Cornell researchers reveal that an existing FDA-approved drug can facilitate the delivery of other large molecules across the blood-brain barrier. / read more /
Pharmaceutical Technology and BioPharm International are sponsoring Keynote Series discussions at INTERPHEX 2016 on addressing sterile manufacturing challenges. Experts involved in this work discuss recent initiatives, and offer insights into what must be done to prevent injectables shortages in the future.
The IMS Institute for Healthcare Informatics report examines spending on medicine in the US, drivers of growth, major market segments, prescription volume, patient costs, and healthcare delivery changes. / read more /
Transferring the manufacturing of a drug from one scale to another or between manufacturing sites presents both technical and business challenges.. / read more /
The authors discuss the concept design of a versatile, sustainable, small-scale facility in Malta that conforms to the European Union's current good manufacturing practices. / read more /
Pharmaceutical Technology spoke with FDA to get the agency’s insights on how the industry can ensure quality in solid and semi-solid dosage products. / read more /
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The Top 4 Most Expensive Encapsulation Mistakes and How to Avoid Them LIVE WEBCAST: Thursday, April 21, 2016 at 9 am EDT | 3 pm CEST Free registration
Innovative Softgel Solutions to Enhance Bioavailability and Patient Experience
Catalent has over 80 years of softgel manufacturing experience, and continues to deliver innovation with technological enhancements, such as chewable softgels and coatings, and formulations to enable modified-release for Rx, OTC and consumer health products.
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We are manufacturers of laboratory reagents and fine chemicals for industrial use. Our products are marketed worldwide through an extensive distribution network to more than 80 countries, under the brand PanReac AppliChem.
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Ensuring Effective Drug Stability Studies Drug Stability Testing from Development to Shipping LIVE WEBCAST: US: Wednesday, April 20, 2016 at 11 am EDT and EU: Wednesday, April 27, 2016 at 11 am CEST In this educational webcast, learn about regulatory expectations and practical approaches to stability testing of drug substances and drug products for clinical trials, packaging, storage, and transportation. Free registration
KEYNOTE SERIES AT INTERPHEX 2016
At INTERPHEX 2016, Pharmaceutical Technology and BioPharm International are sponsoring a Keynote Series addressing leading bio/pharma industry issues.
In a panel discussion, Industry experts will discuss how technology advances are addressing challenges in biopharmaceutical development including quality control of raw materials, implementation of single-use technologies, process monitoring, and downstream purification.
Tuesday, April 26, 10:15 am to 11:45 am Learn more
How will consolidation in the bio/pharmaceutical and contract services market, a changing financial market, and an active political and regulatory year shape the fortunes of the contract services market? In his annual presentation, industry expert Jim Miller will offer his perspectives on the contract services landscape for the next few years.
Wednesday, April 27, 10:30 am – 11:30 am Learn more
Employing a Lean Lab Approach to Optimize Lab Processes: Part 1: Work Smarter Not Harder LIVE WEBCAST: Tuesday April 26, 2016 at 7 am PDT | 10 am EDT | 2 pm GMT | 3 pm BST | 4 pm CET When lab workloads seem too high to handle, analysis results or approvals are late, or lead times are exceeded, it is time to take a closer look at a lean lab approach, especially before investing in new resources such as equipment, premises, or personnel. Free registration
Learn about adaptive clinical trials, patient recruitment strategies, and advanced biomarker analysis tools designed that can accelerate drug development and clinical testing processes. Sponsored by SGS
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Join our free webinar for a case study on the handling of complex manufacturing expansion projects, with insight on simulation and visualization tools, innovations for manufacturing of parenterals, effective team building, and more. Sponsored by Baxter
A compilation of informative, useful articles designed to help you meet the challenges of process analytical technology, be more efficient in testing, reduce over-processing, enhance consistency, and minimize rejects. / Click here /
New materials, instruments, and processes are facilitating solid-dosage drug formulation and manufacturing. This ebook reviews methods to address quality issues for APIs, excipients, and intermediates; analysis methods for elemental impurities and continuous powder processing; modeling tools to improve workflows, and methods to improve tablet compression.
