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  Pharmaceutical Technology Europe E-Alert
 
11 November 2014
IN THIS ISSUE
News
Webcasts
Events
About Us
 
 
Featured Content
The Role of Normal Data Distribution in Pharmaceutical Development and Manufacturing
Review challenges in the use of normality testing situations and recommendations on how to assess data distributions in the pharmaceutical development manufacturing environment. More...
 
Marrying Big Data with Personalized Medicine
Data analytic strategies can help companies capitalize on personalized medicine. More...
 
CMO Industry Thins Out
The trend of exits from the CMO industry looks to be gaining momentum. More...
 
Top Stories
France Agency Seeks Data from Roche on Use of Avastin in Macular Degeneration
ANSM wants company data on the benefits and risks of using Avastin over Lucentis in the treatment of wet age-related macular degeneration. More...
 
Perrigo Agrees to Acquire Omega Pharma for $4.5 Billion
The deal between the two companies will strengthen Perrigo’s presence in Europe. More...
 
PharmTech Europe Marks 25 Years of Drug Development
Biosimilar Development: 10 Years On
With a number of branded biologics hanging at the patent cliff, the future looks promising for biosimilars. More...
 
Emerging Opportunities with Biosimilars
To realise the full potential for biosimilars, stakeholders must build a better understanding of biosimilars and to take a comprehensive view of how these important medicines can fit into treatment pathways. More...
 
Blog
Combination Products Challenge Biopharma Manufacturers
Most new injectable drugs and biologics are being designed as combination therapies, presenting difficult regulatory and production issues for manufacturers. More...
 
Industry News
M&A Activity in Pharma Still Strong Despite New Tax Rules
M&A transactions accounted for nearly $15 billion more this year than for the same period a year ago. More...
 
Roche Announces 450 Million Swiss Franc Investment on New Facility
Roche announced it will spend 450 million Swiss Francs on a new manufacturing facility in Suzhou, China. More...
 
Novo Nordisk Builds New Labs in Denmark, Adds to US Staff
Construction has started on Novo Nordisk's laboratories for diabetes research in Denmark. More...
 
Hikma Pharmaceuticals Warned About CGMP Violations at Portuguese Facility
An FDA warning letter to Hikma Pharmaceuticals cites violations of CGMP at its plant in Portugal that manufactures finished drugs. More...
 
Seven Steps to Solving Tabletting and Tooling Problems—Step 2: Assess
The importance of “assessing” and how this step will help avoid any problems that may occur during tablet manufacture is discussed. More...
 
MedImmune Acquires Definiens
MedImmune enters into an agreement to acquire the image analysis and data mining company. More...
 
FDA Grants Orphan Drug Designation to Pancreatic Cancer Treatment
FDA gives orphan drug designation to Merrimack Pharmaceuticals’ MM-141 for the treatment of pancreatic cancer. More...
 
AstraZeneca Enters Collaboration with Pharmacyclics and Janssen to Test Hematologic Cancer Treatment
AstraZeneca announced a partnership with Pharmacyclics and Janssen for combination trials of MEDI4736 (AstraZeneca) with Imbruvica (Pharmacyclics and Janssen) for the treatment of hematologic cancers. More...
 
Webcasts
Developing a Comprehensive Tool Kit for Microbial Identification
Tuesday, November 18, 2014 at 8 AM CET PST/ 11 AM EST/ 4 PM GMT/ 5 PM CET
Sponsored by Eurofins Lancaster Laboratories
 
Avoiding Out-of-Specification (OOS) and Aberrant Results: Weighing and Sample Prep
On Demand
Sponsored by SGS Mettler Toledo
 
More Webcasts

Product/Service Profile
Alkermes
Dry blend tablet coating and encapsulation expertise
Alkermes Contract Pharma Services’ experience in dry blend tableting and encapsulation can provide you with expert solutions to fulfil your specific manufacturing needs.  With over 45 years’ experience, we are a proven, reliable, high quality, commercial manufacturer of choice for 7 of 10 top pharma companies worldwide. Read more
EtQ
GMP Compliance Software for Life Sciences
Professionals in Life Sciences are facing a multitude of challenges when looking to automate their systems.  Some of these include the need to eliminate manual processes and paper-based systems, being able to dig deeper into the data and make more informed decisions to help foster continuous improvement, all the while balancing cost and time savings in their efforts. Watch how EtQ’s GMP Compliance management solution provides a holistic and scalable solution for automating processes, integrating business systems and fostering continuous improvement. Read more & Watch How to Achieve GMP Compliance
 
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.
View Special Coverage

Reference Library

Pharmaceutical Technology Outsourcing Guide
Pharmaceutical Technology Outsourcing Guide provides details behind recent partnerships, strategies for selecting an appropriate CDMO/CMO, and quality by design factors for outsourced operations ... Click here

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