What does PS stand for?

Process Specification

This definition appears very rarely and is found in the following Acronym Finder categories:

Science, medicine, engineering, etc.

Other Resources:

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Samples in periodicals archive:

Hitco was selected to produce the Trailing Edge components for the B 787 Horizontal Stabilizer because of its established performance as a Gold Supplier to Boeing - particularly the C 17 and B 767 programs and its approval to Boeing's Process Specification 5578.

United Kingdom: Hitco to Supply Composite Components to Alenia for ...

In case of Web Services, we support the Business Process Execution Language (BPEL), for ebXML the tool generates choreographies according to the Business Process Specification Schema (BPSS).

Modeling eGovernment processes with UMM

that includes the specifications, production and process specifications, as well as quality assurance procedures and packaging and labeling specifications," the report noted.

Device company cited for device master record flaws and QS failures

The centerpiece of the NIST effort is the Process Specification Language (PSL), a common process language and terminology under development for manufacturing.

Predicting success. (Focus on Abrasive Machining)

According to the warning letter, Repak has changed its process specifications for its wash formula on seven separate occasions since it began production, yet the FDA could find no documentation that these changes were qualified before implementation.

Major supplier of reusable surgical drapes and gowns faulted

New Specification Aimed at Protecting Quality, Containing Cost SOLON, Ohio -- Swagelok Company unveiled a new process specification designed to meet the needs of the photovoltaic (PV) market today, aimed at helping ensure quality and reduce cost of ownership for the growing industry.

Swagelok Introduces Process Specification for Photovoltaics

The DMR does not include or refer to the location of all device and software specifications, all production and process specifications, or all installation, maintenance, and servicing procedures and methods, FDA stated.

Xoran Technologies

Also, the company was cited for failure to maintain device master records (DMR) to include or refer to the location of, device specifications, production process specifications, quality assurance procedures, and packaging and labeling specifications, and to ensure that each DMR is prepared and approved.

Avazzia cited for lack of procedures for design changes