Clinical studies
Conducting bioequivalence studies and early phase clinical trials
- 01 Pharmacokinetics of small molecules
- 02 Pharmacokinetics of biotechnological drugs
- 03 Pharmacodynamics of biotechnological drugs
- 04 Immunogenicity of biotechnological drugs
- 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 drugs
03
Pharmacodynamics of biotechnological drugs
04
Immunogenicity of biotechnological drugs
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
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01
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02
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Клинические исследования
03
Проведение исследований биоэквивалентности и ранних фаз клинических исследований
Фармацевтический анализ лекарственных препаратов и БАД
04
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