Recommendations for evaluating the safety of medicinal products containing nanoparticles
Recommendations for preclinical safety assessment of medicinal products containing nanoparticles are presented. The recommendations provide conditions for research acute and chronic toxicity of nanotherapeutics, methods for their quantitative and qualitative assessments.
Main Authors: | R. N. Alyautdin, B. K. Romanov |
---|---|
Format: | Article |
Language: | Russian |
Published: |
Ministry of Health of the Russian Federation, Federal State Budgetary Institution «Scientific Centre for Expert Evaluation of Medicinal Products»
2018-02-01
|
Series: | Безопасность и риск фармакотерапии |
Subjects: | |
Online Access: | https://www.risksafety.ru/jour/article/view/25 |
Similar Items
-
The distribution of fullerene n anoparticles in the body in preclinical studies
by: R. N. Alyautdin, et al.
Published: (2018-02-01) -
Guidelines for the Preparation of a Document Containing the Drug Safety Monitoring Results
by: Yu. V. Olefir, et al.
Published: (2018-02-01) -
Practical recommendations for screening of information on the drug safety
by: E. Yu. Pasternak, et al.
Published: (2018-02-01) -
Guidelines for the planning and implementation of pharmacovigilance systems audit
by: S. V. Glagolev, et al.
Published: (2018-02-01) -
Recommendations on the procedure for determining the interchangeability of medicinal products
by: B. K. Romanov, et al.
Published: (2018-02-01)