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Technology Selection To Enhance Oral Bioavailability - Capsugel

20-Aug-2014 - Effective technology selection for improving bioavailability (BA) can accelerate the development of promising compounds and reduce the overall cost and complexity of drug development. Science-based technology selection requires an understanding of the scientific fundamentals governing drug solubilization, absorption and metabolic...
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Optimizing API Stability Through Purity - Croda

21-Jul-2014 - It is crucial to optimize your drug active’s environment to ensure the stability of the API.  A high purity excipient can help by minimizing the occurrence of impurities that could accelerate drug active degradation.  Offering the most highly-purified excipients available,...
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Determination of moisture in a protein sample using a portable NIR instrument - Thermo Fisher Scientific

03-Jun-2014 - Near infrared spectroscopy has been used effectively to measure moisture in a wide variety of samples. Due to the large overtone band for water in NIR, levels of accuracy tend to be high and limits of detection are lower than...
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Do you have spores? - Steris

27-May-2014 - Trending analysis of cleanroom environmental monitoring data sometimes shows the presence of spores. These undesirable microbes must be eradicated quickly to reduce the risk to the product being manufactured. When spore formers like the highly resistant “bacillus Cereus or subtilis”...
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Excipients for Multilayer Tablets - JRS PHARMA LP

07-May-2014 - Multi-layered tablets bring together differently formulated powder mixtures, which typically contain different APIs, into a single tablet with two or more layers. They offer benefits for overcoming API-API interactions and stability issues, tailoring dissolution profiles, and bringing brand recognition to...
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Elemental Impurity Analysis in Pharmaceuticals - Butterworth

06-May-2014 - A method to identify the presence of heavy metals in pharmaceuticals was introduced in the United States Pharmacopoeia more than 100 years ago. Today pharmaceutical companies are still using essentially the same method, the USP <231> Heavy Metals Limit Test....
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Near-infrared spectroscopy - Metrohm – customized analysis for the pharmaceutical industry

01-May-2014 - NIRSystems Technology:  Improved productivity and faster quality control of starting materials, intermediates and final products. Learn more
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CREMER OLEO has become the holder of the first CEP ever granted for a Medium-Chain Triglyceride (MIGLYOL® 812 N). - CREMER OLEO GmbH & Co. KG

28-Apr-2014 - CREMER OLEO has gathered its activities for the pharmaceutical industry under the roof of CREMER Health, with a strong commitment to quality leadership in Oleoceuticals. Our pharmaceutical excipients for topical, oral and rectal applications as well as our oleo-chemical based active...
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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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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...
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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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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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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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