Imperial Recognized as 2025 Best & Brightest Company to Work For in West Michigan! Learn More

Imperial Clinical Research Services Blog
  • Services
    • What We Do
    • Study and Site Print Materials
    • Clinical Trial Translation Management
    • Ancillary Trial Supplies and Equipment
    • Clinical Trial Patient Engagement
    • CRO-Centered Services
    • A La Carte Services
  • Resources
    • Ebooks
    • Case Studies & Fact Sheets
  • About
    • About Us
    • News
    • Events
    • Corporate Responsibility
  • Contact
    • Contact Imperial
    • Career Opportunities
  • Blog
  • Marketplace
  • Services
    • What We Do
    • Study and Site Print Materials
    • Clinical Trial Translation Management
    • Ancillary Trial Supplies and Equipment
    • Clinical Trial Patient Engagement
    • CRO-Centered Services
    • A La Carte Services
  • Resources
    • Ebooks
    • Case Studies & Fact Sheets
  • About
    • About Us
    • News
    • Events
    • Corporate Responsibility
  • Contact
    • Contact Imperial
    • Career Opportunities
  • Blog
  • Marketplace
Author

Imogen Cheese

Imogen Cheese

Imogen is Imperial’s director of business development for the U.K. and Europe. She has 20 years of business management experience with a deep understanding of trial setup and recruitment in the clinical sector. She is the founder and director of Melanoma Patient Conference CIC, a non-profit education and support group that holds an annual conference for 300 melanoma patients. Imogen is an energetic advocate for the patient community, frequently speaking internationally at events, and providing guidance for ongoing initiatives impacting patients. She believes an informed patient is the best partner for long-term success in clinical trials.

    Business Insights

    Brexit, Medicines, and Trials: A Report from the U.K.

    by Imogen Cheese March 12, 2019
    written by Imogen Cheese

    Several members of my family live in mainland Europe and join huge numbers of British expats concerned about how Brexit will impact their daily lives. My father, who takes a daily medication to treat his prostate cancer, fears the potential impact on reimbursement and therefore his long- term survival.

    Here in the U.K., there have been rumblings for some time about stockpiling medications and the possibility of a shortage of supply as the borders and import/export regulations change. The U.K. government launched plans to fly in emergency supplies and have drawn up risk scenarios for drug rationing. The slow drip-feeding of this information through the media has caused great concern and anxiety for the patient community.

    With the final decision about what type of Brexit we will have, which is still very much under debate, and with the deadline looming closer, the supply of drugs has already become a problem. There are now over 85 common drugs in short supply across the U.K., and the price of hundreds of other key drugs have increased exponentially to meet with the demand.

    Some pharmacists have reportedly contacted the National Health Service (NHS) in England with grave concerns about the impact of missed treatments for many of their patients. There are cynics who claim the increased costs are merely opportunism and pessimists who declare that the current state of the drug supply is the tip of the iceberg. They say that within months it won’t be common drugs that the U.K. will face supply issues with, it will be cancer treatments and even the supply of drugs for clinical trials.

    Over the last year, I have had several conversations with colleagues discussing how best to manage the impact of Brexit upon clinical trials. I know of several studies that have been delayed while awaiting the decision. Other clients have expressed fears of increased costs with the supply of trial materials in and out of the U.K. and how this affects the placement of study sites.

    The final closure last month of the European Medicines Agency offices in the U.K. was a monumental event as the industry witnessed the departure of colleagues and friends moving to Amsterdam. The 1,000 people who worked at the EMA offices faced relocation or job changes, which impacted their lives and those of their immediate families. Local businesses face the loss of income generated by the 36,000 regulators and scientists that would visit the EMA annually, a painful long-term impact on the U.K. economy. To many, this felt like a backward step in progress and collaboration.

    Cancer Research UK published an advisory report last year to the U.K. government that covered all aspects of the potential risk of a hard Brexit, from staff shortages and drug supply to research collaboration. In 2017, there were 823 applications for commercial trials of medicines in the U.K. Eighty percent of clinical trials are global, so it is in the long-term interest of medical research and the patient community for the effect of Brexit to be both short lived and where possible, negated.

    I sit in a unique position of working within the industry and therefore understanding the commercial risks and impacts of Brexit and also the more personal and emotional position as a patient and advocate.

    Patients fear stagnation in clinical research. With international cooperation comes progress and great strides forward in the development and bringing to market of new innovative treatments. Will the disjointing effect between the U.K. and the EU have a detrimental impact on clinical research?  Will the impact of Brexit cause so much undue bureaucratic red tape that patients in the U.K. will have to wait longer than our counterparts on the continent to obtain access to trials, treatments, and new drugs?

    The most likely scenario is that there will be a significant impact no matter the outcome of Brexit. There will be delays, new systems, processes and laws which need to be created, absorbed into policy, and adjusted to. This will not be an overnight process and there simply is no way to fully prepare for these eventualities. We can already feel the shift in recruitment and the already overstretched NHS bracing itself for the harsh negative impact.

