Since 2006, VALTEC GmbH has been advising and supporting companies in the pharmaceutical industry, medical technology, biotechnology, and assisted reproductive technology.

The main focus is on quality management, qualification of facilities, equipment, and environmental conditions, as well as validation of processes and procedures. Ensuring GxP compliance, preparing, conducting, and following up on audits and inspections, as well as the continuous improvement of existing processes and systems, are additional core competencies of VALTEC GmbH.

VALTEC GmbH also assists companies in obtaining permits and approvals according to AMG. The creation of requirement-specific and GxP-compliant documents, as well as conducting training sessions and workshops, complement the service portfolio of VALTEC GmbH.

The focus is always on the specific requirements and circumstances of the customer to achieve the best possible and successful outcome for each task or project situation together.