We are very pleased to announce that Henriette Vindmar has joined us 1. July, 2017 as our new Director for QA & QC and EHS.
Henriette graduated as M.Sc.Pharm. in 1990. Henriette has extensive experience within the quality area and compliance with current good manufacturing practice (cGMP) in the biotech and pharmaceutical industry related to Active Pharmaceutical Ingredients, Medicinal Products and Medical Devices. Furthermore, Henriette has been a Medicines Inspector at the Danish Medicines Agency as well as responsible for quality assurance in several previous positions and Qualified Person according to Directive 2001/83/EC. Henriette has also taken roles as GMP consultant and Auditor and has additionally been a speaker at seminars on general GMP, Quality Risk Management, Quality by Design, Qualification/Validation, Cleaning Validation and Audits.