News - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

News


Pharmaceutical Technology Europe
Volume 23, Issue 11

News bites

EMA invites feedback
The EMA released two concept papers for a 3month public consultation that address the need to revise existing guidelines on biosimilar medicines and influenza vaccines. Feedback can be submitted until 31 December 2011.

Read more at: http://www.pharmtech.com/EMApapers

AstraZeneca in China
AstraZeneca is investing $200 million in a new manufacturing facility in China for intravenous and solid medicines. The facility will be located in Taizhou, with construction due to finish at the end of 2013, and will help the company to expand its medicines availability in urban and rural communities.

Read more at: http://www.pharmtech.com/azinchina

GSK and fast cars
GSK has formed a long-term partnership with the UK-based McLaren Group, which is best known for its expertise in the Formula 1 motor sport. McLaren will share its capabilities in engineering, technology, analytics and strategy modelling to help improve GSK's manufacturing, R&D and consumer-healthcare areas.

Read more at: http://www.pharmtech.com/formula1

FDA enhances database
The FDA is considering whether to enhance its inspections database by adding specific search criteria that would both enhance data analysis and make the system more user friendly. The idea was included in a list of eight draft proposals for increasing transparency that the agency published in October.

Read more at: http://www.pharmtech.com/fdasearch

Sign up for our weekly e-Alert at http://www.pharmtech.com/signup


ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
How does your company apply quality-by-design (QbD) principles to manufacturing processes?
To all processes for both new and legacy products
To all process for new products only
To select process for new products only
To select processes for both new and legacy products
Do not use QbD
To all processes for both new and legacy products
18%
To all process for new products only
13%
To select process for new products only
22%
To select processes for both new and legacy products
22%
Do not use QbD
24%
View Results
UPCOMING CONFERENCES

Programs for Investigational and Pre-Launch Drugs
Philadelphia, PA
July 17-18, 2013
Request Brochure

Strategic Pipeline Planning & Portfolio Valuation
Philadelphia, PA
August 13-14, 2013
Request Brochure

MES 2013 - Forum on Manufacturing Execution Systems
Philadelphia, PA
August 14-15, 2013
Request Brochure

Mobile Innovation for the Life Sciences Industry
Philadelphia, PA
August 20-21, 2013
Request Brochure

See All Conferences >>

Eric Langer Outsourcing Outlook Eric LangerOutsourcing's Modest Role as a Cost-Containment Strategy
Patricia Van Arnum Ingredients Insider Patricia Van ArnumIntellectual Property Battles in Solid-State Chemistry
Nathan Jessop Industry Insider Nathan Jessop Campaign Against Counterfeit Drugs Continues
Lynn Torbeck Statistical Solutions Lynn D. TorbeckCompositing Samples and the Risk to Product Quality
 More
Inadequate Access to Medicines Puts EU at Risk
FDA Offers Insight on QbD for Modified-Release Products
Global Biosimilars Market to Reach $2.445 Billion in 2013
Adapting to Change
AstraZeneca and Exco InTouch Collaborate to Augment Current COPD Pathways
FindPharma Custom Search
Source: Pharmaceutical Technology Europe,
Click here