In line with its British Accreditation provider (UKAS), QAICL has concluded that there should be no change to required policies or practice as regards the outcome of Brexit as the standards to which QAICL offer registration are both customer and market led. It is possible that cross border accreditations that relate directly to EU Regulations (such as those under ISO 13485 for Medical Devices), may require some adjustment to take account of any agreed arrangements following exit from the EU. However, any such adjustments necessary will be made by QAICL during audits, to take account of customer specified requirements and … Continue reading Brexit statement