A report from the European Union Intellectual Property Office shows that the EU loses approximately €10.2 billion a year due to counterfeit medicines. / read more /
The time and resources required to finalize post-approval changes may be preventing manufacturers from modernizing facilities, or even scouting for new technology. / read more /
EDQM and the Japanese Pharmacopoeia will improve the sharing of information on therapeutic products that are common in both Europe and Japan. / read more /
Allergan entered into a licensing agreement with AstraZeneca for MEDI2070, an anti-IL-23 monoclonal antibody in phase IIB development for the treatment of patients with moderate-to-severe Crohn's disease. / read more /
PharmTech's 2016 survey shows general satisfaction with existing solid-dose and parenteral manufacturing equipment, and slow adoption of continuous manufacturing processes. / read more /
INJECTA ABITEC Corporation is dedicated to the advancement of essential bioavailability enhancement and formulation development technology. ABITEC synthesizes and produces lipid based excipients to enhance bioavailability of poorly water soluble and poorly permeable molecules for the pharmaceutical industry. / Read more/
EtQ Reliance Solution for Life Sciences
EtQ is the leading Quality, Compliance and EHS Management software provider for identifying, mitigating and preventing high-risk events through integration, automation and collaboration. / Read more /
Date: 21-23 November 2016 Venue: Bombay Exhibition Centre, Goregaon, Mumbai and MMRDA Grounds, BKC, Mumbai
The Indian pharmaceutical industry is all set to experience South Asia's largest Pharma event CPhI and P-MEC 2016, which will be concurrently held at the Bombay Exhibition Centre (BEC) and Bandra Kurla Complex (BKC) in Mumbai. / Read more /
Don't Let the Diluent be Your Weakest Link in Your Drug Product
Live Webinar: Thursday, October 13 at 10:00am EDT Asia/Pacific Session: Thursday, October 13, 2016 at 3:00pm SGT (Singapore)/ 4:00pm JST (Tokyo/Korea) US/EU Session: Thursday, October 13, 2016 at 10:00am EDT (New York City)/ 3:00pm BST (London)/ 4:00pm CEST (Berlin) Register now
A compilation of informative, useful articles designed to help you meet the challenges of process analytical technology, be more efficient in testing, reduce over-processing, enhance consistency, and minimize rejects. / Click here /
Read feature articles on accelerated scale-up for vaccine production, standards for air cleanliness classification, aseptic filling advances, a flexible approach to cleanroom design, a science-driven approach for microbial control, removing genotoxic impurities, regulatory enforcement, drug shortages, and validation of single-use shipping systems.
