Incorporated in 2007, No deviation is a patient-centric solution provider for the pharmaceutical industry. We are experts in engineering consultancy, commissioning, qualification and validation services, and regulatory quality/compliance in Asia and Europe.

No deviation offers personalised focused solutions for the pharmaceutical industry in engineering consultancy and regulatory quality and compliance. With a sharp focus on delivering value-adding commissioning, qualification and validation services, we are leading experts in developing the lean CQV methodology. We extend our offerings to GMP-certified software for environmental monitoring and contamination control, paperless validation, training and professional recruitment services.

The company places keen attention on patient safety, process understanding, regulatory compliance and efficiency in the areas of safety, quality, delivery and cost. 

At No deviation, we partner with you to help you with troubleshooting or your CAPA, executing your CQV process, or implementing new digital solutions. We believe in a holistic approach to achieving a successful execution derived from the principles of Understand, Observe, Define and Implement, which take its origin from ICHQ9. Whether as part of an integrated team, or overall scope management, the company delivers effective results from tapping into its team’s vast knowledge and experience in the field. 

Reach out to us to know more about paperless CQV, web-based EMS, or simply like-minded resources support. Visit our website at https://nodeviation.com/ to learn more about our services.

Health Care

Life Sciences

Pharmaceutical

No deviation

Pierre Winnepenninckx

Olivier Reynaert

David Bartlett

Dave O'Connor

The Engineering Team at No deviation is responsible for providing expert engineering consultancy and executing commissioning, qualification, and validation (CQV) services for the pharmaceutical industry. They focus on developing and implementing lean CQV methodologies, troubleshooting issues, and ensuring regulatory compliance. Their expertise extends to implementing GMP-certified software solutions for environmental monitoring, contamination control, and paperless validation. The team aims to enhance patient safety, process efficiency, and quality through a holistic approach based on ICHQ9 principles.

Engineering Team

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Team members