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Stability Analysis

The capacity of drug formulations to preserve physical, chemical, biological, and microbiological stability is referred to as its Stability. A detailed investigation of medication stability is critical in quality management and ensuring medicinal effectiveness. The fundamental needs of pharmaceuticals are safety, effectiveness, and stability. Drug Stability implies that a drug substance should have the same features and characteristics as it had at the time of manufacture and during the time range provided. The stability of pharmacological preparations has a direct impact on therapeutic efficacy and safety. As a result, it is critical to investigate the stability of pharmaceutical formulations in order to assure the quality of the product, safety, and efficacy. All drug research and manufacture is based on Stability Analysis. To guarantee that stable items meet all regulatory criteria before entering markets, all organisations must have a clear vision for the appropriate stage of stability research design. All businesses must have a clear vision for the right stage of stability research design in order to ensure that stable goods fulfil all regulatory standards before accessing markets.

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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