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PROBE Analytical Laboratory |
Accreditations and GLP GMP Capabilities in the lab |
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The Intertek PROBE Australia laboratory provides an extensive range of testing to GLP, GMP and related protocols and standards. Expertise and laboratory capability help clients with research and routine testing projects. Expertise includes chemical and material analysis.
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PROBE Laboratory Accreditations:
GMP, Good Manufacturing Principles Laboratory:
- Approved under the Australian Therapeutic Goods Act (GMP-TGA) for the step of analysis & testing, covering all analyses including chromatographic & spectroscopic techniques.
NRA, National Registration Authority:
- License for the Manufacturing of Veterinary Products for the step of analysis & testing.
GLP, Good Laboratory Practice Laboratory:
- OECD Principles of Good Laboratory Practice (GLP) for the analytical component of non-clinical residue study & worker exposure trials (agricultural & veterinary chemicals).
NATA, National Association of Testing Authorities:
- Accredited Laboratory (Registration No. 3100) since 1990, covering analyses such as workplace Environment & Hazards, Pesticide Residues in Foods & Agricultural Materials, Residues in Constituents of the Environment (e.g. USEPA priority Pollutants in Waters & Soils).
Quarantine Registered Laboratory:
- Accredited EPA analyst available ISO9002 Certification
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PROBE Analytical Laboratory Services:
- Routine and non-routine analysis
- Manufacturing, Raw Materials Testing
- Stability Studies and Storage Facilities
- Changes in liquid formulations during storage
- OVI, Purity Check
- ID of contaminants
- Contamination measurement
- Trace levels of by-products by NMR, GCMS
- Detailed composition of raw materials from supplier's batches.
- Packaging, Migration Studies from packaging to contents
- Labeling glue, Printing ink,
Additive screens in new packages,
Package evaluation from new suppliers
- Final Product Testing
- Contamination, Impurities
- Unknown deposits identification
- Precipitates in 'formulation'
- High by-product level in raw material
quality control
- Limits testing
- Metals in final products
- Confirmation of formulation compositions
- Research, Method Development
- Method Validation, Method Validation Protocol
- Method Validation Report
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