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 drugs and dietary supplements