Glide™ Technology | Quality Systems
It is the policy of Glide Pharma to always supply products and services to our customers that conform exactly to stated or agreed specifications and meet the needs and expectations of those customers.
Glide Pharma has been audited and obtained third party certification by a UK Notified Body against the ISO13485:2003 standard.
Medical devices manufactured or distributed by Glide Pharma in the EEA will meet the requirements of the Medical Device Directive 93/42/EEC and carry the CE Mark.
Our ongoing quality objectives are to provide complete customer satisfaction whilst continually seeking to improve our products and service by the regular analysis of appropriate measures of process performance.
The quality management system is regularly reviewed by the CEO to ensure its efficiency and effectiveness in meeting the company's objectives and is implemented and maintained by the strict observance to the authorized quality manual and operating procedures.
