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Best CDMO Practices for Startups: Navigating the Complex World of Contract Development and Manufacturing

Drug Patent Watch

Take the time to clearly define your technical needs, from drug substance manufacturing to packaging requirements. The CDMO Selection Process: A Step-by-Step Guide Selecting the right CDMO is a critical decision that can have long-lasting impacts on your startup’s success.

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Corrective and Preventive Action (CAPA) Procedure for GMP

GMPSOP

Immediately communicate the incident to stakeholders and initiate an internal laboratory investigation. In a packaging line, a printer was used to imprint manufacturing and expiry dates on a batch of empty cartons which will be used to fill tablet strips. No, this will be a violation of good laboratory practice.