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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...
Download now!Technical / white paper

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.
Download now!Data sheet

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
Download now!Clinical study

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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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...
Watch now!Video

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...
Watch now!On-Demand Supplier Webinar

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.
Download now!Technical / white paper

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...
Download now!Technical / white paper

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 -

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,...
Download now!Data sheet

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...
Download now!Technical / white paper

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...
Download now!Application note

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...
Download now!Application note

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...
Download now!Technical / white paper

Id Counterfeit Pharmaceuticals with Portable Raman - Rigaku

22-May-2013 - The growing danger of counterfeit and substandard medicines entering the supply chain is a concern for global pharmaceutical manufacturers and consumers. Recent innovations in instrument miniaturization enables lab-quality analysis at the point of need, providing regulatory enforcement agencies and brand...
Download now!Technical / white paper

White Paper: Is My Method Still Valid? - SGS

26-Mar-2013 - The goal of method validation is to pro­vide proof that data from each individual sample is indicative of the actual batch content with little deviation. This paper outlines the importance of validation as well as the official requirements, including characteristics...
Download now!Technical / white paper

From the Loading Dock to Quality Stock: Three Scenarios to Reduce Incoming Inspection Costs - Thermo Fisher Scientific

26-Feb-2013 - This whitepaper describes three scenarios that clearly demonstrate the value TruScan brings to pharmaceutical manufacturing facilities and the underlying benefits of implementing TruScan that make such extensive savings possible.Each case study provides an in-depth examination of the deployments of TruScan...

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