Consent is one of the most critical moments in the patient journey, influencing both patient safety and the quality of care. Yet many healthcare organisations still rely on paper-based processes, which can create delays, variation, and unnecessary risk. These systems often lead to missing or incomplete records, inconsistent information provision, and materials that are no longer up to date. This is especially important in a post-Montgomery environment, where consent is no longer a tick-box exercise, but instead requires clear, consistent information and patient understanding at every stage.

Digital consent offers a more robust and efficient approach, but its effectiveness depends on the quality of information patients receive. Digital consent must be supported by clear, trusted, and accessible patient information, to enable shared decision-making, reduce medicolegal risk, improve patient safety, and free up time for clinical teams.

Why Informed Consent is Vital Within Healthcare

When patients are not given clear, detailed information about their treatment, or when consent processes are poorly evidenced, healthcare organisations can face significant financial and operational pressure.

Whilst the organisational impact of inadequate consent is important, the implications for patient safety and individual outcomes are just as significant. Inconsistent consent practices can affect patient understanding and preparedness for care, potentially leading to avoidable distress and harm.

An increase in patient safety concerns can also undermine patient confidence and, over time, affect organisational reputation. These issues are rarely brought upon by a single failure but emerge from processes that lack consistency, transparency or oversight.

This highlights a key principle that consent and patient information must work together. Clear, trusted patient information underpins informed decision-making, while standardised, regulatory aligned consent processes provide the assurance organisations need. Together, they support a patient centred approach that reduces risk, supports clinicians and strengthens confidence in care.

Radar Healthcare Digital Consent: Strengthening Patient Safety, Governance and Efficiency

Digital consent is increasingly being used to reduce variation and risk within consent processes, while also improving efficiency for clinical teams. Moving away from paper-based workflows enables organisations to provide patients with clear, accurate and up-to-date information that supports patient safety and reduces medicolegal risk.

Through standardised, procedure specific workflows, digital consent helps strengthen patient safety and quality of care by ensuring information is consistent across teams. This helps to reduces variation in how risks, benefits and alternatives are communicated and contributes to minimising misunderstanding, while also addressing common issues associated with traditional processes, such as illegible handwriting, incomplete records and reliance on outdated forms.

Designed with patients at the centre, Radar Healthcare Digital Consent is a consistent approach that supports clearer, safer conversations between clinicians and patients. The use of accessible formats including video, animation, Easy Read and multi‑language content decreases communication barriers and supports patient understanding, enabling individuals to make informed decisions about their care and contributing to safer care outcomes. Accessibility in consent isn’t optional; it is a legal and ethical duty.

Radar Healthcare Digital Consent helps improve governance and compliance processes by ensuring the right information is documented and accessible. Clear audit trails of patient engagement make it easier to evidence shared decision-making and demonstrate alignment with professional and regulatory expectations. This level of consistency is particularly important when organisations need to respond quickly and confidently to scrutiny or challenge.

Digital consent can also ease operational pressures, as it enables patients to review information and complete elements of the consent process in advance from their home. This helps reduce administrative burden on staff, minimise delays or cancellations, and allows clinical teams to focus on patient care and those they care for.

However, even the most robust digital consent processes rely on patients having access to clear, trusted information. Without this, it becomes difficult to ensure that consent is truly informed, highlighting the role that high-quality patient information plays within the consent process.

EIDO Patient Information: The Foundation of Informed Consent

For consent to be truly informed, patients must have access to high-quality information that they can understand and trust. While digital consent helps standardise and evidence the consent process, it is the information provided to patients that enables them to make meaningful, informed decisions about their care.

In a post Montgomery environment, the emphasis is no longer on whether consent has been recorded, but whether patients were supported with clear, balanced and relevant information about risks, benefits and alternatives. Without this foundation, even well-designed consent processes remain vulnerable to challenge.

Becoming part of Radar Healthcare last year, EIDO Patient Information supports this by providing trusted, standardised patient information designed to improve understanding and reduce inconsistency in how information is communicated across clinicians and services. EIDO Patient Information is developed with clinicians through a ten step process, ensuring it is relevant and evidence based and is also regularly reviewed. This approach helps address the risks associated with outdated materials or individual interpretation, while supporting clearer, more meaningful conversations between patients and clinicians.

“These [EIDO] documents are now, technically speaking, our best defence to consent claims.” – Legal Services Manager – NHS Trust

EIDO Patient Information has been endorsed by Royal Colleges and patient safety bodies and has also been referenced within case law. It is the only provider to have been explicitly acknowledged by the High Court as authoritative in a consent related case (Biggadike v El Farra). This further underlines the importance of providing patients with high-quality, assured information as part of the consent process.

Importantly, the impact of high-quality patient information is measurable, with evidence showing that 28% of organisations using EIDO Patient Information pay out less in consent related litigation.

Building Safer Consent Through Trusted Patient Information

Informed consent is no longer defined by a single moment or a signed form, but by the quality, consistency and transparency of the process that supports it. As expectations around consent continue to evolve, healthcare organisations must be confident not only that it has been recorded, but that patients were genuinely informed and supported to make decisions about their care.

Digital consent offers an important opportunity to bring greater structure, consistency and assurance to consent processes, while high quality patient information ensures those processes are truly informed. By connecting trusted patient information with governed digital consent workflows, healthcare providers can move away from fragmented approaches and towards a more patient centred, reliable model of consent, reducing medicolegal risk, improving patient understanding and strengthening patient safety, w...

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