CQV

(Commissioning - Qualification - Validation)

Commissioning, qualification and validation of equipment and processes

When the schedule is tight, an efficient process is essential. We support you with a structured and professional implementation of your CQV activities, so that the project stays on track without compromising quality or compliance.

We offer comprehensive support for the implementation and optimization of new and existing equipment. Our assistance covers the entire process – from support to the design phase and FAT activities, to installation on site, as well as commissioning and carrying out various qualification activities. In addition, we are happy to take care of the development of processes, including Cycle Development and the subsequent initial validation.

We also assist with the design of various requirements documents such as URS and CARA, etc., as well as the implementation of quality risk analyses. Through a systematic approach, we ensure that the documentation is tailored to your specific needs and complies with applicable standards and regulatory requirements.

Rune Gerfort

Founder of Danval ApS and freelance pharma consultant

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We perform consultancy work with quality at the center and are your shortcut to compliance from start to finish.

+ 20 years of experience in pharma production

Flexible collaboration regarding project plan

Experience from many projects

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Rune Gerfort

Grundlægger af Danval ApS og freelance pharma-konsulent

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Rune Gerfort

Founder of Danval ApS and freelance pharma consultant