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2. Work method statement - Wikipedia

   en.wikipedia.org/wiki/Work_method_statement

   A work method statement, sometimes referred to as a safe work method statement or SWMS or a safe work procedure, is a part of a workplace safety plan. [1] It is primarily used in construction to describe a document that gives specific instructions on how to safely perform a work related task, or operate a piece of plant or equipment.

3. Operations manual - Wikipedia

   en.wikipedia.org/wiki/Operations_manual

   The operations manual can be a digital or paper document. Digital format has advantages for revision control and can be distributed easily and at low cost. [4] The detail should be sufficient to allow a competent person without specific experience to understand what is needed and how it is to be done.

4. Manufacturing process management - Wikipedia

   en.wikipedia.org/wiki/Manufacturing_process...

   Manufacturing process management (MPM) is a collection of technologies and methods used to define how products are to be manufactured. MPM differs from ERP/MRP which is used to plan the ordering of materials and other resources, set manufacturing schedules, and compile cost data.

5. Standard operating procedure - Wikipedia

   en.wikipedia.org/wiki/Standard_operating_procedure

   A standard operating procedure (SOP) is a set of step-by-step instructions compiled by an organization to help workers carry out routine operations. [1] SOPs aim to achieve efficiency, quality output, and uniformity of performance, while reducing miscommunication and failure to comply with industry regulations.

6. Shop drawing - Wikipedia

   en.wikipedia.org/wiki/Shop_drawing

   Some fabricators and manufacturers will provide symbols, data, or instructions concerning installation. This can include a list of other materials, such as fasteners or adhesives, appropriate but not included for the product. Third party review may be required for major building systems.

7. Good manufacturing practice - Wikipedia

   en.wikipedia.org/wiki/Good_manufacturing_practice

   Manufacturing processes must be controlled, and any changes to the process must be evaluated. Changes that affect the quality of the drug are validated as necessary. Instructions and procedures must be written in clear and unambiguous language using good documentation practices. Operators must be trained to carry out and document procedures.