Better Validation for CDMOs & Their Customers

Contract manufacturers in life sciences, whether CDMO or CMO, face extensive validation challenges across the entire development and manufacturing lifecycle, from development to technology transfer, manufacturing and handover.

Excellence in data integrity, quality and efficiency poses a competitive advantage

Assuring data integrity, quality, and efficiency for customers from technology transfer to and mounting pressures, from competing for contracts through to final delivery. To solve them, you need to understand them, you also need some help.

In this webinar, Kneat’s digital validation expert Mo Brar leans on his extensive experience working within CDMOs to demonstrate why validation is the secret competitive advantage to solving systemic issues in development and production and realizing more ROI for the organization.

Attend to Learn:

• Key validation challenges for CDMOs, including compliance, cleaning validation, CQV, and more.
• How to avoid common document errors that cause data integrity issues and non-compliance.
• How to effectively manage extensive and detailed validation documentation.
• How to improve technology transfer, electronic batch records, and SOP accessibility to streamline validation and production.

Presented by:

Mo Brar, Process Engineer, Kneat