Medical Device Services
We are the specialists to ensure you gain maximum benefit from your medical device quality management system.
Trust QCS to assist with the design and implementation of your system, the provision of effective audits and all your training requirements. With an enviable record for quality management delivery we are here to ensure you gain maximum benefit from having a medical device management system certified to ISO 13485:2016.
QCS has, for many years, been a leading provider of medical device consultancy, training and regulatory advice to businesses operating within the medical device, sterile and healthcare sectors. Our consultants have been involved in the regulatory aspects of new to market medical device innovations as well as supporting existing products in an ever more complicated regulatory framework.
We have the ability, experience and expertise to install a quality management system for your company – which can be used to allow you to demonstrate conformance with ISO 13485 as well as the FDA Code of Federal Regulation, title 21, Part 820.
The kinds of services we offer for medical device manufacturers include:
Why use QCS for training...
• CQI/IRCA Approved Training Partner for all auditor courses
• Ongoing investment in ALL courses
• Interactive Courses... involving you in the learning experience
• Highly trained and qualified industry experts
• Access at highest level in all sectors
• Competitive prices
• 100% guarantee