Clinical studies
Conducting bioequivalence studies and early phase clinical trials
- 01 Pharmacokinetics of small molecules
- 02 Pharmacokinetics of biotechnological preparations
- 03 Pharmacodynamics of biotechnological preparations
- 04 Immunogenicity of biotechnological preparations
- 05 Central laboratory (safety and efficacy parameters)
- 06 Statistical processing (BE, I, II, III phases)
- 07 Comparative Dissolution Kinetics Test (CDK)
- 08 Biowaiver
- 09 Preparation of laboratory kits for conducting clinical trials
- 10 Provision of specific reagents, consumables
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
01
Pharmacokinetics of small molecules
02
Pharmacokinetics of biotechnological preparations
03
Pharmacodynamics of biotechnological preparations
04
Immunogenicity of biotechnological preparations
05
Central laboratory (safety and efficacy parameters)
06
Statistical processing (BE, I, II, III phases)
07
Comparative Dissolution Kinetics Test (CDK)
08
Biowaiver
09
Preparation of laboratory kits for conducting clinical trials
10
Provision of specific reagents, consumables
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