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You are here: Home > Opinion & analysis

Opinion & analysis


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  • EMA To Re-Prioritize Tasks To Cope With ‘Higher Than Expected’ Staff Losses

    $131.00

    Although original estimates put staff losses at the European Medicines Agency at about 19% due to the EMA’s relocation from London to Amsterdam, the EMA reports that these losses may actually be much higher, forcing the agency to take a hard look at its most pressing priorities moving forward.

    June 8, 2018
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  • Next-Generation Roche: How Data Analytics Will Keep It In The Lead In Oncology

    $200.00

    At Roche’s on-site investors briefing at ASCO in 2018, company execs unveiled the oncology leader’s strategy for staying ahead in the market: heavy investment in digital and personalized healthcare. Read more about the company’s plans in this illuminating article from Scrip.

    June 8, 2018
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  • Cosmetic Preservatives Crisis Creeping Into CIR Program

    $131.00

    The assessment of cosmetic preservative safety continues to be complex and fraught with controversy, as some in the industry look to the Cosmetic Ingredient Review (CIR) program to set the record straight about the use of certain cosmetic preservative ingredients.

    June 10, 2018
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  • Paying For Gene Therapy: Will Pharma Be First In Line?

    $200.00

    In considering pricing models for the increasingly important area of gene therapy, what are the options facing biopharma? This article from In Vivo explores the question of how to pay for gene therapy in a way that’s sustainable to developers of these potentially curative therapies, while ensuring patient access.

    June 12, 2018
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  • New Reasons Not To Use EU MDR’s Four-Year Extension, But Comply Earlier Or Retire Products Instead

    $200.00

    The new EU Medical Device Regulation (MDR) includes an option to market CE-marked devices for an extra four years. That extension may sound tempting, but experts advise against it. Learn about their concerns and gain insights into howto prepare for compliance under MDR.

    June 13, 2018
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  • Roche’s External Control Arms Show What Real-World Evidence Can Look Like In Practice

    $131.00

    Roche is leading the charge in the emerging field of using real-world evidence (RWE) with its recent acquisition of Flatiron Health, Inc. and Flatiron’s electronic health records database. Take a closer look at the use of RWE in actual practice in this illuminating article from Pink Sheet.

    June 14, 2018
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  • Bayer’s US Playbook: The Smart Way To Top-Line Growth

    $200.00

    Tap into Bayer AG’s plans to establish itself as a global innovator, particularly with their oncology, cardiovascular, and women’s health franchises. In this exclusive interview, In Vivo talks strategy with Dr. Carsten Brunn, Bayer’s Head of Pharmaceuticals, Americas Region.

    June 18, 2018
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  • Pharma’s New R&D Models: Federating Innovation

    $200.00

    As ROI across R&D investments in big phama declines, companies look for new and innovative ways to access and nurture innovation via partnerships and through the use of new data types.  In the process, the business models, products, and role of big pharma in healthcare is changing.

    June 20, 2018
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  • The Blockbusters No One Talks About

    $131.00

    Although their patent protection has expired, big-name blockbusters continue to produce huge revenues for the pharmaceutical companies that produce them. Take a look at how some well-known drugs may no longer be making headlines, but continue to be big earners.

    June 21, 2018
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  • It’s Complicated: FDA Prohibits CBD In Supplements, Enforcement Priority On Disease Claims

    $200.00

    The FDA recently approved its first-ever approval of a drug that contains a marijuana derivative, but the agency says that it will only focus its enforcement policy of similar dietary ingredients on products marketed with drug or disease claims. Find out more about this complex issue here.

    June 25, 2018
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  • Thinking about using CMMI? Here are tips from the experts

    $200.00

    Learn about the voluntary U.S. FDA pilot program that uses Capability Maturity Model Integration (CMMI) from quality,compliance and regulatory officials at three major device firms. Walk through the CMMI process,and discover why it’s nothing like a typical regulatory audit.

    June 25, 2018
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  • J&J Scores Early In ‘Hypoallergenic’ Case; Plaintiff’s Definition ‘Implausible,’ Court Says

    $200.00

    What’s the meaning of “hypoallergenic”? Judges in the federal court Northern District have disagreed, with a judge recently siding with Johnson & Johnson’s definition of the term as part of an ongoing lawsuit.  Find out more about the suit and its implications for your business in this article from Rose Sheet.

    June 27, 2018
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  • NASH: Flying The Plane While Building It

    $200.00

    Investors are showing interest in the development of treatments for NASH (nonalcoholic steatohepatitis), a type of liver disease, as the pipeline for the disease develops in parallel with those R&D efforts. Get a full view of the promising market for NASH in this article from In Vivo.

    July 25, 2018
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  • Cancer’s New Patient Demographic; Will Survivorship Change The Face Of Cancer Care?

    $200.00

    As the number of cancer survivors increases, they are reshaping cancer research and clinical practice. Find out how–and discover the impact it will have on the allocation of research dollars. Learn how the looming physician shortage has implications for the emergence and increasing use of complex immunotherapy drugs.

    August 6, 2018
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  • Moving Medical Affairs To The Pharma Forefront

    $200.00

    Senior medical affairs officials sat down at a roundtable discussion facilitated by the Boston Consulting Group to discuss the role of medical affairs along the pharma value chain. Take a look at the outcome of this discussion and explore the role and challenges of medical affairs in pharma.

    August 29, 2018
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