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When you seek accurate, customized, and actionable recommendations tailored to your business needs, turn to the experts at Informa Pharma Consulting. Providing pharmaceuticals consulting, medtech consulting, and life sciences consulting, our Pharma Consulting London office provides global pharma consulting services and has worked with Big Pharma, mid-tier, biotech, and generics players, as well as medical device companies.  With experience in conducting business in all key geographies, Informa consulting draws on the unparalleled data and analysis offerings from across the Informa family of intelligence products, and offers pharma consulting solutions to all your Portfolio Management, R&D Strategy, and Commercial Optimization needs.

Pharma Consulting Whitepaper

Accurate benchmarking has never been more important to the biopharma industry than now, with increased scrutiny related to development costs at an all-time high. What benchmarks are you using? How does your development program compare to those of your competitors?

Explore the importance of benchmarking, specificity, and consulting as they relate to drug development approval rates in biopharma with Pharma Consulting - Probabilities of Technical Success in Biopharma, the informative whitepaper from Informa’s Pharma Consulting.


In this free resource, you’ll discover vital information to help you understand the critical importance of questions like:

  • Do you trust that your decisions are being made based on sound data?
  • Are you able to drill down into and understand the specifics behind trials and programs that succeeded as opposed to ones that failed?
  • Do your benchmarks provide the “why” behind the numbers?

Pharma Intelligence latest insights

  • Biomedtracker

    Clinical Trials Industry Report

    By KNect365 17 Aug 2018

    Clinical trials are continually evolving, particularly in light of increasing pressures from new technologies and other disruptors. Trends ranging from artificial intelligence (AI) and mHealth to patient-centricity are challenging the industry to innovate against the backdrop of looming regulatory changes and shifting competitor landscapes resulting from M&A activity. In order to explore these trends, KNect365 Life Sciences recently conducted one of the biggest surveys of its kind across clinical trial professionals from within pharma, CROs, sites, service providers, academia and patient groups across the world to look beyond the hype.

    Topic Clinical trials Clinical trial optimization

  • Pharma Consulting

    Changing the future of data

    17 Aug 2018

    With fewer successful drug launches in the market and expiring patents, competitive intelligence and commercial R&D decision makers are hard-pressed to make sound forecasting and planning decisions based on highly reliable data analysis. That’s a big challenge because, even with access to big data from many sources, the tasks associated with collecting, organizing and mapping data sets is time-consuming, costly and labour-intensive. As result, decision making takes longer and innovation suffers.

    Topic Business strategies Company analysis

  • Scrip

    Amicus' Oral Fabry Drug Priced To Compete Against Traditional ERT

    By Jessica Merrill 17 Aug 2018

    FDA approved Galafold under accelerated approval, paving the way for the launch of the first oral therapy to treat a subset of patients with the rare condition Fabry disease. Amicus priced Galafold at $315,000 per year.

    Topic FDA

  • Scrip

    Sensyne Health CEO Drayson Says IPO Will See AI Group To Profitability

    By Sten Stovall 17 Aug 2018

    Flush with IPO funding, AI-focused healthcare technology group Sensyne Health will now ready additional products and find three more NHS trust partnerships. CEO Lord Drayson spoke to Scrip.

    Topic Research Business strategies

  • Medtech Insight

    QSR Author Kim Trautman Predicts What A Mash-Up Of FDA's Quality System Regulation And ISO 13485 Might Look Like

    By Shawn M. Schmitt 17 Aug 2018

    US FDA will face high hurdles as it works to write a new rule that would merge the agency's Quality System Regulation with international quality systems standard ISO 13485. That's according to Kim Trautman, a longtime industry insider who wrote the QSR in the early to mid-1990s. "It’s a clear heavy lift from a regulatory policy perspective" that could take as long as five years to complete, she says. In the meantime, Trautman offers some insight into what device-makers might see in a new hybrid quality systems regulation from FDA. She addresses everything from corrective and preventive action (CAPA) to labeling, and complaint handling to risk management – and more.

