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Recently Posted Blogs
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- Analytical Discussion
AstraZeneca today announced a collaboration with the Montreal Heart Institute (MHI) in Quebec, Canada, to search the genomes of up to 80,000 patients for genes associated with cardiovascular diseases and diabetes, their complications and treatment outcomes. This is one of the largest such screens of its type to date and will drive understanding of the biological mechanisms underlying these conditions […]
F2 parameter is widely used parameter in drug dissolution testings where it is often used to predict similarity of two dissolution profiles. F2 factor In short, two profiles are considered identical when f2=100. An average difference of 10% at all measured time points results in a f2 value of 50. A public standard of f2 value between 50-100 to indicate similarity […]
The FDA cleared the Cepheid Xpert MTB/RIF Assay to help physicians determine if patients with suspected tuberculosis (TB) can be removed from airborne infection isolation. This expanded use allows healthcare providers to use one or two negative Xpert MTB/RIF Assay test results to help them determine whether a patient showing signs and symptoms of pulmonary TB should continue to be […]
Pharmaceutical Technology‘s 2015 Solid Dosage and Excipients eBook examines how advances in technology, equipment, excipients, analytical techniques, software, and manufacturing practices are facilitating the development, scale up, manufacturing, efficacy, and delivery of solid- and semi-solid dosage forms. Issue topics include: Advances in Tableting Analytical Techniques for Efficient OSD Formulation Improving Pharmaceutical Palatability Improving Efficiency in Hot Melt Extrusion and Spray […]
The new ICH Q3D Guideline for Elemental Impurities has initiated reviews and changes in quality testing programs in bio/pharmaceutical companies around the world. Companies need to assess the risks of potential elemental impurities in their process and materials streams. In this webcast, experts review the requirements of elemental impurities guidelines, practical recommendations to address implementation challenges, and key considerations for […]
Increasing requests from regulatory agencies have focused on evaluation of APIs and drug products during shipment. However, little guidance has been provided on how to address these concerns. This webinar will address these questions and explore approaches to assessing stability of biologic APIs and small molecule drug products throughout shipment. Register free: www.pharmtech.com/pt/stabilitySponsored by Patheon
This webcast invites all pharmaceutical scientists and formulators from R&D and analytical departments that have an interest in the solubilization of poorly soluble drugs, and in understanding the importance of choosing a proper dissolution method in the solubilization tests to reveal the full potential of the tested solubilization method. Register free www.pharmtech.com/dissolutionSponsored by BASF
Strategies and case studies on Systematic and Efficient Analytical Method Development for A Speedy Clinical Product Development presented by experts at Patheon. Learn how to accelerate your first-in-man studies with a deliberate approach to analytical method development for early stage drug products. Register free www.pharmtech.com/efficientSponsored by Patheon
Recently Posted Blogs
- All
- Analytical Discussion
AstraZeneca today announced a collaboration with the Montreal Heart Institute (MHI) in Quebec, Canada, to search the genomes of up to 80,000 patients for genes associated with cardiovascular diseases and diabetes, their complications and treatment outcomes. This is one of the largest such screens of its type to date and will drive understanding of the biological mechanisms underlying these conditions […]
F2 parameter is widely used parameter in drug dissolution testings where it is often used to predict similarity of two dissolution profiles. F2 factor In short, two profiles are considered identical when f2=100. An average difference of 10% at all measured time points results in a f2 value of 50. A public standard of f2 value between 50-100 to indicate similarity […]
The FDA cleared the Cepheid Xpert MTB/RIF Assay to help physicians determine if patients with suspected tuberculosis (TB) can be removed from airborne infection isolation. This expanded use allows healthcare providers to use one or two negative Xpert MTB/RIF Assay test results to help them determine whether a patient showing signs and symptoms of pulmonary TB should continue to be […]
Pharmaceutical Technology‘s 2015 Solid Dosage and Excipients eBook examines how advances in technology, equipment, excipients, analytical techniques, software, and manufacturing practices are facilitating the development, scale up, manufacturing, efficacy, and delivery of solid- and semi-solid dosage forms. Issue topics include: Advances in Tableting Analytical Techniques for Efficient OSD Formulation Improving Pharmaceutical Palatability Improving Efficiency in Hot Melt Extrusion and Spray […]
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Pharma Live wrote a new post
The benefits of this particular filling system design are courtesy of John Henry, Certified Packaging Professional (CPP), owner of consultancy Changeover.com, author of multiple packaging-related books including “Packaging Machinery Handbook” andKC Boxbottom blogger for Packaging Digest: 1. Flexibility: “Change the head and you have a whole...
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Big Data and the industrial Internet of Things can improve the operation of packaging systems, but it all starts with small data from smart sensors. Continuing developments in sensing technology have fueled user expectations in nearly every industry, and packaging...
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Sep. 28-30, 2015Las Vegas, NV PACK EXPO Las Vegas will be world’s largest packaging and processing event in 2015. The event will bring together decision makers from a wide array of industries and all across the supply chain. Combined with...
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Nerium Intl.’s updated packaging design better reflects the science behind its age-defying skincare products and creates a consistent look for its U.S. and international product lines: NeriumAD and Optimera, respectively. The sleek modern containers are white for the daytime formulas...
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new retort pouch lets food processor FasoPro package a local protein source in the African nation of Burkina Faso so the food can be delivered throughout the year to help fight devastating malnutrition among its citizens. With half its population...
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In September 2014, the union health ministry issued a notification banning the use of PET bottles for packaging of drug formulations for paediatric use, geriatric use and for use in pregnant and women of reproductive age group. The pharma...
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Nityanand Zadbuke, Sadhana Shahi, Bhushan Gulecha, Abhay Padalkar, and Mahesh ThubeAuthor information ►Article notes ►Copyright and License information ► Abstract The pharmaceutical packaging market is constantly advancing and has experienced annual growth of at least five percent per annum in the past few years. The...
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In 2006 in France, several drugs sold in poorly designed packaging exposed patients to a risk of serious adverse effects. (2) In 2006, Prescrire used a standardised methodology to examine the packaging of all new pharmaceutical products (656 different...
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Abstract Pressures from consumers, investors, insurance companies, regulators, and governments to drive down costs and improve product performance (efficacy, ease of use, patient adherence, etc.) are driving pharmaceutical companies to consider all aspects of a formulated drug, including the use...
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MeadWestvaco Corporation (MWV), a global leader in packaging and packaging solutions, announced a licensing agreement with Burgopak Ltd. MWV Healthcare will market Burgopak’s award-winning medication adherence packaging, serving the pharmaceutical and animal health markets in the United States. Patient medication...
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As Americans continue to focus on health and wellness, they are taking more control of their healthcare decisions—and they expect pharmaceutical companies to enable them even more than ever. New packaging solutions for innovative drug delivery is one of...
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Pharma Live wrote a new post
By Dr. Egon Huefner, Bürkert Fluid Control Systems When tablets are packaged in blisters, the plastic film must be the right temperature at the right moment: which is no easy task at an output of up to 1,300 blisters per...
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When it comes to meeting quality measures, manufacturers have a variety of standards from the ASTM, FDA and other organizations that they must meet. Often, these requirements include a leak testing component. Leak testing methods are recommended for everything...
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There are a few questions to ask yourself when determining which liquid filling machine is right for your project. As each machine is unique in its filling techniques and performance abilities, certain questions that are asked will help to...
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Pharma Live wrote a new post
Fastening protein-based medical treatments to nanoparticles isn’t easy. With arduous chemistry, scientists can do it. But like a doomed marriage, the fragile binding that holds them together often separates. This problem, which has limited how doctors can use proteins...
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