Frontier Therapeutics operates a quality management system which complies with the requirements of BS/ ISO 9001:2000 and all Repose products are manufactured to this standard.

The Repose range of pressure relieving products comply with Medical Devices 93/42/EEC and are marked as a Class 1 device.

Repose products also satisfy:

BS 4875-1:1985 Strength and stability of furniture. Requirements for the strength and durability of the structure of domestic seating.

We also comply with fire testing regulations as shown below:

BS 5852:1990 Methods of test for assessment of the ignitability of upholstered seating by smouldering and flaming ignition sources.

BS 6807:1996 Methods of test for assessment of ignitability of mattresses, upholstered divans and upholstered bed bases with flaming types of primary and secondary sources of ignition.

BS 7175:1989 Methods of test for the ignitability of bedcovers and pillows by smouldering and flaming ignition sources.

ISO 13485:2016 Medical Devices Quality Management Systems
Quality Management System for companies required to demonstrate their ability to provide medical devices that consistently meet client and regulatory requirements. 


Frontier recognises that sustainability is core to good business practice and believes that our business performance will improve in line with our enhanced focus on sustainability.

Frontier is accredited to ISO9001 and ISO14001, reflecting the excellence of the product design and manufacturing systems whilst continually assessing and actively working to minimise waste throughout the life-cycle of the product.

The management and all who work within Frontier are committed to the care of the environment and the prevention of pollution. The company ensures that all its activities are carried out in conformance with the relevant environmental legislation.