The REMEDI GMP Facility is a state of the art cGMP facility, where clinical trial product will be manufactured. The facility has a floor space of 250m2 and consists of two parallel production suites. Each suite consists of three EU cGMP Annex 1 certified Grade B production cleanrooms, with Grade A isolators within each. Each room is equipped with fully validated equipment, necessary for the production of the clinical products. Each suit is controlled by separate air handling units and so this can facilitate the production of two different products in each suite at the same time.

The facility aims to bring the research work carried out in the REMEDI laboratories and translate this research into clinical product. The main disease focuses are Osteoarthritis, Diabetes and Peripheral Vascular Disease.

The Facility has been funded by Science Foundation Ireland (SFI) and also The Higher Education Authority (HEA).

The facility has a full team of qualified staff:

Director: Professor Timothy O’Brien

Scientific Director: Professor Frank Barry

Quality Person: Geraldine Walsh

Quality Manager: Marc Eglon

Production Manager: Aoife Duffy

Facility Manager: Dr Karen Duffy

Facility Engineer: Alan Leahy (Vector FM)

Six Production Operators

For further information contact:

Dr. Karen Duffy
Facility Manager

Tel: + 353 91 495326
Fax: + 353 91 495547
Email: karen.duffy@remedi.ie

Prof. Timothy O' Brien,
Facility Director

Tel: +353 91 495166
Fax: +353 91 495547
Email: timothy.obrien@remedi.ie