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QbD in API Manufacturing
With a quality-by-design approach, robust processes consistently can help deliver quality product.

Exploring Newly Introduced Methods for Testing MDIs with Add-On Devices
The role of add-on devices and how they affect drug delivery with a pressurized metered dose inhaler.

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Data Integrity Key to GMP Compliance
FDA demands accurate manufacturing and test information to ensure product quality.

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Thomson Reuters Projects Pharma Sales Will Reach $1 Trillion in 2014
The Reuters Annual Pharmaceutical Factbook reveals positive outlook for pharmaceutical industry and key insights into current trends.

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Nisso low viscosity HPC for dry binding
Special low viscosity, super fine powder grade Nisso HPC-SSL-SFP is a new dry binder for direct compression, ODT, roller compaction, extra-granule addition applications. Excellent tablet hardness and friability properties can be achieved in dry binding applications using 3% or less of binder and with minimal-to-no impact on disintegration times and dissolution profiles. Learn more |
FDA Approves XTANDI Capsules for Prostate Cancer
FDA approved XTANDI for the treatment of metastatic castration-resistant prostate cancer.

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API Characterization for a Speedy and Successful Formulation Strategy
September 18, 2014 at 11:00 AM EDT
To Register Free: www.pharmtech.com/strategy |
Generic Pharmaceutical Association Reports Record Cost Savings
A GPhA report says generic drugs saved the US health system $239 billion in 2013.

FDA Approves Treatment for Children with Hemophilia B
FDA approved Baxter International's treatment, RIXUBIS, for the treatment of children with hemophilia B.

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Systematic and Efficient Analytical Method Development for A Speedy Clinical Product Development
October 15, 2014 at 11:00 AM EDT
To Register Free: www.pharmtech.com/Efficient |
EYLEA Receives FDA Breakthrough Therapy Designation
Regeneron Pharmaceuticals' injection for diabetic retinopathy in patients with diabetic macular edema received FDA breakthrough therapy designation on Sept. 16, 2014.

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The Global Quality Workflow: Making the Transition from Manual to Automated Compliance Processes
Tuesday, September 30, 2014 at 11:00 AM EDT
To Register Free: www.pharmtech.com/manual |
FDA Publishes Additional Guidance on Refuse-to-Receive Standards
FDA releases guidance on ANDAs and PASs submissions to help applicants avoid deficiencies.

Molecular Profiles Expands Capsule Capability
Molecular Profiles has expanded its capsule filling capability following significant investment into new equipment at its clinical manufacturing site in the United Kingdom.

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PharmTech Europe
25th Anniversary
Pharmaceutical Technology Europe celebrates 25 years of publishing with a retrospective of drug development trends and expert insight into emerging trends.
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Pharmaceutical Technology presents its Process Analytical Technology resource guide combo
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 |
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