QUALITY AND REGULATORY
Avicenna Surgical Limited have a strong commitment to ensuring all our products and operational processes are compliant with the following quality and regulatory standards
All products supplied by Avicenna Surgical conform to EU Directive 93/42/ EEC (MDD) and we are in the process of fully migrating all certification to the new Medical Device Regulations 2017/745 (MDR), following Brexit we are also in the process of applying UKCA accreditation to all of our products. All new applications and certification transfers will be completed by the end of 2021 well before the deadlines set out by the EU and MHRA, ensuring Avicenna Surgical continues to remain in a strong position to service our customers requirements.
We have a dedicated in-house quality and regulatory team ensuring that all our staff are trained on regulatory matters and periodic internal audits ensure complete adherence to our quality systems and the ever changing regulation in this industry.