validation refers to establishing documented evidence that a process or system, when operated within established parameters, can perform effectively and reproducibly to produce a medicinal product meeting its pre-determined specifications and quality attributes
Monday, January 1, 2018
Understanding Steam Sterilization
Meeting the parameters of time, temperature and steam under pressure, steam sterilization is the most effective and efficient sterilization method in dentistry. Understand how to maintain your sterilizer; use the appropriate accessories; record sterilization parameters and what to look for during the ideal sterilization cycle. Don't Risk It! Direct questions to 1-8558-STERILE (Toll-Free) 8am-5pm M-F MST. Crosstex International, Inc. Video Disclaimer This video is owned by the sole property of Crosstex International, Inc. ("Crosstex") and is to be used solely for internal informational purposes. Any copying, distribution, posting or editing of this video production in any format, or any unauthorized or improper use of this video, is strictly forbidden. The information presented in this video is based on current information at the time of production. Crosstex makes no warranty or guarantee concerning the accuracy or reliability of the content of this video. For technical and regulatory guidance, please refer to applicable instructions for use and product labels with respect to any product or process described in this video and current official versions of applicable state, federal or other governmental or regulatory rules, laws, standards, policies, protocols and recommended best practices. Content is subject to change at any time. ©2014 Crosstex International, Inc. All rights reserved.
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Pharmaceutical Validation Documentation Requirements
Pharmaceutical validation is a critical process that ensures that pharmaceutical products meet the desired quality standards and are safe fo...
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K. Dashora, D. Singh, Swarnlata Saraf and S. Saraf *. Institute of Pharmacy, Pt.RavishankarShuklaUniversity, Raipur 492 010. *Author for ...
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Validation of the Autoclave is classified into the following 1.0 OQ – Operational Qualification 2.0 PQ – Performance Qualification The valid...
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Cold storage is a relatively simple cold room that is commonly used to store material between 2[degrees] to 8[degrees]C. Such cold rooms a...
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