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Pharmaceutical Testing

Pharmaceutical testing is a fundamental process in ensuring the safety, efficacy, and quality of pharmaceutical products. It involves a thorough examination of drugs and medicinal substances at different stages of development and production. Stringent testing protocols are in place to meet regulatory standards, ensuring that pharmaceuticals adhere to the highest quality benchmarks.

Analytical testing is a cornerstone of pharmaceutical testing, employing techniques such as chromatography, spectroscopy, and mass spectrometry to evaluate the composition and purity of drug formulations. Stability testing is equally vital, investigating how pharmaceutical products react under diverse conditions over time to ascertain their shelf-life and efficacy.

Quality control measures encompass microbiological testing, where products undergo assessment for the presence of microorganisms that could pose safety risks. Bioavailability and bioequivalence studies play a key role in understanding how the human body absorbs and processes pharmaceuticals.

Pharmaceutical testing is a dynamic field that adapts to emerging technologies and regulatory requirements. Its ongoing evolution is crucial in upholding the integrity and effectiveness of pharmaceutical products, ultimately safeguarding public health.

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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