DRUGS AND DRUG INGREDIENT TESTS
Drugs and drug ingredients testing are the sampling, examining technical standards and conducted tests to determine whether drugs/drug ingredients meet acceptable standards of quality then decided to accept or reject it.
ROLE OF DRUG/DRUG INGREDIENT TESTS:
- To prove with the customer and the state administration about the product quality of the business meets the specification, technical regulations respectively.
- Helping the business to provide suitable solutions to adjust if the results are not reached.
PROFESSIONAL CAPACITY
BE analysis center – AQP research and control pharmaceutical J.S.C was accredited by the Ministry of Health to meet Good Laboratory Practice (GLP) standard for the first time in April 2011 and periodic examinations meet the GLP standard. The center has been equipped with many modern machines and equipment for analysis and testing such as: HPLC, LCMS, UV-VIS, solubility tester….. with high sensitivity and accuracy. The staff, mostly young, highly qualified, well – trained, regularly participating in interlaboratory proficiency testing programs organized by leading institutes such as the national institute of drug quality control, Institute of Drug Quality Control Ho Chi Minh city. The results of all tests have achieved high accuracy, proving analytical capacities of the center are increasingly confirmed.
LIST OF ACCEPTED TESTES:
- Qualification by chemical methods.
- Qualification and quantification by the visible and ultraviolet absorption spectroscopy.
- Test of content uniformity.
- Test of iniformity of dosage units.
- Test of solubility of Solid Dosage Forms.
- Quantification of pharmaceutical substances and metabolites in biological fluids by liquid chromatography.