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Quality Control (QC) and Quality Assurance (QA)

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.

Committee Members
Speaker at Pharmaceutical Conference - Consolato M Sergi

Consolato M Sergi

Universities of Alberta and Ottawa, Canada
Speaker at Drug Delivery Events - Vladlen Slepak

Vladlen Slepak

University of Miami Miller School of Medicine, United States
Speaker at Drug Delivery Events -  Andreas M Papas

Andreas M Papas

Antares Health Products, United States
Speaker at Drug Delivery Events - Sergey Suchkov

Sergey Suchkov

The Russian University of Medicine and Russian Academy of Natural Science-Moscow, Russian Federation
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