GMP Training Ltd was established in 1989 and is based in Co. Kildare, Ireland and specialises in the provision of training, auditing and consultancy in Good Manufacturing Practices (GMP) to meet FDA and EU Regulations. Our personnel have technical qualifications and extensive experience in the implementation of GMP in manufacture, QA and the laboratory. GMP Training Ltd keeps up-to-date with regulatory developments to ensure that we can assist our clients in compliance with FDA and EU GMP Regulations.
Director: Gemma O’Dwyer BSc (hons), MSc, M.I.I.T.D, I.R.C.A.
Gemma has worked in Q.C., Q.A. and Technical Services in companies manufacturing bulk pharmaceuticals (Eli Lilly), and medical devices (Amicon Irl.), both based in Ireland and her areas of expertise include GMP Training, GDP Training and GMP for the laboratory. Gemma has worked as a Production Manager at Leo Laboratories (finished pharmaceuticals) and has lectured in Health Care Technology at the D.I.T. Gemma is an accredited auditor with the International Register of Certified Auditors (IRCA), a member of the Irish Institute of Training & Development (IITD) a member of the Parental Drug Association (PDA) and of the Technical Industrial Pharmacists and Pharmaceutical Scientist association (TIPPSA).
Gemma's areas of expertise include:
» GMP Training
» GDP Training
» GMP for the laboratory
» Validation
» Aseptic Processing
» Auditing
Consultant: Jean Ryan BSc (hons)
Jean has worked for 12 years at Schering-Plough Brinny in Q.C., Technical Services, and Validation and as a Production Manager. Jean currently works in the area of facility design and validation and as a trainer and consultant for pharmaceutical and medical device manufacturers.
Jean's areas of expertise include:
» Validation
» Aseptic Processing
» Biotechnology
» GMP Training
» Plant Design & Layout
Consultant: Maeve Enright BSc (hons)
Maeve has worked in QC and QA for 16 years at Stafford Miller, Wyeth Medica, Rice Steele and Waterford Pharmaceuticals. Maeve currently works as a trainer and consultant with Pharmaceutical and Medical Device manufacturers.
Maeve's areas of expertise include:
» GMP for the laboratory
» Chemical Analysis
» Laboratory Quality Systems
» Validation
» GMP