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Amino Acid Analysis According to Ph.Eur 2.2.56 - SGS

23-Feb-2015 - Employing spectrophotometry and liquid chromatography quantitation of Ninhydrin-positive substances achieves 0.05% reporting sensitivity as required by the updated Ph.Eur 2.2.56. This white paper details our results compliant with the new monographs
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A Method to Meet the New Ph Eur Ninhydrin-Positive Substances Requirement - Butterworth

03-Feb-2015 - The European Pharmacopeia (Ph Eur) is moving away from the historical thin layer chromatography technique for the determination of Ninhydrin-positive substances, to more specific and sensitive methods utilising Liquid Chromatography (LC) or Amino Acid Analysers. This paper will explore the...
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Enabling Taste Masking with Lipid Multiparticulate and Osmotic Bursting Technology - Capsugel

08-Jan-2015 - Taste is an important parameter governing compliance with oral dosage forms, affecting a variety of patient cohorts. Many active ingredients have bitter taste; hence effective taste masking via smart formulation design can translate into improved compliance and overall therapeutic value for patients. This...
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USP<233> Elemental Impurities Sample Prep Strategy - SGS Life Science Services

03-Nov-2014 - Although USP <232> and <233> are still under discussion, a good deal of work is going on ahead of implementation in terms of method development. High on the list is developing and validating methods for sample preparation. Learn more in...
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A brief history of bioavailability - William Reed Business Media

30-Sep-2014 - Tablets have been around for almost 200 years. In this presentation we trace the history of their development, from the accidental invention of the sustained release pill through to the latest breakthroughs in bioavailability enhancement, this talk will take us...
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Bioavailability market dynamics - William Reed Business Media

23-Sep-2014 - How healthy is demand for bioavailability enhancement services? Is the growth of the generics sector driving the market or do innovative pharma firms determine the type of solubility solutions that are available.When biopharmaceutical are injected they are 100% bioavailable, but...
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Comparison Trials on Herbal Extract Syrups Based on LYCASIN® 80/55 and Simple Sucrose - Roquette

01-Sep-2014 - Formulating a sugar-free syrup being at the same time stable and with a pleasant taste can be a real challenge. LYCASIN®, a liquid maltitol with a sweet and pleasant taste, is one of the most suitable sugar replacement solutions in...
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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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