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FDA Approves Immunoglobulin Formulation With Low IgA Content for Primary Immunodeficiency

Pharmacy Times

Takeda will discontinue Gammagard S/D by December 2027, transitioning to the new low IgA formulation. Takeda has informed the FDA that the manufacturing of Gammagard S/D will cease in December 2027.

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17th edition of CPHI & PMEC India inaugurated at India Expo Centre, Noida

Express Pharma

Spanning pharma machinery, packaging, analytical instruments, laboratory technologies, ingredients, and beyond, it offers a comprehensive platform for stakeholders to engage in transformative dialogues and foster strategic partnerships. With exports nearing $27.84 Adam Anderson , Executive VP – Pharma, Informa Markets B.V

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Moving towards oral delivery of biologics

European Pharmaceutical Review

1 Used to treat a range of chronic diseases (eg, diabetes, rheumatoid arthritis, psoriasis, Crohn’s disease, haemophilia, etc), it is projected that the sales of biologics will rise from $380 billion in 2022 to $416 billion in 2023, and to almost $600 billion in 2027. the enteric coating and the capsule dissolve.

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Injectable Drug Delivery 2022

pharmaphorum

reaching £915 billion by 2027. Delve into the world of biologics and biosimilars and what these mean for the injectable drug market. The injectable drug delivery market is expected to rise at a compound annual growth rate of 12.9% Develop your understanding of high-volume and long-acting injectable compounds. Device Engineering.

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State-Led Food Transparency: Texas and Louisiana Lead the Charge

FDA Law Blog: Biosimilars

Texas Goes BIG on Food Warnings Beginning on January 1, 2027, Texans may notice new warning labels on some food products sold in their fair state. This labeling requirement will apply to packages “developed or copyrighted” from January 1, 2027 onward. Here’s what industry needs to know. Preservatives such as BHA and BHT.