SPOTLIGHT -
November 19th 2024
As skepticism surrounding AI fades, pharma industry execs are ready to embrace the technology.
November 15th 2024
Ann Beliën, PhD, founder and CEO of Rejuvenate Biomed, discusses how AI is being used to find new ways to treat age-related conditions.
November 14th 2024
Exploring those areas and functions where the application of generative artificial intelligence—through use cases borne out in practice—are demonstrating tangible value and driving life sciences innovation to new heights.
Pleio’s chief experience officer discusses why these platforms are being embraced by the industry.
November 13th 2024
Pharma looks to take advantage of expanded access programs across Asia-Pacific region.
FDA Releases Final Biosimilar Guidance
FDA releases long-awaited guidance documents regarding the assessment of biosimilarity.
FDA Fast Tracks Development of Sanofi Rare Disease Treatment
April 28, 2015.
The UK BioIndustry Association's Vision for the Sector in 2025
AZ Deal Fuels Innate Pharma Share Surge
April 27, 2015.
Pharma's $462 Billion of M&As Since Jan 2014
Medical Apps Tricky for Pharma
The industry continues to puzzle over FDA's proposed regulation of mobile medical apps (MMAs), writes Jill Wechsler.
Newer Companies Shaking Up the Pharma Industry, Reports WSJ
April 24, 2015.
Teva Acquisition of Mylan "Could Transform Generics Space"
Advancements and Acquisitions Fueled Mid-Cap Biotech R&D Spend in 2014, Says Report
April 23, 2015.
Teva's $40 Billion Bid for Mylan
Teva announces that it would pay up to $40 billion in cash and stock to acquire Mylan.
Marketing Authorization More Likely for Companies Following EMA Clinical Development Plans
The European Medicines Agency releases findings from marketing authorization application analysis.
European Body Warns of "Antibiotic Armageddon"
April 21, 2015.
FDA Releases Draft Guidance on Promotional Labeling and Advertising
The agency has released draft guidance on providing regulatory submissions in regards to promotional labeling and advertising materials.
US Marshals Seize Unapproved Drugs
At the request of FDA, US Marshals seize unapproved prescription drugs from Florida distributor.
WHO Pushes for Prompt Reporting and Public Disclosure of Clinical Trial Data
WHO says that results from clinical trials should be reported within 12 months of completion of the study
FDA Extends Comment Period on ANDA Rule
FDA extends ANDA rule comment period to June 8, 2015 after requests for more time.
Record US Drug Spend in 2014
April 16, 2015.
India May Take WTO Action after EMA Drug Suspension
Pfizer Announces PCSK9 Competitive Grants Program
The grants will be offered to investigators conducting research in the field of PCSK9 biology.
Mylan Offers $29 Billion for Perrigo
Mylan announces that it would offer Perrigo $29 billion in cash and stock to buy the Irish company.
Diverse Pipeline "Could Transform Liver Cancer Treatment" Within 10 Years
April 7, 2015.
Novartis and Juno Settle Over CAR-T Therapy Technology
Novartis will make payments to Juno to settle a patent dispute covering chimeric antigen receptor T-cell (CAR-T) therapies.
GSK Announces US Vaccine R&D Center
GlaxoSmithKline announces global vaccines research and design facility to be based in Rockville, MD, USA.
More Incentives for Antibacterial R&D
March 31, 2015.
Five Indispensable Lessons from SXSW
Janelle Starr was surprised to find this month's SXSW speakers talk about failure. But their failures are enlightening, and essential to their ultimate success.
Is the Cost of Drug Development "Accurate"?
March 20, 2015.
ASCO Report Shows Widespread Disturbance in Oncology Practice
18 March, 2015.
PPACA to Help Drive US Pharma Market to $550 Billion by 2020
March 17, 2015.
Valeant Raises Offer for Salix
16 March, 2015.
UK Life Sciences Sector Sees "Resurgence" in Financing
March 16, 2015.