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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 to be more efficient in testing while at the same time reducing over-processing, enhancing consistency and minimizing rejects.
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FDA Urges Greater Focus on Contractor Quality
Increased manufacturer outsourcing requires clear policies and written agreements with CMOs.
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Life Sciences Guidebook: Best Practices for FDA Compliance Solutions
This guidebook provides you with a basic overview for selecting, implementing and using FDA Compliance and Quality Management solutions. Learn the importance of QMS, best practices for FDA Compliance and Quality systems, and tips and tricks for finding the solution best suited for your company. Read More |
EU Battles Medicine Shortages
European governments are under pressure to take regulatory action, but solving the problem of medicine shortages is not as straightforward as it seems.

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Get Your Equipment CLEANER, FASTER!
Clean, rinse and dry your manufacturing equipment in minutes! Your cleaning process doesn’t have to be a hassle — get a more thorough cleaning in 3 easy steps. Learn More! |
Regulatory Roundup
Compounding, tracking legislation moves forward

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Nippon Soda Co., Ltd.
Nisso HPC-SSL-SFP (special low viscosity, super fine powder grade) is introduced as a dry binder for direct compression, ODT and extra-granule addition applications. The excellent tablet properties that HPC is known for as a wet binder can now be achieved in dry binding applications using very low levels (3%-7%) of binder, while disintegration times and drug release are super fast. www.nissoexcipients.com |
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1-Hour Webinar: Validation/Mapping Protocols
Get this on-demand Webinar on best practices for creating protocols for environmental validation applications. Here’s what webinar attendees said:
“Webinar was awesome...Thanks for sharing best practices in industry and regulatory expectations and good compliance practices.”
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Watch this Recorded Webinar… |
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What is the single greatest threat to maintaining manufacturing processes at your facility?
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Overcoming Challenges in Development of Oral Enteric and Controlled-Release Dosage Forms
Live Webcast: Thursday, July 18, 2013 at 11:00 am EDT. Register Free at:
www.pharmtech.com/overcoming |
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