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Integrating Process Analytical Technology (PAT) into validated GMP environments demands more than just technical know-how. Explore the critical role PAT plays in ADC manufacturing, highlighting the challenges and considerations that come with embedding it into GMP workflows.
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This webinar on Process Analytical Technology (PAT) provides valuable insights into its benefits for accelerating process development and its impact on the development and manufacture of novel conjugates. Leveraging an advanced Antibody-Drug Conjugate (ADC) platform and integrating PAT into development workflows enhance process efficiency and ensure the delivery of high-quality products from the start.
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Process Analytical Technology (PAT) plays a vital role in enhancing process control and deepening process understanding. In this webinar gain valuable insights into PAT implementation for ADC and bioconjugation processes, and how drug developers and manufacturers can access real-time insights into their process parameters and product attributes, enabling proactive adjustments and optimization.
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ADC AND BIOCONJUGATION CDMO SERVICES
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Antibody-drug conjugates (ADCs) have ignited a new era of targeted cancer therapies but there are several obstacles and complexities to overcome to bring these therapies to market. To solve the challenges and ensure success of your ADC project, you can rely on an industry-leading CDMO partner with 15+ years experience and focused expertise to meet your ADC development and manufacturing needs, from pre-clinical to commercial. Learn more.
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