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Seminar on : Validation of Sterilization Process Date : Nov 26 or 27, 2008 (Wednesday & Thursday) Time : 6 :30 pm 8:30 pm (Light Refreshment Provided) Venue : Lecture Theater, M/F, Hospital Authority
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Professionals working in industries where validation is crucial, such as pharmaceuticals, medical devices, food production, or manufacturing.
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Seminar on validation of is a process to ensure that a product, system, or process meets the requirements and specifications set by regulatory authorities or internal standards.
Companies or individuals involved in the development, manufacturing, or distribution of products or services that are subject to regulatory requirements.
Seminar on validation of can be filled out by providing relevant information about the validation activities performed, results obtained, and any deviations or corrective actions taken.
The purpose of seminar on validation of is to demonstrate that a product, system, or process is fit for its intended use, meets regulatory requirements, and produces consistent and reliable results.
Information such as validation protocols, test results, acceptance criteria, deviations, corrective actions, and verification of compliance with regulatory requirements.
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