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Sterilization Validation and Routine Operation Handbook

Radiation

(Autor)

Buch | Hardcover
168 Seiten
2001
Crc Press Inc (Verlag)
978-1-58716-057-8 (ISBN)
CHF 129,15 inkl. MwSt
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Presents a framework for the validation and routine operation of an irradiation sterilization process. This work discusses methods to aid in comprehending the requirements in these standards. It also provides procedures for the validation and routine monitoring and control of specific gamma and electron beam radiation sterilization processes.
The validation and radiation sterilization process for biomaterials and medical devices requires careful planning to ensure regulatory compliance followed by precise accuracy in execution and documentation. This in-depth guide details all steps from prevalidation planning to final report and ongoing monitoring and control. Sterilization Validation & Routine Operation Handbook: Radiation provides a framework for the validation and routine operation of an irradiation sterilization process. The guidance presented complies with ANSI/AAMI/ISO 11137: 1994, Sterilization of health care product-Requirements for validation and routine control-Radiation sterilization and the newly published AAMI substantiation of 25 kGy using VDmax procedure. The author discusses methods to aid in comprehending the requirements in these standards. She also provides practical procedures for the validation and routine monitoring and control of specific gamma and electron beam radiation sterilization processes.

Background chapters provide needed information on radiation sterilization technologies, sterilization microbiology, validation approaches and working with a radiation sterilization contractor. Much of the information in this new book is presented in convenient tables and charts, with diagrams and other schematics that simply illustrate appropriate validation methodologies. Sterilization Validation & Routine Operation Handbook: Radiation brings together in one resource information scattered throughout many documents and will be useful to all those involved in the sterilization of medical materials, drugs and devices.

Rationale for Validating Sterilization Processes
Characterization of Radiation Processes
o Physical Characteristics of Radiation
o Facility Design
o Effects of Radiation on Microorganisms
o System Operations
o Critical Process Parameters
o Dose Distribution
o Dosimeters
o Dose Mapping
Contract Sterilization
o Selection of the Sterilization Facility
o Obtain a Written Contract
o Verification of Validation
o Routine Processing
Prevalidation Planning
o Product and Package Materials Evaluation
o Accelerated Aging
o Establishment and Maintenance of Product Families
o Grouping into Product Families
o Selection of Family Representative
o Selection of a Sample Item Portion (SIP)
o Sterility Assurance Levels (SAL)
Microbiological Considerations
o Evaluation of Product Bioburden
o Evaluation of Bioburden Data
o Bioburden Isolates
o Product Sterility Testing
o Troubleshooting Microbiological Failures
Sterilization Support Testing
o Selection of a Test Laboratory and Test Methods
o Environmental Monitoring and Control
o Biocompatibility Testing
o Bacterial Endotoxin and Pyrogen Testing
The Validation Protocol
Outline of the Sterilization Validation
o Product and Packaging Materials Evaluation
o Equipment Qualification and Documentation
o Sterilization Dose Selection
o Dose Audit
o Dose Augmentation
o Selection of a Sterilization Dose for a Single Production Batch
o Alternate Sampling Plans for Dose Verification and Audit
Final Report
Routine Monitoring and Control
o Adopting a Device into a Validated Sterilization System
o Dose Audit Failure
o Frequency of Sterilization Dose Audits
Appendices
o Contract Radiation Sterilization Facilities in the United States
o Method 1 Dose Verification
o Method 1 Quarterly Dose Audit
o Worked Example for Method 1
o Method 2A Dose Validation
o Worked Example for Single Product Batch (SIP

Erscheint lt. Verlag 4.4.2001
Reihe/Serie Sterilization Validation and Routine Operation Handbook Series
Verlagsort Bosa Roca
Sprache englisch
Maße 216 x 279 mm
Gewicht 463 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Laboratoriumsmedizin
Naturwissenschaften Physik / Astronomie Atom- / Kern- / Molekularphysik
Recht / Steuern EU / Internationales Recht
Recht / Steuern Privatrecht / Bürgerliches Recht Medizinrecht
Technik
ISBN-10 1-58716-057-9 / 1587160579
ISBN-13 978-1-58716-057-8 / 9781587160578
Zustand Neuware
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