itself as a one-stop partner for drug sponsors, including:
- Developing a no-single-source strategy to manage supply chain uncertainty
- Adopting data transparency in partnerships
- Evolving commercial models to provide sponsors with added flexibility
- Integrating sustainability into daily operations
He also discusses what true partnership looks like in practice and what CDMOs need to do to separate themselves from competitors over the next few years.
Listen to the podcast to discover how Kindeva is setting a new standard for proactive, flexible CDMO partnerships.
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