    Topic FDA

  • Medtech Insight

    Pre-Certs, Test Groups And More: US FDA Outlines Possible New Dx Paradigm

    By Sue Darcey 17 Aug 2018

    The agency has responded to a draft diagnostics reform bill in Congress with proposed reforms that diverge some ways from the proposed legislation, but stick with the underlying goal of completely remaking how lab tests, including test kits and lab-developed tests, are regulated. The agency has put forward a proposal to establish a pre-certification process for test developers, divide most tests into high- or low-risk categories (but exempt many from pre-market review) and remove the concept of substantial equivalence.

    Topic FDA

  • Rose Sheet

    GC3 Announces Preservative Challenge Winners

    By Ryan Nelson 17 Aug 2018

    Avisco, a biotech startup focused on the antimicrobial properties of the Inula viscosa plant, and IMD Natural Solutions, whose INS Glycolipid mushroom extract purportedly is “up to 80 times more effective than traditional preservatives,” are among winners named Aug. 6 by GC3.

    Topic BioPharmaceutical

  • In Vivo

    True Innovation In Women's Health Hindered Because Conditions Are Not Fatal

    By Lucie Ellis 17 Aug 2018

    Drug developers and financiers discuss the biggest challenges delaying novel R&D in diseases effecting only women and how poor awareness of the debilitating symptoms that come with some conditions has led to a lack of emphasis on innovative research.

    Topic Drug approval Drug review

  • Biomedtracker

    Biomedtracker 2018 Early Outlook Report

    15 Aug 2018

    What's on the horizon for pharma in 2018? Find out with Biomedtracker's Early 2018 Outlook Report extract. Download free extracts from this essential report, which investigates the catalysts expected to occur in the first part of the year for 21 different drugs.

    Topic Drug development landscape

  • Biomedtracker

    Biomedtracker Q3 2018 Outlook Report Extract

    15 Aug 2018

    Download an extract of the data-rich resource: Biomedtracker’s Q3 2018 Outlook Report. This latest installment in Biomedtracker’s ongoing quarterly reports contains expected drug catalyst predictions, important clinical and regulatory milestones, and Large Impact catalysts for the upcoming quarter. 

    Topic Drug development landscape

  • Meddevicetracker

    Meddevicetracker Q3 2018 Outlook Report Extract

    14 Aug 2018

    In this report, we cover catalysts from 10 devices expected to occur in Q3 2018. These include important regulatory milestones and trial data across the cardiovascular, neurology,  and endocrine (including diabetes) spaces. Additionally, at the end of this report we have included a list of Large Impact catalysts through Q3 2018.

  • Scrip

    Perrigo Looks To Spin Out Or Sell Off Rx Business, But Will Separating Generics Add Value?

    By Mandy Jackson 14 Aug 2018

    Perrigo previously saw value in keeping its prescription pharmaceuticals in-house, but now says it will sell off or spin out the topical generics to focus on its over-the-counter brands. Questions remain about whether the company's generics portfolio is valuable enough to stand alone or attract a buyer.

    Topic Business strategies Drug approval

  • Scrip

    A Safe Harbor For Biotechs Ascletis BeiGene Mark Early Wins For HK Exchange

    By Jules Quartly 14 Aug 2018

    The market debuts of BeiGene and Ascletis on the new Hong Kong Stock Exchange’s Biotech section could further encourage other Chinese biotech companies as they seek to draw in a wider pool of investors and focus on the promising domestic sector.

    Topic Business strategies Company analysis

  • Pink Sheet

    US FDA’s Breakthrough And RMAT Designations: A Quick Guide

    By Bridget Silverman 14 Aug 2018

    Differences in eligibility and evidentiary criteria between the US FDA's two expedited regulatory programs are reflected in a new guide; metrics to date suggest comparable success rates for designation requests under the two programs. Our infographics aid in understanding the programs.

    Topic FDA

  • In Vivo

    Cancer's New Patient Demographic; Will Survivorship Change The Face Of Cancer Care?

    By William Looney 13 Aug 2018

    The 16 million survivors of cancer in the US today form a restless constituency with its own disparate set of interests – and by sheer weight of numbers is beginning to direct changes to medical practice that pose both risks and opportunity for biopharma.

    Topic Cancer

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