MIAS Pharma Limited
Eleanor Loughman is an experienced professional in the pharmaceutical industry, currently serving as a Qualified Person at MIAS Pharma Limited since April 2023. Prior to this role, Eleanor held key positions including Senior Manager QA Manufacturing/Qualified Person at Grifols, QA Manufacturing Manager at GRIFOLS WORLDWIDE OPERATIONS, and QA Lead at Mallinckrodt Pharmaceuticals. Additional experience includes roles as a Quality Specialist at MSD and Quality Systems Engineer at Tcoag. Eleanor's academic background includes an MSc in Industrial Pharmaceutical Technology from the Institute of Technology, Sligo, and a Master's degree in Pharmaceutical Sciences from Technological University Dublin, along with a degree in Microbiology from Trinity College Dublin.
This person is not in any teams
MIAS Pharma Limited
MIAS Pharma Limited is a company setup to facilitate pharmaceutical companies to import human medicinal product in to the European Market. As your European partner we can provide contract services which will enable you to import and batch release product into Europe in a compliant manner. MIAS Pharma Limited holds two MIAs (Manufacturing and Importation Authorisations) to cover medicinal products for human use in EU/EEA: 1. MIA for Investigational Medicinal Products (IMPs) 2. MIA for Commercial Products MIAS Pharma can also provide oversight of: 1. European Qualified Person (QP) services 2. Regulatory compliance of manufacturing activities 3. Regulatory compliance of Analytical Testing and Retesting 4. Regulatory compliance of Repackaging / Relabelling services 5. Regulatory compliance of Shipment and Transportation activities 6. Compliance with responsibilities as a Market Authorisation Holder (MAH)