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Curzon Sponsors the 2024 AMBS Case Interview Competition

Curzon Consulting

17th October 2024 2 Minutes Curzon Consulting is thrilled to sponsor this year’s Alliance Manchester Business School Consultancy Case Competition. Introduced in 2016, the competition enables AMBS MBA students to showcase their skills, innovative thinking, and problem-solving abilities.

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Pharma is big business whose goal is to maximize shareholder value

World of DTC Marketing

From 2016 to 2020, the 14 leading drug companies spent $577 billion on stock buybacks and dividends—$56 billion more than they spent on R&D over the same period.” ” From 2016 to 2020, compensation for the 14 companies’ top executives totaled $3.2 Big pharma is big business.

Pharma 292
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Comparison of Humira biosimilars in the US and Europe

Pharmaceutical Technology

Biosimilars are an important tool to facilitate competition, lower the price of drugs, and create savings across the board. However, it has taken over six years for Amjevita to launch, after first being FDA-approved in 2016. Many other biosimilars have also been FDA-approved since 2016.

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Biogen’s Alzheimer’s drug: What’s the price tag on hope?

World of DTC Marketing

Since that time, Biogen’s MS drugs have faced intense competition as MS patients continue to vent on social media that the Biogen drug has nasty side effects. When you have one study that is positive and one that is negative, it seems to lead to an inability to draw a conclusion and therefore to a need for a third trial,” said David S.

FDA 187
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Rescheduling Cannabis to a Schedule III Controlled Substance: A Regulator’s Perspective

PM360

If the requirement that everything sold in-state must be grown in-state is eliminated, high cost, primarily indoor cultivation states in the Midwest and Northeast could see their entire grow industry put at an insurmountable competitive disadvantage. What’s Next if Rescheduling is Approved?

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Understanding the evidence used in drug product withdrawals

European Pharmaceutical Review

Our research showed that in Europe between 1999 and 2016, 35 products were withdrawn. Samantha leads study design and statistical analysis and has experience with the CPRD electronic health records database. 1,2 This signals a promising trend towards a more comprehensive and diversified approach in regulatory decision-making.

Medicine 116
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New Bill could enhance UK clinical trial regulation

European Pharmaceutical Review

If achieved, this would boost the UK’s competitiveness as a leading international site for trials. This is according to a 2016 paper published in Clinical and Translational Oncology. Timeframes to set up trials were reduced (on average) by 15 percent within a year of the legislation coming into force.”

Ethics 105