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Hale House opens as new health tech innovation hub in Harley Street Health District

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Hale House is set to position the Harley Street Health District as a leading cluster for Health innovation.

The £52 million investment is a clear reflection of Howard de Walden’s ongoing commitment to advancing healthcare and solidifying the district as a destination for healthcare excellence long into the future.

Hale House is a pioneering development designed to drive healthcare transformation through collaboration, forward-thinking innovation and the integration of the latest technologies.

Located on Portland Place in the heart of Marylebone, Hale House spans three buildings: 19 Portland Place, 76-78 Portland Place (now open), and 42 Portland Place (opening June 2025).

The development is poised to become the London’s foremost destination for HealthTech startups, investors, and healthcare pioneers.

A Hub for HealthTech Innovation

The Harley Street Health District represents 40 per cent of London’s independent healthcare market and 10 per cent of the UK market.

With a focus on advancing emerging technologies, groundbreaking research, and expanding services across the entire healthcare pathway, Howard de Walden is committed to fostering collaboration and innovation.

 Mark Kildea, Chief Executive of The Howard de Walden Estate, commented: By investing in health innovation, we have created spaces that will push the boundaries of emerging technologies and help those involved in ground-breaking research, in a location known for leading healthcare, innovation, influential policy think tanks and investors.”

The district is home to world-class healthcare providers, including HCA, Cleveland Clinic, Mayo Clinic, and Cedars-Sinai, along with leading UK institutions such as The Royal Marsden, Guy’s and St Thomas’, UCLH, and Moorfields.

Accelerating HealthTech Collaboration

Hale House provides a range of flexible workspaces—from private offices and coworking areas to meeting rooms and event spaces—all designed to promote collaboration among HealthTech innovators.

The development offers a wide array of state-of-the-art amenities, including media production facilities, a wellness room, and a rooftop garden terrace.

The hub is set to accelerate HealthTech innovation by connecting startups to a dynamic ecosystem of over 2,500 healthcare professionals, cutting-edge testing facilities, and key industry leaders through exclusive networking events.

“We are confident that Hale House will play a pivotal role in driving the transformation of healthcare,” said Kildea.

Hale House has already secured significant partnerships, including UCLPartners, one of the world’s largest academic health science organisations; The NHS Innovation Accelerator, a national fellowship programme supporting innovators to scale and One HealthTech, a volunteer-led, global community of health innovators which champions diversity and inclusion.

Highlighting Hale House’s commitment to fostering a strong, inclusive and interconnected community for HealthTech businesses.

Dr Chris Laing, CEO, UCLPartners said: “Our new home at Hale House will help us connect the health technology and life science sectors with healthcare providers, patients and the public.

“This will be invaluable to our work delivering novel solutions to challenges in health and care and driving economic growth.

We look forward to welcoming and supporting innovators both near and far to benefit from the world-class health ecosystem on our doorstep. Together we can develop novel solutions that will define the healthcare of the future.”

Maxine Mackintosh & Angela Maragna, Co-Directors, One HealthTech, added: “We’re so pleased to be partnering with the team at Hale House; it’s rare to find a space and people who truly understand the power of community-led energy, the importance of diverse voices, and the creativity sparked when you bring together all parts of the health innovation world.

“We’re excited about what this partnership can achieve and can’t wait to see it thrive.”

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Femtech World reveals startup of the year shortlist

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We are excited unveil the three finalists competing for one of the Femtech World Awards’ most coveted honours: the Startup of the Year Award, sponsored by Future Fertility.

This award celebrates an early-stage company making a bold impact in women’s health through innovation, vision and execution.

The winner will be announced at our virtual ceremony on 19 June, with the decision made by a representative from category sponsor Future Fertility.

Congratulations to the shortlist and thank you to everyone who entered or nominated.

Startup of the Year Shortlist

Hello Inside is the first women’s health AI company to turn daily metabolic signals into outcomes women feel and healthcare systems reimburse.

Women’s health has long been under-researched, and current AI benchmarks fail on women’s health questions roughly sixty percent of the time.

Hello Inside built the architecture to close that gap.

Across four years and 12,000+ validated metabolic profiles, three in four women improve at least one symptom within ninety days.

They lose four kilograms in three months, moving from overweight into the healthy range. In a clinical study with Alisa Vitti’s Flo Living, 91.9 per cent reduced PMS burden within sixty days.

OvartiX is doing something that has never been done before: building a drug discovery engine purpose-built for women’s health.
Its lead programme, OVX001, targets medically induced menopause – a condition affecting young female cancer patients who undergo chemotherapy or radiotherapy.
These women are cured of cancer but enter menopause overnight.
There is currently no approved drug to prevent it. OVX001 is designed to change that, preserving 80–95 per cent of ovarian follicles during treatment without compromising anti-tumour efficacy.
Behind the science is the OmiXX platform: the first ML-driven drug discovery tool built specifically for female physiology, using proprietary ovarian cellular models and human multi-omics data.

