Remove Communication Remove Pharmaceutical Manufacturing Remove Process Improvement
article thumbnail

Corrective and Preventive Action (CAPA) Procedure for GMP

GMPSOP

Immediately communicate the incident to stakeholders and initiate an internal laboratory investigation. For instance, you can undertake a list of process improvement works targeting the elimination of causes that have resulted in the defect. No, this will be a violation of good laboratory practice.

article thumbnail

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

Drug Patent Watch

Clear Communication is Key Establish clear channels of communication from the outset. Managing Quality and Compliance Quality and regulatory compliance are non-negotiable in pharmaceutical manufacturing. Ensuring Data Integrity Data integrity is paramount in pharmaceutical manufacturing.