Home » Fda » What does QC mean in Fda?

QC in Fda Meaning

The QC meaning in Fda terms is "Quality Control". There are 1 related meanings of the QC Fda abbreviation.

QC on Fda Full Forms

  1. 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.

Frequently Asked Questions (FAQ)

  1. What does QC stand for Fda?

    QC stands for Quality Control in Fda terms.

  2. What is the shortened form of Quality Control in Fda?

    The short form of "Quality Control" is QC for Fda.

Citation

QC in Fda. Acronym24.com. (2021, December 15). Retrieved November 25, 2024 from https://acronym24.com/qc-meaning-in-fda/

Last updated