U-Ploid is an early-stage biotechnology company tackling one of the most fundamental challenges in fertility care: the sharp, age-related decline in egg quality that limits outcomes across IVF and egg freezing.

While much of the field focuses on improving assessment and selection, U-Ploid is developing a first-in-class therapeutic approach designed to improve egg quality itself by addressing the biological causes of age-related chromosomal errors.

Supported by strong preclinical evidence and now advancing into human studies, U-Ploid combines scientific rigour, regulatory discipline and long-term vision to help redefine what is possible in fertility care.

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Gestational diabetes increases risk of type 2 diabetes – even at normal weight, study finds

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Gestational diabetes is a strong risk factor for future type 2 diabetes, even in women with normal pre-pregnancy weight, according to a study at the University of Gothenburg.

The researchers call for earlier testing and better follow-up.

“Our results show that gestational diabetes functions as a kind of stress test for the body’s ability to manage blood sugar, and identifies women with a greatly increased risk of future type 2 diabetes”, said Jon Edqvist, PhD and affiliated to research at the University of Gothenburg, and operating room nurse at Sahlgrenska University Hospital.

Gestational diabetes is a special type of diabetes that can affect pregnant women.

The condition is defined as elevated blood sugar levels, without previously known diabetes. Treatment involves self-monitoring of blood sugar, advice on lifestyle habits and, if necessary, medication.

Identifying gestational diabetes is important because the disease increases the risk of complications such as preeclampsia, the need for a cesarean section and high birth weight for the baby.

Those who have had gestational diabetes are also at higher risk of later developing type 2 diabetes.

In the current study, published in eClinicalMedicine, researchers now show that gestational diabetes is a strong indicator of future risk of developing type 2 diabetes, even in women with normal weight before pregnancy.

Elevated risk even with normal weight

The study is based on data from the Medical Birth Registry on just over 1.15 million first-time mothers in Sweden, who gave birth between 1987 and 2019. 16,870 women with confirmed gestational diabetes were compared with age-matched women without the diagnosis. The median follow-up period was nine years.

The results show that women with a BMI of 35 and above, i.e. severe obesity, had an almost tenfold increased risk of developing gestational diabetes compared to women with normal weight.

The risk of subsequent type 2 diabetes also increased with higher BMI, but it was significantly increased even with normal weight, which the researchers describe as particularly worrying.

More follow-up and more studies

The researchers behind the study welcome the recently updated recommendations on gestational diabetes in Sweden, where a higher proportion of pregnant women at increased risk are expected to be offered testing earlier in pregnancy, and if necessary, interventions.

“Diagnostics and care of gestational diabetes have looked very different in different parts of the country,” said Annika Rosengren, professor at the University of Gothenburg.

“There is a need for both improved follow-up after gestational diabetes, and more studies that investigate how such follow-up affects future health and prognosis”

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The invisible infrastructure of patient safety and why digital governance matters

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By Misbah Mahmood, CXIO & Clinical Safety Officer, Bradford District Care Trust, (Former digital midwife at Leeds Teaching Hospitals and long-standing K2/HHA customer and collaborator)

Across the NHS, digital governance is frequently misunderstood.

It is often seen as a bureaucratic necessity or a technical, administrative process that becomes invisible once a system goes live or as a barrier to innovation when services are under pressure to change quickly.

However, digital systems do far more than document care. They shape how care is delivered, how risk is identified and interpreted, and how clinical decisions are made.

When systems are well designed and well governed, they support clinical judgement and safe practice.

When they are not, the impact is felt directly at the bedside, as illustrated by recent concerns over an AI discharge summary tool trialled at Chelsea and Westminster.

Here, unresolved questions about regulatory status and assurance exposed the consequences of deploying clinically influential technology without sufficient clarity or oversight.

In maternity services in particular, care is complex, unpredictable, and deeply dependent on context. Rapid decision making and information continuity across settings are essential.

As digital systems increasingly influence day-to-day practice, the way they are designed, governed, and used can either reinforce safe care or quietly undermine it.

Digital governance distinguishes technology that protects women and babies from technology that introduces hidden risk.

The myth of “invisible infrastructure”

When people hear the word “governance”, they often think of forms, meetings and compliance. For clinicians, it can feel like a tick box exercise that sits in the way of getting things done.

But governance decisions show up at the most critical moments of care, often without being named as such.

As clinicians, we instinctively understand safety in physical terms. If a blood pressure machine stops working, that’s immediately recognised as a patient safety issue. It gets escalated, reported and fixed.

