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  Pharmaceutical Technology Europe E-Alert
 
8 April 2014
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Featured Topics
A New Approach to Forced Degradation Studies Using Anhydrous Conditions
In this article, the authors demonstrate that a normal-phase chromatographic method was stability-indicating for a water-sensitive prodrug. The stress conditions using aqueous and non-aqueous conditions were also compared to understand the information obtained with each approach. More...
 
Best Practices in Adopting Single-Use Systems
Bioprocessors should understand the key factors associated with implementing single-use components or platforms, which include materials of construction, components, system design, and vendor support. More...
 
Separation of Compliance and Performance Under FDASIA
The root cause of drug shortages is mismanagement of variation. More...
 
FDA Wants You!
A number of top management positions at the Center for Drug Evaluation and Research (CDER) need to be filled, and CDER leaders are looking for experienced industry managers to help rebuild its staff. More...
 
Top Stories
Sun Pharma to Acquire Ranbaxy
Sun Pharma acquisition of Ranbaxy Laboratories will create the fifth-largest specialty generics company in the world. More...
 
Merck Announces Management Changes
Merck promotes internal managers to head Merck Millipore and Consumer Health Divisions. More...
 
EDQM Launches Counterfeit Drug Database
EDQM has launched a database, Know-X, which collates reports on counterfeit/falsified medical products that have been detected in Council of Europe member states. More...
 
FDA Allows Imported Saline to Address Shortage
FDA has announced Fresenius Kabi USA, LLC of Lake Zurich, Ill., will temporarily distribute normal saline in the United States from its Norway manufacturing facility. More...
 
A New Plant Biotech Approach for Efficient Production of Pharmaceutical Compound
European scientists have discovered a method to improve the efficiency of the pharmaceutical production through plant biotechnology. More...
 
FDA Approves Auto-Injector to Reverse Opioid Overdose
Evzio, the first naloxone treatment specifically designed to administered to opioid overdose patients by family members or caregivers, approved in 15 weeks. More...
 
Industry News
ChemCon Passes its Fourth FDA Inspection
ChemCon passes its fourth FDA inspection in the 17-year history of the company. More...
 
AmerisourceBergen Acquires Minority Interest in Profarma
AmerisourceBergen to establish a joint venture for specialty distribution with Profarma. More...
 
Carolina Medical Products Renamed CMP Pharma
 Carolina Medical Products changes its name to CMP Pharma to reflect current business trends. More...
 
Dalton Pharma Completes Aseptic Filling Capabilities Expansion
Dalton Pharma completes its $2.5 million expansion in Toronto for sterile and aseptic filling capabilities. More...
 
Webcasts
New Strategies for Evaluating BioPharmaceutical Stability
On Demand
Sponsored by: ABC Labs
 
A Pragmatic Application of QbD: Turning Theory into Tangible Success
On Demand
Sponsored by: Patheon
 
USP Outlook: Key Program Activity for 2013
On Demand
Sponsored by: USP
 
More Webcasts

Product Profiles
Agilent
Agilent Solutions for Quality by Design
Agilent’s new QbD Solutions Guide provides information about Agilent tools and technologies to help you minimize variability in analytical method development and analytical method transfer, and support quality by design implementation.   Agilent strives
to provide solutions you need to be successful, and to earn
your trust as a partner in implementing solutions. Download your guide here.
ETQ
Life Sciences eBook: Best Practices for FDA Compliance
In a market where high-demand causes organizations to seek software systems that will fit into their complex business infrastructure, the pressure to find the right system often causes angst to many.
Learn some key elements to spotting a good FDA Compliance solution, techniques for achieving Good Manufacturing Practice Compliance, and how to ensure that Quality and Compliance are met in the Life Science
industry. Read more
Shimadzu
Trace level quantitation of multiple compounds
Shimadzu’s LCMS-8050 triple quadrupole LC-MS/MS meets the growing demand for trace-level quantitation in clinical research and other markets. It incorporates proprietary ultrafast technologies as well as a newly developed ion source and collision cell technology. Read more
DIOSNA Dierks & Söhne GmbH
Mixing, Granulating, Drying & Coating
DIOSNA presents a compact, closed granulation line in "Rapid Change" design. It is a complete system for mixing, granulating and drying of pharmaceutical products in the field of R&D and clinical samples. Read more
Eurofins Scientific
Bio/Pharmaceutical GMP Product Testing
Eurofins BioPharma Product Testing is the largest network
of harmonized bio/pharmaceutical GMP product testing laboratories worldwide providing comprehensive
laboratory services for the world’s largest pharmaceutical,
biopharmaceutical and medical device companies. Read more
 
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Reference Library

Pharmaceutical Technology Solid Dosage Combo
Increase your knowledge of solid dosage technology and solid dose tablet manufacturing processes. These comprehensive pharmacology reference guides cover a variety of solid-dosage form principles such as oral solid-dosage forms, powders, mixing and blending, excipients, tableting, and coating. Drug delivery system manufacturing professionals can use the solid dosage manufacturing books to stay current with compressed tablet manufacturing processes, solid dosage processing equipment, tablet-pressing processes, and pharmaceutical industry trends in oral solid dosage manufacturing and solid dosage form development. ... Click here


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