AN OVERVIEW OF THE MAIN CHANGES IN THE RULES OF GOOD LABORATORY PRACTICE (THE ORDER FROM 01 APRIL 2016 № 199n ENTERED INSTEAD OF THE ORDER OF MINISTRY OF HEALTH OF 23 AUGUST 2010 №708n)
This article provides an overview of the changes in requirements, processes, organization, planning, conducting and quality control of preclinical studies medicines, as well as making their results and archiving, approved by order of Ministry of Health of the Russian Federation from 01 April 2016 N...
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| Format: | Article |
| Language: | Russian |
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LLC Center of Pharmaceutical Analytics (LLC «CPHA»)
2019-01-01
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| Series: | Разработка и регистрация лекарственных средств |
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| Online Access: | https://www.pharmjournal.ru/jour/article/view/341 |
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| author | M. S. Zhuravleva M. V. Lebedeva |
| author_facet | M. S. Zhuravleva M. V. Lebedeva |
| author_sort | M. S. Zhuravleva |
| collection | DOAJ |
| description | This article provides an overview of the changes in requirements, processes, organization, planning, conducting and quality control of preclinical studies medicines, as well as making their results and archiving, approved by order of Ministry of Health of the Russian Federation from 01 April 2016 N 199n. |
| format | Article |
| id | doaj-art-e5b9ed23c81840579fe3244a47818368 |
| institution | DOAJ |
| issn | 2305-2066 2658-5049 |
| language | Russian |
| publishDate | 2019-01-01 |
| publisher | LLC Center of Pharmaceutical Analytics (LLC «CPHA») |
| record_format | Article |
| series | Разработка и регистрация лекарственных средств |
| spelling | doaj-art-e5b9ed23c81840579fe3244a478183682025-08-20T03:19:32ZrusLLC Center of Pharmaceutical Analytics (LLC «CPHA»)Разработка и регистрация лекарственных средств2305-20662658-50492019-01-0101212215341AN OVERVIEW OF THE MAIN CHANGES IN THE RULES OF GOOD LABORATORY PRACTICE (THE ORDER FROM 01 APRIL 2016 № 199n ENTERED INSTEAD OF THE ORDER OF MINISTRY OF HEALTH OF 23 AUGUST 2010 №708n)M. S. Zhuravleva0M. V. Lebedeva1Independent testing center "OLPHARM"Independent testing center "OLPHARM"This article provides an overview of the changes in requirements, processes, organization, planning, conducting and quality control of preclinical studies medicines, as well as making their results and archiving, approved by order of Ministry of Health of the Russian Federation from 01 April 2016 N 199n.https://www.pharmjournal.ru/jour/article/view/341good laboratory practicemedicinechangesrequirementsreviewpreclinical studies |
| spellingShingle | M. S. Zhuravleva M. V. Lebedeva AN OVERVIEW OF THE MAIN CHANGES IN THE RULES OF GOOD LABORATORY PRACTICE (THE ORDER FROM 01 APRIL 2016 № 199n ENTERED INSTEAD OF THE ORDER OF MINISTRY OF HEALTH OF 23 AUGUST 2010 №708n) Разработка и регистрация лекарственных средств good laboratory practice medicine changes requirements review preclinical studies |
| title | AN OVERVIEW OF THE MAIN CHANGES IN THE RULES OF GOOD LABORATORY PRACTICE (THE ORDER FROM 01 APRIL 2016 № 199n ENTERED INSTEAD OF THE ORDER OF MINISTRY OF HEALTH OF 23 AUGUST 2010 №708n) |
| title_full | AN OVERVIEW OF THE MAIN CHANGES IN THE RULES OF GOOD LABORATORY PRACTICE (THE ORDER FROM 01 APRIL 2016 № 199n ENTERED INSTEAD OF THE ORDER OF MINISTRY OF HEALTH OF 23 AUGUST 2010 №708n) |
| title_fullStr | AN OVERVIEW OF THE MAIN CHANGES IN THE RULES OF GOOD LABORATORY PRACTICE (THE ORDER FROM 01 APRIL 2016 № 199n ENTERED INSTEAD OF THE ORDER OF MINISTRY OF HEALTH OF 23 AUGUST 2010 №708n) |
| title_full_unstemmed | AN OVERVIEW OF THE MAIN CHANGES IN THE RULES OF GOOD LABORATORY PRACTICE (THE ORDER FROM 01 APRIL 2016 № 199n ENTERED INSTEAD OF THE ORDER OF MINISTRY OF HEALTH OF 23 AUGUST 2010 №708n) |
| title_short | AN OVERVIEW OF THE MAIN CHANGES IN THE RULES OF GOOD LABORATORY PRACTICE (THE ORDER FROM 01 APRIL 2016 № 199n ENTERED INSTEAD OF THE ORDER OF MINISTRY OF HEALTH OF 23 AUGUST 2010 №708n) |
| title_sort | overview of the main changes in the rules of good laboratory practice the order from 01 april 2016 no 199n entered instead of the order of ministry of health of 23 august 2010 no708n |
| topic | good laboratory practice medicine changes requirements review preclinical studies |
| url | https://www.pharmjournal.ru/jour/article/view/341 |
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