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Integrated Solutions for Maintaining Product Quality without Sacrificing Titer
Wednesday, July 17, 2013 at 11:00 AM EDT
Sponsored by Life Technologies

Overcoming Challenges in Development of Oral Enteric and Controlled-Release Dosage Forms
Thursday, July 18, 2013 at 11:00 AM EDT
Sponsored by Patheon

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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. ...Click here

July 11, 2013 PharmTech.com PRINT SUBSCRIBE DIGITAL SUBSCRIBE


News

FDA Urges Greater Focus on Contractor Quality
Increased manufacturer outsourcing requires clear policies and written agreements with CMOs.
Click Here to Read More

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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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Advertisement:
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:

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News

Intertek Acquires Melbourn
The acquisition of Melbourn extends Intertek's offering to include formulation, product development and characterisation of orally inhaled and intranasal products amongst others.
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Novartis and Biological E Collaborate on Delivering Affordable Vaccines
Novartis and Biological E have entered into an agreement that aims to deliver affordable and accessible vaccines for typhoid and paratyphoid A fevers to developing countries.
Click Here to Read More

Parenteral Drug Association Releases New Report on Manual Aseptic Processes
Report outlines recommended practices for control and evaluation of operations.
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Immunocore Collaborates with GlaxoSmithKline on T-Cell Receptor Technology
Research will focus on cancer and viral disease targets not addressable using antibody-based technologies.
Click Here to Read More

Literature Database for Discrete Element Method Simulation Available Online
Resource will foster innovation in DEM simulation for process industries.
Click Here to Read More

Azaya Launches New CDMO
Parexo Labs, a division of Azaya, launches as a new CDMO with an emphasis on nanotechnology and liposomal manufacturing.
Click Here to Read More

Base4 and Hitachi High-Tech Collaborate on Developing Novel Nanopore DNA-Sequencing System
The core DNA-sequencing technology is based on the concept of passing a single strand of DNA through a nanometer-scale pore and reading out the sequence directly as it does so.
Click Here to Read More

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Advertisement:
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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