MIAS Pharma Ltd is the brainchild of Ann McGee, a former Senior Inspector with the Irish Competent Authority (HPRA). Ann founded MIAS Pharma Ltd to build on her vision of accelerating and innovating compliant patient care.
With the exceptional growth of the biopharmaceutical sector across the globe, we act as a catalyst to make Europe an accessible market for new medicines in the most time efficient/cost effective manner.
Our team of Qualified Persons (QP) and quality professionals, with over 70 years combined industry experience, has a proven track record of client delivery.
Mary Hendrick, Consultant
A Qualified Person/Quality Consultant with
almost 20 years’ experience in the pharmaceutical industry, Mary has gained
considerable experience in the areas of processing, laboratory, Regulatory
Affairs, Quality Assurance, Compliance and Qualified Person batch release
activities in the medicinal product and medical device areas. She has extensive
knowledge and experience in the areas of PQR, change control, deviations,
complaints handling, stability and auditing.
Mary has significant experience in the quality oversight of global
contract manufacturing organizations responsible for sterile injectables,
liquids/gels and solid oral doses for US, EU and rest of world markets.
Prior to becoming an independent
consultant, Mary held the role of Qualified Person with Endo Ventures, where
she was responsible for the QA management of Endo’s Contract Manufacturing
Organizations, while also having responsibility for product release in both US
and EU markets.
Mary spent several years as the Qualified
Person with Paladin Labs Europe Ltd (formerly Labopharm Europe Ltd) where she
worked closely with the Senior Director of Quality in quality assurance reviews
and batch dispositions.
Mary holds a MSc Pharmaceutical
Manufacturing Technology (Qualified Person) from Trinity College Dublin and
also a BSc. (Hons) Applied Sciences (Physics & Chemistry) from DIT Kevin
Street/Trinity College Dublin.