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Stability data Requirements for a Marketing Authorization Application

Stability data Requirements for a Marketing Authorization Application

Any drug substance or drug product has to maintain the same quality, safety and efficacy throughout the lifecycle of a product. Generally, the quality of a drug substance or drug product varies with time under the influence of a variety of environmental factors such as temperature, humidity, and light. As we understood the quality of substance or product is varying in the presence of temperature and humidity over the period of time, any sponsor/applicant needs to provide supporting data and...

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Residual Solvents – Basics, Classification and Assessment

Solvent – A substance, majorly liquid capable of dissolving or diluting other substances to form a solution.  Generally, several solvents are used in the manufacturing of drug substance, excipients and drug products as a routine practice. The solvents are used to enhance the solubility, yield and to determine several critical factors needed for the final product, considered as a critical element in the manufacturing process. The solvents are organic and volatile in nature that are...

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Impurities – Classification, Thresholds Limits, Specification with RTR Considerations in APIs and Finished Products

Impurities – Classification, Thresholds Limits, Specification with RTR Considerations in APIs and Finished Products

Every product should have a sufficient level of quality to ensure its efficacy and safety. The impurities/degradation products are the ones that arise during different stages of synthesis, manufacture and storage. They should be controlled at certain level to maintain the required quality of the drug substance/product. The potential impurities are most likely to arise during the synthesis of drug substance, purification, manufacturing and storage of the drug substance/drug product. The...

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FDA Novel Drug Approvals in January 2022

QUVIVIQ ITEMDESCRIPTIONSPONSOR/HOLDERIDORSIA PHARMACEUTICALS LTDApplication No.#214985Application TypeNDAActive IngredientDaridorexantDosage FormTABLETRoute of AdministrationORALStrengthsEQ 25mg BaseIndication for UseTreatment of adult patients with insomnia, characterized by difficulties with sleep onset and/or sleep maintenanceApproval Date07/01/2022 CIBINQO ITEMDESCRIPTIONSPONSOR/HOLDERPFIZER INCApplication No.#213871Application TypeNDAActive IngredientAbrocitinibDosage FormTABLETRoute of...

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FDA Novel Drug Approvals in January 2023

The U.S Food and Drug Administration (USFDA) has approved 04 new drugs in the month of January. Out of the 04 approvals, 03 are NDA and 01 is BLA. LEQEMBI ITEMDESCRIPTIONNDA/BLA Number:761269Applicant/Holder:EISAI INCAPI:LecanemabDosage Form:INJECTABLE/INJECTIONStrengths:500MG/5ML; 200MG/2MLIndications:Indicated for the treatment of Alzheimer’s diseaseApproval Date:06/01/2023 BRENZAVVY ITEMDESCRIPTIONNDA/BLA Number214373Applicant/HolderTHERAXOSBIO LLCAPIBexagliflozinDosage...

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