Search results - 7 results

Characterization and risk identification of falsified medicines and adulterated dietary supplements

selectivity and specificity for the detection of targeted plants in mixtures. It stands to reason that collaborations on these topics would be beneficial for both the European and the Chinese policy makers to ...

Characterization and hazard identification of substandard and falsified antimicrobials encountered in Belgium

characterization of SF-antimicrobials, collected samples were also evaluated in terms of impurities and dissolution. The impurities were analyzed based on the methods of the European Pharmacopoeia (Ph. Eur.) and the ...

API Testing: how OMCLs can support the control of APIs

Publication Type: Scientific poster, presentation or proceeding Authors: Eric Deconinck; Yvan Grange Source: EDQM and European Pharmacopoeia: State-of-the-art Science for Tomorrow’s Medicines, EDQM, ...

Regulatory issues regarding manufacture and control of vaccine adjuvants. The EU situation.

at batch release Belgian Change Clinical clinical trial Clinical trials Combination Components Control developing Development distribution EU European future Group Guidelines health Hepatitis Hepatitis ...

Implementation over the past 20 years of the 3R's principle for batch release at the Scientific Institute of Public Health, Belgium (IPH).

eighties of last century; the European Pharmacopoeia has invested time and effort in the reduction, the replacement and the refinement of animal tests, better known as the 3R's principle.During the past ...

Non-sterile pharmaceutical water: source of life and/or potential carrier for opportunistic pathogens

water quality might be required. The European pharmacopoeia provides quality standards for water for injections (WFI), purified water or water for preparation of (herbal) extracts. It stands to reason ...

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