News
Interview: Phantom uterus aims to revolutionise gynaecological procedures

A biomedical engineer is tackling the painful reality of gynaecological procedures, with a “phantom uterus” that offers a safe, anatomically accurate platform for designing and testing medical devices, with the potential to transform comfort, safety and innovation in women’s healthcare.
Women-specific medical devices have received little attention in science and medical research, resulting in few advancements for decades. Routine procedures such as the insertion of the contraceptive implant often leave women in severe pain or cause them to avoid it altogether.
Almost 90 per cent of women report moderate to severe pain during a cervical procedure for IUD insertion, with 18 per cent using an alternative to IUD for contraception because of fear of how painful they can be.
Biomedical engineer, Saskia Hale, has designed and manufactured a life-sized phantom of a pre-menopausal non-pregnant uterus for the planning and designing of implants.
Long term, the innovation has the potential to improve the design, functionality and safety of medical devices used in gynaecological procedures, by providing an anatomically and mechanically accurate model.
A recent graduate of Biomedical Engineering from Imperial College London, Hale developed the
device as part of her Master’s Project.
It integrates advanced medical imaging, computational modelling, and materials science, enabling safe and effective gynaecological device development and reducing the need for live patient trials.
Developing the phantom uterus
Hale, who says she is passionate about improving the quality of people’s lives, is currently a biomedical engineer with Arete Medical Technologies.
Her idea for the phantom uterus came about after Charing Cross Hospital’s clinical engineering department began developing a device to test the geometry of a mechanically accurate uterus.
“I had an initial meeting with my supervisor, Dr Warren Macdonald, and the hospital to understand more of the specifics and what they wanted from the project to make it meaningful for them,” Hale tells Femtech World.
“I began to learn more about the materials that could replicate the uterus structures. One of the most interesting ways of doing this was not just by looking at journals, but by visiting the hospital’s Cadaver Lab and speaking to anatomy prosectors.
“I took away some great points, regarding not just the uterus, but considering how it interacts with the surrounding organs.
“Early in the design process, I also realised the importance of making the model adaptable to different uterine positions, not just the anteverted position, the most common type. It was really important to me that everyone was represented to improve the experience women have with intrauterine medical devices.”
How it works
The phantom uterus was developed through extensive research to help Hale understand the anatomy of the uterus – segmenting medical images to create a 3D model and exploring the viability of potential materials before the phantom uterus was manufactured and tested.
“The phantom uterus I developed is a model to allow for deployment planning and geometric designing of an implant,” says Hale.
“It works free-standing at the moment, but in the future, I hope to add a pelvis and the surrounding organs as I look towards improvements and the realism of the phantom uterus.
Hale adds, “Any device that can be inserted vaginally into the uterus can be tested to see how it interacts.”
Two key areas of the uterus needed to be validated for the design.
“After careful material selection, which influenced the manufacturing technique, anatomical validation and medical device validation were needed,” Hale explains.
“The anatomical validation showed that the uterus developed was a little bit smaller than expected, possibly due to the scans used and the shrinkage during moulding, needing to be larger than what was accounted for.
“The medical device validation study looked at a speculum being inserted into the phantom uterus and the key things a physician would do, see and feel, and how closely they were mimicked by the uterus. The results showed an 80 per cent performance score, and with some improvements, that score is expected to only go up.”
Supporting unmet need
Women-specific medical devices, such as contraceptive devices, are underfunded and under-researched, Hale highlights, emphasising that the phantom uterus allows for precise testing and optimisation of devices, ensuring they are safe, effective and comfortable for patients.
“A phantom uterus would also address the underfunding in women’s health that has resulted
in gaps in knowledge and treatment options, as a safer method for pre-clinical trials and the redevelopment of devices that may not work effectively,” says Hale, who shared her research at BioMedEng24.
“I’d love to continue furthering the work on the phantom uterus and to share my research so others can learn and progress in medical device design within women’s health.”
Earlier this year, Hale was selected as the winner of the Judge’s Choice Award at the Femtech Awards 2025 for her work on the phantom uterus project, an achievement she describes as a “complete surprise” and “an absolute privilege”.
“This is my life mission,” says Hale. “Being recognised alongside such influential individuals and organisations in the femtech field is incredibly meaningful, especially since I am so early on in my career.”
She adds: “This achievement wouldn’t have been possible without the support of Imperial College London and Charing Cross Hospital, especially my supervisor, Dr. Warren Macdonald, as well as Joelle and Aheed from Charing Cross.”
