CORE--QUALITY SERVICES
核心——优质服务
基本信息
- 批准号:6424518
- 负责人:
- 金额:$ 5.34万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-02-23 至 2002-01-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
CORE D
The proposed projects (I, II, and III) all require the production of
injectable substances for treatment diagnosis in human subjects. To
ensure that these materials are safe, effective, and pure; an effective
quality assurance and quality control program is required by federal
regulations and must be instituted. We request personnel and supplies as
a core support for the following:
1. Analysis of raw materials, intermediate products, and final products
for identity, stability and purity as required by the Good Manufacturing
Practices (GMP) sections of the Code of Federal Regulation Analyses
include identity verification, sterility, bioburden assessment, endotoxin
contamination , mycoplasma contamination, flow cytometry analysis, and
potency testing. Review analyses and production records to assess the
suitability of each production lot for human clinical trials.
2. Microbiological monitoring of the production facilities to ensure that
cleaning, sanitization, and air quality systems are operating effectively.
3. Perform process validation and equipment certification and calibration
to ensure that production processes are under control and operate
reliable.
4. Provide documentation support, including the writing, reviewing, and
control of investigation New Drug Applications (IND), Master and
Production Batch Records, Standard Operating Procedures, Specification
Analytical Procedures, Labeling, and Validation Reports.
核心D
项目成果
期刊论文数量(0)
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会议论文数量(0)
专利数量(0)
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