Development, validation and testing of ND methods
Conducting development, validation and testing of methods for quantitative content of the active substance, authenticity, homogeneity of dosage, impurities and dissolution for regulatory documentation.
Conducting specialized consulting with proofreading of regulatory documentation, as well as independent control of methods of regulatory documentation before submitting a dossier for a medicinal product.
9
chromatograph mass spectrometers
that allow for high-precision determination of low-molecular compounds in biological samples
500+
research
on bioequivalence and pharmacokinetics of medicinal products implemented by the laboratory
ISO 9001
Management System
is certified for compliance with the standard of Good Laboratory Practice (GLP) principles
Other services within the scope of the direction pharmaceutical analysis of medicines and dietary supplements
See also
Preclinical studies
01
Conducting pharmacokinetic studies on animals
Clinical studies
02
Conducting bioequivalence studies and early phase clinical trials
Pharmaceutical analysis of medicines and dietary supplements
03
Development and validation of regulatory documentation methods: authenticity, quantitative content, dosing homogeneity, impurities, dissolution