Upgrading an autoclave control system requires not only industrial automation expertise but also extensive experience in GxP compliance and validation.
To address this need, Qualipharma and Core Process offer a comprehensive solution that covers every stage of the project, from technology modernization to system qualification and validation.
Qualipharma, represented by Carlos Fernández, CSV & CSA SME, provides specialized support for the validation and qualification activities associated with autoclave control system upgrades. This includes defining a risk based validation strategy, executing qualification activities, and supporting process revalidation to ensure both the equipment and the computerized system remain in a validated state.
Core Process, represented by Bernat Villoro, Sales Director, delivers automation revamping projects by upgrading control platforms, hardware, and software to extend the operational life of existing equipment while supporting compliance with current regulatory requirements and improving safety, data integrity, and operational efficiency.
By combining their expertise, Qualipharma and Core Process provide an integrated approach that aligns technology modernization with the validation and regulatory requirements of GxP environments.
Are you considering upgrading your autoclave control system or assessing the feasibility of an automation revamping project?
Contact us at info@qualipharmagroup.com and our experts will be happy to help.
