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APIs (active pharmaceutical ingredients)

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How glass-forming polymers improve bioavailability / Enhanced oral bioavailability with Soluplus® – case study - BASF SE

26-Mar-2014 - How glass-forming polymers improve bioavailabilityPolymers are essential components of oral solid dosage forms and used as binders, disintegrants or coatings. Given the increase in poorly water-soluble drugs, not only well-known but also specifically designed polymers (e.g. Soluplus®) can be used...
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Want to Strengthen Your Supply Chain Security? -

18-Mar-2014 - The challenges of ensuring safe drugs for patients are universal, international and pervasive. The Global Forum on Access to Safe Medicines brings together a host of global leaders dedicated to improving supply chain security and preventing falsified, counterfeit, diverted and...
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Dow AFFINISOL™ polymers for Solubility Enhancement - Dow Pharma & Food Solutions

12-Mar-2014 - Dow’s AFFINISOL™ line of excipients include AFFINISOL™ HMPCAS for spray drying applications and AFFINISOL™ HPMC for hot melt extrusion (HME) applications. Hypromellose acetate succinate (HPMCAS) has proven effective at producing stable amorphous solid dispersions for poorly soluble APIs. We will highlight: •...
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Role of excipients in design of solid amorphous drug dispersions for delivery of poorly water-soluble drugs - Ashland

10-Mar-2014 - Most new drug candidates suffer from poor water- solubility leading to rate limiting dissolution, slow absorption and limited bioavailability. Solid amorphous drug dispersions are most commonly used improve bioavailability by enhancing drug solubility. The selection of the right solid dispersion...
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Method Validation for Heavy Metals Testing - SGS

04-Mar-2014 - USP proposed <232> and <233> changes require ICP and ICP-MS instrumentation and methodology expertise, and knowledge of sample preparation. Also strategies to overcome sample interferences and achieve acceptable elemental recovery criteria are key.
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Enhancing Actives Delivery for Optimal Formulation Efficacy - Croda

24-Feb-2014 - Excipients designed to enhance skin penetration can maximize the efficacy of topical formulations.  Through lipid disruption and skin polarity modification, topical penetration enhancers allow for more targeted API delivery.  Fill out the form for more information
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Bioavailability Enhancement Series: Hot-Melt Extrusion - Capsugel

18-Feb-2014 - Hot-melt extrusion (HME) of amorphous solid dispersions is one approach Bend Research uses to address APIs with limited bioavailability due to low solubility and dissolution rates (DCS IIa and IIb). Please join us to discuss solid dispersion formulation selection and...
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Solving your sticking problems with Tabletting Science - I Holland Limited

09-Jan-2014 - This webinar looks at why tablet formulations stick to punch tip faces and how to overcome sticking using punch coatings. We will highlight to tablet manufacturers how quickly a solution can be recommended using I Holland's new TSAR model.
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The Probiotics category has grown by 250% - Cell Biotech Europe A/S

19-Feb-2014 - Do you want a big-selling probiotic product portfolio?A recent published study proves a 68% effect in 4 weeks on alleviating irritable bowel syndrome symptoms by using patented double-coated probiotics from the worlds leading probiotic manufacturer. The unique, patented double-coating from...
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Enhanced Crystallisation Control Improves Polymorph Screening - Genevac

20-Jan-2014 - Genevac announces eXalt - an exciting new non-destructive technology that enables a wide range of solvents and multiple actives to be evaporated all at the same slow rate, and under the same conditions, giving the user unprecedented control of crystallisation...
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Key to Outsourcing Method Development and Validation: A Pragmatic Approach -

12-Dec-2013 - In an industry that is seeing an increasing level of work being outsourced, alongside a focus for companies to achieve ever shorter timelines to get a new drug to market; it is vital that a tailored, pragmatic approach is adopted...
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Embedding Q and R Practice in Pharma Ingredient Manufacture - Corbion Purac

09-Dec-2013 - A growing amount of Q&R applies to creating pharmaceuticals. Pharmaceutical manufacturers prefer ingredients developed with compliance that exceeds legal requirements. As the Q&R landscape evolves and its complexity deepens, it becomes increasingly challenging for pharmaceutical ingredient manufacturers to achieve a...
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A One Stop Shop Solution For manufacture of ADC's - Fujifilm

26-Nov-2013 - ADCs are showing great promise as a new therapeutic entity, but have a complex supply chain requiring biologics and high potency capability. This presentation from Piramal and Fujifilm Diosynth will demonstrate our integrated approach for rapid delivery of ADCs.
Download now!Technical / white paper

NEOBEE® MCTs Enhance Pharmaceutical Bioavailability - Stepan Lipid Nutrition

04-Nov-2013 - An efficient solvent for many lipophylic drugs and vitamins, NEOBEE® MCTs emulsify in aqueous environments and help uptake in intestinal cells. They are odorless, tasteless and extremely stable and offer a safe, versatile, affordable and simple solution for many bioavailability...
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New Guidelines for Stabilization of Proteins by Freeze Drying: Formulation and Process Heresy - Baxter

17-Oct-2013 - Over the years a number of informal guidelines or “rules” for the formulation and processing of proteins for freeze-drying have been developed. However, in recent years it has become obvious that some of these rules need modification. In this presentation,...
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Improving API Stability with Increased Excipient Purity - Croda

14-Oct-2013 - Sensitive or unstable APIs can pose formulating challenges when it comes to ensuring their consistent and safe delivery.  Data indicate that the purity level of an excipient can have a notable influence on the stability of pharmaceutical actives.
Download now!Technical / white paper

CONFIDENCE IN BIOLOGICS FORMULATION DESIGN - SGS Life Science Services

07-Oct-2013 - To ensure a long product shelf-life for biopharmaceutical drug products, a stable storage environment is critical. Determination of the optimal environment is initiated early in the development process through preformulation screening. In order to maintain potency and activity of protein...
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Analysis of Biopharmaceuticals to Conform to ICHQ6B -

25-Sep-2013 - Biopharmaceuticals - incorporating originator, biosimilar and biobetters molecules - are expected to grow to a $1 billion market sector by 2017.  The quality and testing regimes that must be applied to the molecules during development, submittal to the regulatory authorities...
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Cell Culture Media Identification with Handheld 1064 Nanometer Raman - Rigaku

23-Sep-2013 - Biopharmaceutical production is a rapidly growing and high risk industry. According to a market research report, only three of ten drugs receive market clearance. Cell culture media plays an important role in biopharmaceutical production. Handheld Raman provides the means for...
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Handheld 1064nm Raman boosts excipient analysis capacity - Rigaku

21-Aug-2013 - Pharmaceutical manufacturers the world over seek more efficient technologies for materials validation. Implementation of handheld Raman spectrometers utilising a 785nm wavelength laser  revealed a limitation in the technology’s ability to identify many common materials, often excipients. Instrument miniaturization advancements resulted...

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