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Schreiner MediPharm
Schreiner MediPharm
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Packaging
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Trending Articles
Innovation in generics: increased efficiency through peptide API synthesis expertise
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AstraZeneca's INFORM study highlights the persistent danger of COVID-19 for the immunocompromised despite the vaccination scheme
US court lifts modified consent decree on Xellia’s Cleveland facility
The Modified Consent Decree imposed on Xellia's Cleveland facility in 2016 has been vacated, receiving a VAI
Lonza's AI-enabled small molecule development tool launches
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Autoscribe Informatics’ new Australia office supports business growth
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Upcoming event
ASGCT Annual Meeting 2024
7-11 May, 2024 | Meeting | Portland, OR
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Related Content
Packaging
Schreiner Group establishes Jinshan site
The expansion allows the company to enhance its global competitiveness
Manufacturing
Schreiner MediPharm presents new sustainable closure seals
Schreiner MediPharm, a leading expert in pharmaceutical packaging solutions, successfully kicked off the 2024 trade fair year at Pharmapack in Paris from January 24-25
Manufacturing
Schreiner MediPharm Enables Digital Adherence Monitoring with New Child-Resistant Smart Blister Wallet
The company also ensures end-to-end automated production of the Smart Blister Package due to scalable state-of-the-art manufacturing processes
Packaging
Needle-Trap offers new first-opening indication feature
Due to its integrated plastic trap, the Needle-Trap needle protection label poses special challenges to a first-opening indication feature
Packaging
Premiere at PDA: Prefilled Syringes with RFID-Labels
The partnership between Schreiner MediPharm and SCHOTT Pharma has previously been focused primarily on equipping COC syringes with analog functional labels
Packaging
Schreiner MediPharm launches tamper evidence protection label
Drug counterfeiters frequently fill original pharmaceutical containers with ineffective or harmful substitutes
Regulatory
Schreiner and Aardex offer product combination for trial adherence
The product combination is designed to enhance compliance with the requirements and dosing regimens of the clinical trial protocols proposed by the FDA and the European Medicines Agency
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