The good laboratory practice and good clinical practice requirements for the production of radiopharmaceuticals in clinical research-Reference-Cited by-同舟云学术

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The good laboratory practice and good clinical practice requirements for the production of radiopharmaceuticals in clinical research

Published:2005-07 Issue:7 Volume:26 Page:575-579
ISSN:0143-3636
Container-title:Nuclear Medicine Communications
language:en
Short-container-title:

Author:

De vos Filip J.,De Decker Mario,Dierckx Rudi A.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Radiology Nuclear Medicine and imaging,General Medicine

Reference1 articles.

1. Eur J Nucl Med I;mag,2003

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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2. Implementation of Good Laboratory Practices (GLP) in basic scientific research: Translating the concept beyond regulatory compliance;Regulatory Toxicology and Pharmacology;2017-10

3. The Road to Excellence: A Case Study of the Application of GMP, ISO 9001 and the EFQM Excellence Model in a Nuclear Medicine Department;Quality in Nuclear Medicine;2016-11-16

4. Manufacturing of [14C]-Labeled Drug Substance and Drug Product Utilized in Clinical Research: A Case Study of Omecamtiv Mecarbil;Current Pharmaceutical Design;2016-01-26

5. Translation of Radiopharmaceuticals from Bench to Bedside: Regulatory and Manufacturing Issues;Radiopharmaceuticals for Therapy;2016

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