- General Principles of Process Validation
- Фармация: общие принципы валидации
Универсальный англо-русский словарь. Академик.ру. 2011.
General Principles of Process Validation
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Validation (drug manufacture) — Within the highly regulated environment for development and manufacturing of Pharmaceutical Drugs and medical devices there is a requirement within the regulations to provide an appropriate amount of assurance that critical processes in producing … Wikipedia
Verification and validation — IV V redirects here. For NASA s IV V Facility, see Independent Verification and Validation Facility. Verification and validation is the process of checking that a product, service, or system meets specifications and that it fulfills its intended… … Wikipedia
Verification and Validation — Verification Validation is the process of checking that a product, service, or system meets specifications and that it fulfils its intended purpose. These are critical components of a quality management system such as ISO… … Wikipedia
Business process management — (BPM) is a method of efficiently aligning an organization with the wants and needs of clients. It is a holistic management approach that promotes business effectiveness and efficiency while striving for innovation, flexibility and integration… … Wikipedia
Computerized system validation — Computer system validation (CSV) is the documented process of assuring that a computer system does exactly what it is designed to do in a consistent and reproducible manner. The validation process begins with the system proposal/requirements… … Wikipedia
General relativity — For a generally accessible and less technical introduction to the topic, see Introduction to general relativity. General relativity Introduction Mathematical formulation Resources … Wikipedia
Data Validation and Reconciliation — Industrial process data validation and reconciliation or short data validation and reconciliation (DVR) is a technology which is using process information and mathematical methods in order to automatically correct measurements in industrial… … Wikipedia
Business process reengineering — (BPR) is a management approach aiming at improvements by means of elevating efficiency and effectiveness of the processes that exist within and across organizations. The key to BPR is for organizations to look at their business processes from a… … Wikipedia
Information technology audit process — Information technology audit process:Generally Accepted Auditing Standards (GAAS)In 1947, the American Institute of Certified Public Accountants (AICPA) adopted GAAS to establish standards for audits. The standards cover the following three… … Wikipedia
Validierung (Pharmatechnik) — Durch die Validierung wird der dokumentierte Beweis erbracht, dass ein Prozess oder ein System die vorher spezifizierten Anforderungen (Akzeptanzkriterien) reproduzierbar im praktischen Einsatz erfüllt. Die US amerikanische Behörde für… … Deutsch Wikipedia
Automated Tissue Image Systems — (ATIS) are computer controlled automatic test equipment (ATE) systems classified as medical device and used as pathology laboratory tools (tissue based cancer diagnostics) to characterize a stained tissue sample embedded on a bar coded glass… … Wikipedia
