OC in Fda Meaning
The OC meaning in Fda terms is "Quality Control". There are 5 related meanings of the OC Fda abbreviation.
OC on Fda Full Forms
- Quality Control Quality control is a procedure or set of procedures intended to ensure that a manufactured product or performed service adheres to a defined set of quality criteria or meets the requirements of the client or customer. QC is similar to, but not identical with, quality assurance (QA). QA is defined as a procedure or set of procedures intended to ensure that a product or service under development (before work is complete, as opposed to afterwards) meets specified requirements. QA is sometimes expressed together with QC as a single expression, quality assurance and control (QA/QC). The operational techniques and activities that are used to fulfill requirements of quality.
- Immediate Office of The Commissioner (oc)
- Office of Compliance
- Office of The Commissioner (fda)
- Immediate Office of the Commissioner
Frequently Asked Questions (FAQ)
What does OC stand for Fda?
OC stands for Immediate Office of The Commissioner (oc) in Fda terms.
What is the shortened form of Quality Control in Fda?
The short form of "Quality Control" is OC for Fda.
Citation
OC in Fda. Acronym24.com. (2022, March 27). Retrieved May 15, 2024 from https://acronym24.com/oc-meaning-in-fda/
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