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  Pharmaceutical Technology Europe E-Alert
 
14 September 2012
IN THIS ISSUE
Pharmaceutical ingredients
Paediatric medicines
Highly potent APIs
Cargo theft
News
 
Insight into Pharmaceutical Ingredients
With CPhI just around the corner, we've made pharmaceutical ingredients the focus of the September issue of PTE Digital. In particular, experts examine the challenges of highly potent ingredients. In addition, this month's issue covers paediatric medicines, the problems of tablet sticking and cargo security. More...
 
Regulatory Intervention in Paediatric Medicines
Regulators have attempted to stimulate paediatric-drug development with incentives offering extended periods of patent protection, but are these actions having the desired effects? Nathan Jessop examines the concerns of some in the industry who believe these incentives may be being misused. More...
 
Strategies for High Containment
In this roundtable, experts share insight on facility design and operations for high-potency manufacturing, including the main considerations in equipment and facility selection, as well as how to effectively monitor and control risk. More...
 
Pharmaceutical-Based Cargo Security and Theft Prevention
A rise in the incidence of cargo thefts in the pharmaceutical industry requires a cross-functional response from individual companies, the industry, law-enforcement organisations and other stakeholders. The author discusses strategies for a proactive cargo security and antitheft program, including best practices used by Pfizer. More...
 
News Bites and Twitter Trends
If you’ve missed out on some of the top news stories about the pharmaceutical industry recently then our news roundup will update you. Highlights include GSK divestures and the UK’s high-tech stem cell centre. We also bring you a summary of some of the latest headlines from Twitter. More...

Key Topics:
Latest blog posts
LIVE from PDA FDA Joint Regulatory Conference 2012
Be Prepared
Omega-3s Prescription Products: A Case Study of Innovation
More blog posts

Latest news
Pfizer Settles Patent Litigation with Mylan
CDER to Expand Office of Generic Drugs
Eli Lilly Receives FDA Warning Letter
More news

Upcoming events
Biosimilars and Biobetters (24–25 September | UK)
BioPartnering FurtureEurope (7–9 October | Belgium)
CPhI Worldwide (9–11 October | Spain)
More events

Products/Service Profiles
Agilent

Realize Effective Pharmaceuticals
Reliable solutions enable pharmaceutical scientists to innovate in disease research, accelerate drug discovery and have greater confidence throughout development and manufacturing. Agilent solutions in genomics research, automation, separation and detection technologies along with workflow driven software solutions helps deliver the answers to bring effective therapeutics to market.
Learn more at www.agilent.com/lifesciences/realizepharma

 
Agilent

Agilent ICP-MS/ICP-OES
Reliable solutions for regulated pharmaceutical laboratories

Complying with new elemental impurity limits as defined by draft USP methods <232>/<233> could pose a significant challenge. You need to choose qualified hardware and software, ensure verification, and maintain electronic records. But there is a simple answer – Request a free copy of our primer on Elemental Impurity Analysis to learn more.

 
BASF SE, G-ENP/K

Ludiflash® is a combined filler, binder and disintegrant that is used to create fast-dissolving, fast-acting formulations with an exceptionally smooth and creamy mouthfeel. Read more


Event Profile
Perkin Elmer

3 Live Webinars coming soon.
Supply chain security - how best to use the most important tool in supply chain protection
Infrared spectroscopy is the most economical way to screen against many of the risks that exist today in your supply chain of raw materials – counterfeit, contaminated, adulterated, diluted, substituted, false claims of purity/source etc.
Read more

 
CPHI Worldwide

CPhI Worldwide is the world’s leading pharmaceutical networking event for Pharma Ingredients.  Along with co-located events ICSE for Contract Services, InnoPack for Innovative Packaging and P-MEC Europe for Technology, Equipment and Machinery, this is a one-stop shop event that cannot be missed by anyone serving the (Bio)Pharmaceutical industry.
Read more

 
 
Survey
Has your company started implementing procedures and practices required by Europe's new pharmacovigilance legislation?
 
Yes 85%
 
 
No 5%
     
 
We are making progress 10%

This week we would like to know...

What do you think will be the greatest benefit of FDA's Generic Drug User Fees Amendments of 2012 (GDUFA)?

Click here to vote

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