Q MEN's fundamental orientation is to be recognized for quality in the medical device industry.
Our aim is,
- To serve as a competent consultancy firm within the scope of Medical Device Regulation, In Vitro Diagnostic Medical Device Regulation (MDR/IVDR), GMP, cosmetic regulations in the world and in our country,
- As your reliable and respected solution partner, we aim to save you time and money without compromising on quality, based on the principle that success lies in the details.
- Achieving excellence in customer satisfaction with the principle of zero error,
- To be consultants and trainers with exemplary practices in the sector by adopting the principles of continuous improvement of the ISO 9001: 2015 and ISO 13485: 2016 Quality Management System as a policy,
- To support healthcare service providers and medical device manufacturers with simple, understandable concepts and practices in line with the needs of organizations and in line with national and international laws, regulations and standards.
Qualified personnel resources, effective use of technology and experience, professionalism in cooperation with customers are our competencies. We focus on customer satisfaction by making these competencies measurable with the Quality Management System.
Our vision,
To be one of the future strategic solution partners of manufacturers operating in the sector with the increasing share of science and technology in health and medical device production.
Our values;
To protect privacy and confidentiality,
To catch the future together with organizations as long-term solution partners,
Analyzing scientific data with a professional team,
Our main goal is to comply with the deadlines of the projects we are a partner of.
Our slogan is “LONG LIVE QUALITY”.
