Published July 2000
| Version v1
Report
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Approaches to the design of clean air handling facilities for radiopharmaceuticals
Creators
Description
Manufacturing, handling and administering processes of radiopharmaceuticals have to meet the requirements of both the fields viz. ''radio'' activity and ''pharma'' activity. Both these fields often dictate conflicting requirements. A step by step analysis of these conflicts can lead to practices reasonably acceptable to both the fields. The design approaches include engineering concepts of radiation protection, concepts and practices for pharmaceuticals, biologically unsafe products/processes and manufacturing, handling and administering processes of radiopharmaceuticals
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32028755.pdf
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Additional details
Publishing Information
- Imprint Title
- Report of the consultants meeting on good manufacturing practices and clean room requirements for radiopharmaceuticals
- Imprint Pagination
- 26 p.
- Journal Page Range
- p. 12-17
- Report number
- INIS-XA--396
Conference
- Title
- Consultants meeting on good manufacturing practices and clean room requirements for radiopharmaceuticals
- Dates
- 24-27 Jul 2000
- Place
- Vienna (Austria)
INIS
- Country of Publication
- International Atomic Energy Agency (IAEA)
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 32028755
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE; S38: RADIATION CHEMISTRY, RADIOCHEMISTRY AND NUCLEAR CHEMISTRY;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- CHEMICAL PREPARATION; CLEAN ROOMS; HOT LABS; LABORATORY EQUIPMENT; MANUFACTURING; NUCLEAR MEDICINE; RADIATION PROTECTION; RADIOPHARMACEUTICALS; TRACER TECHNIQUES
- Descriptors DEC
- DRUGS; EQUIPMENT; ISOTOPE APPLICATIONS; LABELLED COMPOUNDS; LABORATORIES; MATERIALS; MEDICINE; NUCLEAR FACILITIES; RADIOACTIVE MATERIALS; SYNTHESIS
Optional Information
- Notes
- Presentation by Mr. P.B. Kulkarni; 3 figs