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Top Contract research organisations (CRO) . Listing

Phoenix Clinical Research Berytech Technology & Health Damascus Road, Beirut-Lebanon mobile : + 961 3 672 310 (Dr. Georges Labaki) office number: + 961 1 429 566 [email protected] website – https://www.phoenix-cr.com/ _______________________ Contract research organisations (CRO) by Peter Hogg ProClinical Life Sciences have become essential to the pharma, biotech, and medtech Leer más

clínica emcel

幹細胞療法在兒童疾病中的劑量與安全性分析

**幹細胞療法在兒童疾病中的劑量與安全性分析**

幹細胞療法在兒童疾病治療中展現潛力但劑量與安全性至關重要本分析探討了兒童臨床試驗中的幹細胞劑量範圍和安全性狀況為臨床應用提供指導研究發現不同疾病細胞類型和給藥方式影響著最佳劑量而安全性問題主要集中在免疫反應和腫瘤形成風險這些見解有助於優化治療方案確保兒童患者的安全性

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幹細胞療法在自閉症患者中的應用劑量設定

幹細胞療法在自閉症患者中的應用劑量設定至關重要本文分析了不同幹細胞類型患者年齡和自閉症嚴重程度對最適劑量的影響文章提出了基於患者特徵的劑量調整建議以最大化治療效果同時最小化副作用深入了解劑量設定有助於優化幹細胞療法在自閉症治療中的應用

células madre españa

幹細胞在肝腫瘤治療中的最佳劑量探索

幹細胞治療肝腫瘤的劑量優化至關重要本文通過系統回顧和薈萃分析探討了不同類型幹細胞的最佳劑量範圍研究發現間充質幹細胞的最佳劑量為 (1-5)×10^6 個/kg而肝臟幹細胞和誘導性多能幹細胞的最佳劑量範圍分別為 (1-2)×10^6 個/kg 和 (0.5-1)×10^6 個/kg這些劑量範圍可提供最佳的腫瘤抑制效果同時最小化不良反應

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Good Clinical Practice

Good Clinical Practice

Description

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

EU:

Adopted by CPMP, July 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

FDA:

Published in the Federal Register, 9 May 1997, Vol. 62, No. 90, pag. 25691-25709

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