Insight
UK reviews surrogacy firm over rejected insurance claims

The UK government is reviewing a surrogacy firm after complaints that medical insurance claims involving surrogates in Mexico were rejected.
The Department of Health and Social Care (DHSC) is considering whether UK-based provider My Surrogacy Journey should remain listed on gov.uk as one of four domestic surrogacy agencies available to intended parents.
The review follows allegations concerning its Mexican sister company, where surrogates are based.
Health minister Diana Johnson said: “The department is looking into the allegations about My Surrogacy Journey.
“As part of that assessment, the department will consider whether it is appropriate for that company to remain on the gov.uk list of agencies.”
Emails sent by My Surrogacy Journey chief executive Michael Johnson-Ellis and seen by the Guardian suggest multiple surrogate women in Mexico had their insurance claims rejected.
The emails also suggest 300 couples using the company were moved to a new insurance provider because of the increased risk of claims being rejected.
Commercial surrogacy is banned in the UK, where only altruistic arrangements are permitted.
My Surrogacy Journey operates a not-for-profit UK branch alongside for-profit sister companies in Mexico and the US. All three companies have the same owners and chief executives.
The reported insurance issues relate to surrogacy arrangements in Mexico.
One couple told the Guardian they paid tens of thousands of pounds to cover medical costs after their surrogate had a hysterectomy during childbirth and an insurance claim was refused.
The Guardian said it understood that at least five sets of parents said they had to cover medical costs after insurance claims were rejected.
In an email to the couple whose surrogate underwent a hysterectomy, Johnson-Ellis wrote: “We have already told you that the insurance companies have been declining some of the claims and we are actively working with the broker to get this issue resolved but you should also consider that they may not be paid out and there is nothing we are able to do to change this …
“We appreciate this is not an insignificant sum but this genuinely is out of our control.”
Johnson-Ellis also said the company had switched insurance providers, writing: “We’re also managing this for 300 other journeys, which is a complex position to be in.”
Lawyers acting for My Surrogacy Journey said the company did not comment on individual cases, but that existing insurance policies were in place and claims continued to be accepted and processed.
They said the company understood that a small number of claims had been rejected and was supporting people seeking to resolve those claims with an insurer.
Under the surrogacy arrangements, intended parents are understood to be contractually required to cover medical costs not paid by an insurer.
The couple said they had been recommended the company’s Mexico option. Its website advertises that intended parents using the route can have a baby in “under 18 months”.
They said they were told the UK route could take up to five years and that the US option was much more expensive.
Lawyers for My Surrogacy Journey said prospective parents are given information about typical timelines, costs, legal frameworks and practical considerations, and that the 18-month timeframe is indicative only.
The couple said their surrogate developed placenta accreta, a serious condition in which the placenta attaches to the wall of the uterus.
Emails from Johnson-Ellis acknowledged that the insurance provider investigated the birth after the surrogate experienced health complications.
The parents are considering legal action, while the Guardian said it understood at least four other couples were reviewing their options.
Phil Brickell, MP for Bolton West, raised concerns in parliament about a separate couple who had used My Surrogacy Journey.
He said: “Two of my constituents recently travelled to Mexico, where their children were born by surrogacy.
“Those births were facilitated by a company called My Surrogacy Journey, which is listed on gov.uk.
“While in Mexico, they had repeated traumatic experiences with the company relating to issues including insurance for their children, accusations of bullying towards staff and repeated efforts to silence any constructive criticism.
“I understand that other members of this house have received similar complaints.”
Brickell called for My Surrogacy Journey to be removed from gov.uk pending a review by the Human Fertilisation and Embryology Authority.
Lawyers acting for My Surrogacy Journey said the company was communicating with DHSC and was confident any issues could be resolved.
News
‘Limited scientific evidence’ for most menopause supplements, expert says

Many menopause supplements contain ingredients with limited evidence for symptom relief, while formulations and prices vary widely, a study has found.
Researchers analysed 201 products sold by nine major UK retailers, comparing their ingredients, doses and monthly costs.
Prices ranged from £1.50 to £95 a month, while no single ingredient or category of ingredient was common across all products.
The study, carried out by University College London, found that 80 per cent of products contained herbs, 77 per cent contained vitamins and 74 per cent contained phytoestrogens, naturally occurring plant compounds found in foods including soy and flaxseed.