But for a long time, digital issues have not been treated the same way. Slow systems, unreliable access, or inability to view the EPR were often accepted as “just one of those things”. Yet the impact on safety can be just as significant.

If you can’t see the record, you can’t see the risks. If you can’t trust the system, you start working around it.

Electronic patient records are no longer passive repositories of information. They influence what clinicians notice, how quickly they escalate concerns and what decisions they make.

That means the way these systems are governed, and how they are designed, tested and introduced, has direct consequences for patient safety.

A good example of this is central foetal monitoring. Used well, it can support situational awareness. But without clear governance and shared understanding, it can also create a false sense of security.

Being explicit that central monitoring does not replace bedside assessment or escalation is essential. If staff assume “someone else is watching”, the technology has unintentionally weakened safety.

Why safe digital infrastructure matters more than ever in maternity

Maternity care is non‑linear. Risk changes rapidly, and plans change, as women move between community and hospital settings.

Many digital systems are built around rigid templates and linear workflows that do not reflect this reality. When systems don’t fit practice, practice adapts.

Parallel notes, paper diaries, and reliance on free text are not resistance to digital tools; they are practical responses to keep care safe.

Operational realities add further challenge. Community midwives work across geography with unreliable connectivity, making offline access a safety requirement rather than a technical convenience.

Systems that support secure offline working reduce rushed documentation and missed safety checks.

Misbah Mahmood

On the labour ward, pressures intensify. Emergencies escalate quickly and staff are often fatigued. Here, usability becomes inseparable from safety.

Systems that add unnecessary steps increase cognitive load precisely when attention must remain on the patient. At four in the morning, design can either support safe decision‑making or work against it.

When the safest decision is saying “not now”

Digital governance is as much about preventing unsafe change as enabling innovation. Not every system that is technically ready is clinically ready.

Introducing change during periods of strain, limited training, or inadequate testing increases risk.

Pausing a rollout is rarely comfortable as delivery pressures create momentum to proceed. Effective governance, however, gives organisations permission to prioritise safety over speed.

Delaying implementation to allow further testing or clinical engagement often leads to safer adoption and greater staff trust.

Saying “not now” is not resistance to change. It is a mature safety response, as introducing change at the wrong time can cause harm that is far harder to undo.

Codesign, not configuration: new models for supplier partnerships

Safe digital transformation depends on genuine partnership between NHS teams and suppliers, with shared responsibility for clinical risk.

 Effective collaboration starts early, with meaningful clinical involvement, transparency about system constraints, and shared understanding of risk.

It continues through testing in real clinical environments and shared accountability for safety outcomes after go‑live.

Working with Harris Health Alliance and the K2 maternity tool made these conversations more effective.

Responsiveness to safety feedback was faster, and small design changes, such as surfacing critical risk information or adding validation checks to reduce error under fatigue, had significant impact on usability and safety.

Every change, however minor it appears, is a clinical safety decision. Digital governance provides the structure to recognise this and ensure changes are designed and implemented accordingly.

People, process and technology are an interdependent system

Technology does not fail in isolation. Risk emerges when people, processes, and digital systems are misaligned. Even the most sophisticated EPR will struggle if staff are unsupported, processes have not evolved, or workflows do not reflect clinical reality.

Technology can also obscure risk by embedding unsafe or outdated practices into systems that appear efficient when governance focuses only on technical delivery.

Effective digital governance recognises that patient safety depends on the interaction between people, processes, and technology.

Skills, confidence, and behaviours matter, as do evidence‑based, consistent processes and systems that are usable, reliable, and aligned with real clinical work.

Safety improves when these elements are deliberately aligned and governance focuses on learning rather than blame.

Design matters and systems must be fast, predictable, and forgiving of human fatigue. The same principle is evident in data quality.

A yes/no field relating to cord prolapse produced alarming figures due to human factors rather than practice.

Introducing a simple validation check prompting confirmation improved data quality and reduced risk by addressing system design, not individual behaviour.

This is digital governance in practice. It is recognising where design and reality collide and fixing the system rather than blaming clinicians.

From invisible to essential 

Digital governance should no longer be invisible. It must be recognised, valued, and treated as a core component of patient safety.

That means involving clinical safety expertise from the outset, listening to frontline concerns, designing for real-world conditions, and being willing to pause when something does not feel safe.

The absence of incidents does not mean the absence of risk; often, it means the system has not yet failed under the wrong circumstances.

Maternity services, with their complexity and sensitivity, have much to teach the wider NHS about safe digital transformation.

When governance is shared, practical, and grounded in real clinical experience, digital systems can genuinely support safer care and not just record it.

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