Video
23 Nov 2021
Effective Solubilization & Bioavailability Enhancement of Poorly Water Soluble APIs
Content provided by our supplier
Clariant
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CH
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2015On CPHI since
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2Certificates
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5000+Employees
Company types
Other Content from Clariant (2)
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Video Reimaging Chemistry to Improve Medicines: High Functional Excipients to increase APIs effectiveness
In today’s world, medical innovations and pharmaceutical technology are essential drivers of human health: they open up the possibility of new treatments and subsequently act as a gateway which allows people around the world to access new medicines, improving their quality of life.
In the production of pharmaceuticals, high-quality ingredients play a crucial role and must meet ever-increasing expectations in quality assurance to guarantee that safe, effective medicines reach the end consumer.
Clariant Health Care is a leading high-quality solution partner for the global pharmaceutical industry, with a strong portfolio of top-performing excipients and active pharmaceutical ingredients (APIs), backed by operational excellence and years of experience in regulatory affairs.
Explore Clariant’s high functional excipients to enable APIs bioavailability enhancement, controlled release, target delivery, stabilization, continuous manufacturing, preservation and viscosity enhancement.
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Video Widely Used Solvent with Stringent Control of Microbial Load
This session was originally broadcast as part of the CPHI Worldwide 2021 digital content programme. Low molecular weight Polyethylene glycols 300 & 400 are commonly used in formulations as solvents for APIs which are not soluble in water. For high-risk applications, stringent control of microbial load is essential. VitiPure™ LEX 300 and VitiPure™ LEX 400 offer relevant product specifications making them suitable for high-risk applications. This session explores: Low molecular weight PEG 300 (VitiPure™ LEX 300) and PEG 400 (VitiPure™ LEX 400) with Low microbial load for high-risk applications Surpass the current pharmacopoeia requirements Microbiological specifications support risk assessment in pharmaceutical and biopharmaceutical manufacturing
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