    In a recent article, David Meek, CEO of Ipsen, warned that leaving the EU will affect the buying power and position of the U.K. government to obtain the same prices and supply levels of key approved drugs as we may have historically accepted. While the frustration resulting from chaos importing and exporting supplies might be short-lived, the potential longer-term ramifications that will directly impact patients continue to unfold.

    At Imperial, with our existing clients, we work to put contingencies in place. This includes ensuring sites are adequately stocked, where possible, to ensure no delays or impact to studies. We work with Brexit risk assessors in each client’s organisation to set up processes unique to them that help us manage their supply and stock effectively. Our flexibility and the immediate responsiveness of the Imperial marketplace is part of our process designed to help mitigate concerns over such delays.

    The ongoing attempts to mitigate risk and prepare for all potential eventualities is challenging, and the patient community are grateful for all attempts to minimize the storm that’s heading our way.

    Brexit has created further anxiety for patients that may already feel hopeless and lost in the system. While treatments and care pathways may be like the light at the end of the tunnel for so many, the tunnel seems longer now. We might end up as the greatest victim in this turf war, yet the irony is that as patients we exist in a constant bubble of uncertainty as our survival plays out in front of us on a daily basis, so we might actually be better able to navigate this drama than most. Patient vulnerability is both our weakness and strength, and we already anticipated a fight… because every day we live one.

    In the last week, the drama continues to unfold, with questions raised over a possible second referendum. Whatever the outcome, patients will be affected, and I will follow up after Brexit.

     

    March 12, 2019 0 comment
    0 FacebookTwitterLinkedinEmail
  • Life-Science Events

    A Cancer Patient’s Voice

    by Imogen Cheese July 10, 2018
    by Imogen Cheese July 10, 2018

    Until now I have kept my personal and professional life distinct. Since joining Imperial Clinical Research Services, the lines have blurred slightly, for the better. This has been a gradual shift, but one I was now ready to make. Recently, I was asked to speak…

    0 FacebookTwitterLinkedinEmail
  • Life-Science Events

    The Avoca Consortium Summit: My Report from Dublin

    by Imogen Cheese July 10, 2017
    by Imogen Cheese July 10, 2017

    In June, I attended the Avoca Consortium summit in Dublin on behalf of Imperial. Representatives from more than 40 companies working in pharma and biotech attended, which was quite an achievement, especially considering that many of the delegates were juggling projects between major industry gatherings…

    0 FacebookTwitterLinkedinEmail
  • Business InsightsLife-Science Events

    ESMO 2016: My Perspective as a Patient Advocate

    by Imogen Cheese October 13, 2016
    by Imogen Cheese October 13, 2016

    The ESMO, European Society for Medical Oncologists, annual conference took place in Copenhagen over an extended weekend. I was fortunate to attend as a patient advocate which was quite an honor. There were over 20,000 delegates in attendance and just 150 European patients. Imperial CRS…

    0 FacebookTwitterLinkedinEmail
  • 1
  • 2
  • 3

Welcome

Welcome

The Imperial blog features content of interest to life-science professionals, with a special focus on clinical trials. We hope you will enjoy our experts’ perspectives, and invite you to join the conversation by leaving your comments. Please let us know of any additional topics you would like to see covered here.

Signup for our Blog Subscription

Signup for our Blog Subscription

Keep in touch

Twitter Linkedin Youtube Email RSS

Popular Posts

  • 1

    See Do Get

    August 12, 2014
  • 2

    Clinical Research Phases and the Path to Drug Approval

    August 8, 2023
  • 3

    Google Translate: The Unwitting Confidentiality Flaw

    April 15, 2020
  • 4

    25 Reasons People Aren’t Enrolling in Your Clinical Trial

    October 29, 2015
  • 5

    Clinical Trial Supply Chains: The Key to Avoiding Disruptions

    May 10, 2022

Categories

  • Ancillary Trial Supplies and Equipment (28)
  • Business Insights (125)
  • Clinical Trial Writing and Design (36)
  • Life-Science Events (52)
  • Patient Engagement (31)
  • Patient Recruitment and Retention (93)
  • Site Materials & Logistics (45)
  • Study Site Management (21)
  • Translation of Study Materials (17)
Imperial Clinical Research Services Blog

Imperial is a global leader in clinical trial solutions and support, specializing in study and site print materials, ancillary trial supplies and equipment, clinical trial translation management, and clinical trial patient engagement.

Imperial CRS Corporate Headquarters
3100 Walkent Drive NW
Grand Rapids, MI 49544

Contact

connect@imperialcrs.com

800.777.2591

020 3887 3437

Employment

Social

We Run on EOS - Entrepreneurial Operating SystemEcovadis Sustainability Rating January 2024West Michigan's Best and Brightest Companies to Work For Winner 2025The Best and Brightest Companies to Work For Logo
© Imperial CRS, LLC | Privacy Policy
Signup for our Blog Subscription

Subscribe to our blog and get the latest updates, insights, and industry trends delivered straight to your inbox. Stay informed and never miss a post.