"We have taken biopharmaceuticals from early concept studies all the way to market approval."

Mrs Alison Justice

Quality Assurance Director

alison.justice@edenbiodesign.com

Alison’s role is to ensure Eden Biodesign’s systems and procedures are compliant with the cGMP requirements applicable for the design, development and delivery of clinical trials materials.

Alison has held a variety of QC/QA roles within pharmaceutical, fine chemical and medical device contract manufacturing organisations. Alison is an experienced Quality System auditor familiar with quality management system requirements for Pharmaceutical, Medical Device and Active Pharmaceutical Ingredients manufacture.

Prior to joining Eden Biodesign, Alison was Quality Manager at an AIM listed wound care company where she successfully implemented ISO13485:2003 and provided support to several successful FDA submissions.