干细胞疗法

Надлежащая производственная практика (cGMP)

Надлежащая производственная практика (cGMP) Целевая аудитория Курс предназначен для всех ученых (управленческий и лаборатории) и профессионалов в области биотехнологий, биофармацевтической, устройство, косметической, фармацевтической промышленности и агрохимикатов, чья работа функции, связанные с наркотиками / биологических 阅读更多…

NBScience
审核员 GCP

审核员, GCP

审核员, GCP Responsibilities The GCP Auditor is responsible for quality assurance auditing of all activities subject to the, “ICH 良好临床规范: 综合指南,” (GCP), 支持质量保证计划 (质量保证) to ensure that 阅读更多…

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anesthesia conferences

Medical meetings in Ukraine

Today we have analyzed the popularity of medical conferences in Ukraine. Yes, may be it’s not such popular conferences, but level of training of lecturers and level of knowledge gained at conferences in Kiev is very high. Also interested in the existence of various social programs organized by the company NBScience (interview with 阅读更多…

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临床研究

良好的临床实践

良好的临床实践

描述: 
The tripartite harmonised ICH Guideline was finalised underStep 4 in May 1996. This Good Clinical Practices document describes the responsibilities and expectations of all participants in the conduct of clinical trials, including investigators, monitors, sponsors and IRBs. GCPs cover aspects of monitoring, reporting and archiving of clinical trials and incorporating addenda on the Essential Documents and on the Investigator's Brochure which had been agreed earlier through the ICH process.
Implementation
Step 5
我:
Adopted by CPMP, 七月 1996, issued as CPMP/ICH/135/95/Step5, Explanatory Note and Comments to the above, issued as CPMP/768/97
MHLW:
Adopted March 1997, PAB Notification No. 430, MHLW Ordinance No. 28
食品药品监督管理局:
Published in the Federal Register, 9 可能 1997, Vol. 62, No. 90, p. 25691-25709
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NBScience
GCP证书

GCP证书

сертификат для специалистов по клиническим исследованиям https://nbscience.com/gcpsertifikat/

NBScience
干细胞疗法