The innovation debate (Why isn’t there more or it? How much should we pay for it? Just what is it anyway?!) remains a lively one in the UK. Lord Saatchi’s Medical Innovation Bill is just one part of this debate.
The innovation debate (Why isn’t there more or it? How much should we pay for it? Just what is it anyway?!) remains a lively one in the UK. Lord Saatchi’s Medical Innovation Bill is just one part of this debate. It’s intended to mitigate against so called ‘defensive’ medicine, where clinicians might not prescribe or undertake surgery that differs from the ‘standard’ because they fear prosecution.
The Bill is still progressing through the House of Lords. In part, progress has been helped by the introduction of amendments, ‘safeguards’ to guard against quackery. The latest of which was just prepared on November 20, 2014. These amendments seem to have won over some of the detractors.
The Bill is still a long way from becoming law; the next stage is a reading in the House of Lords tabled for December. Outside of Westminster the campaign rolls on using very modern PR tactics, including a petition on change.org (with 19,913 supporters so far) and with the Saatchi team encouraging people to email and tweet their MP.
Concerns abound though; detractors say there isn’t compelling evidence that defensive medicine is a barrier to innovation, for others that the current legal framework already allows doctors to prescribe outside of licenses, and even before a license is available, so the Bill isn’t actually needed. More worrying is that some say that it could cause harm from rogue doctors who experiment irresponsibly.
Given the very modern way that the Saatchi team are promoting the Bill, the docs too are trying their hand at modern PR and have now set up their own website, to point out their concerns, as well the more traditional route of writing to The Times. The Lancet has also waded in, suggesting that the Bill strikes at the heart of evidence-based medicine.
The debate has become heated (and creative, some call it the Quacks Charter, others the Medical Anecdote Bill) with the risk that it becomes less about patients, and more about the personalities involved. I can’t help but wonder about the opportunity cost of all this campaigning and parliamentary time, would it have been better to have put the time and money into research to treat rare cancers?
Leela Barham is an independent health economist. You can find out more about on her here and contact her at leels@btinternet.com
Addressing Disparities in Psoriasis Trials: Takeda's Strategies for Inclusivity in Clinical Research
April 14th 2025LaShell Robinson, Head of Global Feasibility and Trial Equity at Takeda, speaks about the company's strategies to engage patients in underrepresented populations in its phase III psoriasis trials.
Beyond the Prescription: Pharma's Role in Digital Health Conversations
April 1st 2025Join us for an insightful conversation with Jennifer Harakal, Head of Regulatory Affairs at Canopy Life Sciences, as we unpack the evolving intersection of social media and healthcare decisions. Discover how pharmaceutical companies can navigate regulatory challenges while meaningfully engaging with consumers in digital spaces. Jennifer shares expert strategies for responsible marketing, working with influencers, and creating educational content that bridges the gap between patients and healthcare providers. A must-listen for pharma marketers looking to build trust and compliance in today's social media landscape.
Pfizer, GSK Gain ACIP Recommendations for RSV and Meningococcal Vaccines
April 18th 2025The Centers for Disease Control and Prevention’s Advisory Committee on Immunization Practices voted to expand access to Pfizer’s respiratory syncytial virus vaccine Abrysvo for high-risk adults in their 50s and voted in favor of GSK’s meningococcal vaccine, Penmenvy, for streamlined adolescent protection.