Vitamin B6 was the most common vitamin, while red clover and sage were the most frequently identified plant ingredients.
Researchers said more evidence was needed on the effectiveness and safety of supplements marketed for menopause symptoms.
Professor Joyce Harper, senior author of the study and professor of reproductive science at University College London, said: “The menopause supplement market is growing rapidly, despite limited scientific evidence that many of these products improve menopause symptoms.
“Some social media influencers promote these products as effective solutions, despite many claims not being supported by scientific evidence.
“This can contribute to the spread of misinformation and help drive a rapidly growing menopause supplement market, leading some women to spend substantial amounts of money on supplements in the hope of improving their symptoms and overall wellbeing.”
Half of the supplements did not contain vitamin D, while less than 24 per cent contained calcium.
The British Menopause Society and International Menopause Society have highlighted vitamin D and calcium as important for maintaining bone health and preventing osteoporosis after menopause.
Researchers also identified botanical ingredients that may carry risks, including black cohosh.
Poppy Sullivan, first author of the study, said: “Certain botanical ingredients in some menopause supplements may also have risks.
“Black cohosh, in particular, is known to carry a potential risk of liver toxicity.”
The amounts of vitamins and minerals included in different products also varied widely.
Sullivan said: “Some nutrients can have adverse effects when consumed in excess over time.
“For example, excessive vitamin D intake can theoretically lead to high calcium levels, which could cause adverse effects such as vomiting and confusion.”
The study found little empirical evidence supporting the effectiveness of even the most expensive products.
Researchers called for more high-quality research, including clinical trials, to determine whether menopause supplement ingredients are effective and safe.
They said the findings could also help healthcare professionals understand the wide variation in supplement formulations.
The researchers acknowledged that the analysis may not have included every menopause supplement available in the UK.
Pregnancy
Ultrasound Direct extends Trice Imaging partnership

Ultrasound Direct has extended its Trice Imaging partnership for three years, adding a reporting tool across its 70-clinic UK network.
The private ultrasound provider will continue using the Tricefy platform for secure image storage and patient engagement, alongside TriceIQ for efficiency and productivity analytics.
It will also introduce Trice Workspace Reporting across its network. The companies say the tool will help standardise ultrasound reporting templates and workflows and reduce variation between clinics.
Ultrasound Direct carries out an estimated 120,000 patient scans each year across services including pregnancy, fertility, women’s health, men’s health and other diagnostic pathways.
Its network uses a large pool of sonographers working across different ultrasound systems and serves referral routes including self-referring patients, GPs and commercial partners.
Mike Steward, founding director at Ultrasound Direct, said: “Having worked with Trice Imaging since 2018, we first partnered to replace manual methods of providing scan images to expectant parents with Trice’s secure electronic image-sharing platform. Today, every study performed across the Ultrasound Direct Network is recorded and stored on Tricefy, while our clinical services have expanded considerably beyond pregnancy into fertility, women’s health, men’s health and other diagnostic pathways.”
He added: “To continue futureproofing our image management strategy across a network of 70 clinics, a large team of sonographers, varying ultrasound systems and a growing number of referral partners with different needs, we decided to extend with Trice Imaging. This includes the introduction of the new Trice Workspace Reporting module to help us scale and standardise our ultrasound reporting templates and workflow, reducing variability between clinics.”
The partnership began in 2018, initially focusing on replacing manual methods of sharing pregnancy scan images with expectant parents.
Johanna Wollert Melin, founder and chief executive of Trice Imaging Europe, said: “Ultrasound Direct has been a valued partner in the UK for 8 years.”
She added: “At the heart of the relationship is a willingness to explore new ideas, test new tools and the spirit to solve real challenges across a large and complex clinical network.”
Mark A. Samii, chief revenue officer at Trice Imaging, said: “We are delighted to retain and extend our relationship with Ultrasound Direct.”
He added: “The addition of Trice Workspace Reporting addresses a challenge we hear from multi-site providers globally – keeping reporting quality consistent across many users, systems, referral or payer relationships.”
Steward said Ultrasound Direct continues to see growing demand for private diagnostics alongside NHS care from self-referring patients and an increasingly diverse range of professional and commercial referral partners.
He added: “As that development continues, scalable digital infrastructure becomes increasingly important. Our focus is on ensuring that a growing national network can support consistent clinical workflows, different referral pathways and the technology requirements of the future, while continuing to provide patients with accessible diagnostic services.”
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