Quality
GLP is a quality system concerned with the organisational process and the conditions under which non-clinical studies are planned, performed, recorded, archived and reported. RDDT define the roles of the Test Facility Manager, Study Director, Study Personnel, Quality Manager, and Quality Assurance personnel according to the Principles of GLP. The Quality Manual, standard Operating Procedures (SOPs), and the Quality Assurance program ensure that the RDDT conduct the studies and develop quality test data at the international level.
The test data generated by RDDT are compliant with national and international registration authorities including FDA, ICH, Australia registration authorities TGA (pharmaceutical), NRA (veterinary and agricultural chemicals), and the NICNAS (industrial chemicals).
Accreditations
RDDT has National Association of Testing Authorities, Australia (NATA) recognition as a laboratory conducting studies according to the OECD Principles on Good Laboratory Practice (GLP).
RDDT's laboratories operate under quality guidelines of OECD Principles of Good Laboratory Practice (GLP) and ISO 17025. RDDT's facility includes several laboratories with functions of: cell culture, bacterial culture, bio-analytical, test article formulation, histopathology and clinical pathology, etc. In addition, there is a GLP animal facility fully owned by RDDT.
For more information on OECD and GLP accreditation and compliance, visit www.nata.asn.au
Facility No: 15050
Corporate Site No: 15486