Quality Control (QC) and Quality Assurance (QA) are fundamental in ensuring the safety, efficacy, and consistency of pharmaceutical products. QC focuses on the testing and inspection of raw materials, in-process components, and finished products to confirm they meet specified standards. Rigorous testing methods, including stability studies and bioavailability assessments, are integral to QC practices. On the other hand, QA ensures that the entire manufacturing process adheres to predefined standards and regulations, preventing defects and maintaining quality across production cycles. By implementing robust QA systems, pharmaceutical companies ensure that drug formulations are developed and delivered according to regulatory guidelines. Both QC and QA work in tandem to uphold product integrity, streamline production processes, and safeguard patient health, making them indispensable in the pharmaceutical industry's commitment to delivering safe, reliable, and effective therapies.
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