Published July 2000 | Version v1
Report Open

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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Part of:
Report of the consultants meeting on good manufacturing practices and clean room requirements for radiopharmaceuticals

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