WQS Management Consultants is welcoming new colleagues in April 2026: Four new colleagues have joined our team as of April 1, 2026. Another will join on April 15. Together, they bring fresh expertise, new perspectives, and new capacity to the areas of medical device regulation where they are most needed today.
Strengthening two key areas
The new team members are working in the following key areas:
Regulatory Affairs & Quality Management (RA/QM)
Support with marketing authorization procedures, QM system development and maintenance, preparation for audits, and ongoing consulting on MDR and IVDR compliance.
Clinical Support
Preparation and review of clinical assessments, support with PMCF plans, clinical literature research, and documentation in accordance with current standards (e.g., MEDDEV 2.7/1 Rev. 4, MDCG guidelines).
The demands on medical device companies are increasing: MDR and IVDR compliance, complete clinical documentation, and more rigorous scrutiny by Notified Bodies. Our growth brings greater capacity, deeper expertise, and consistent quality.
Welcome to WQS
We look forward to working with you, to new perspectives, and to everything we will achieve together for our clients and partners.
