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Connect with regulatory affairs consultancies specializing in this region.
Registrar Corp
維吉尼亞州漢普頓 (總部), 中國深圳, 英國倫敦, 法國巴黎, 西班牙馬德里, 印度海得拉巴, 馬來西亞吉隆坡, 以色列特拉維夫, 瓜地馬拉瓜地馬拉市, 南非開普敦
000 家企業處理 FDA 註冊、美國代理人要求、標籤合規及扣留協助等事務。我們提供包含 FDA 合規監控器 (Compliance Monitor) 和不良事件管理軟體在內的技術解決方案,協助食品、飲料、醫療器材、藥品和化妝品行業的企業應對複雜的法規環境。
MedEnvoy Global
荷蘭海牙, 英國倫敦, 美國, 瑞士, 澳洲
一家全球法規合規合作夥伴,專注於為醫療器材和 IVD 製造商提供在地代表(EC Rep、UKRP、CH Rep、美國代理人)和獨立進口商服務。我們協助企業應對歐洲、英國、瑞士和美國的複雜法規,同時保持供應鏈的靈活性。
KoBridge Co Ltd
韓國首爾, 瑞士洛桑
我們為需要應對日益複雜的全球法規的醫療器材製造商提供快速、有效和靈活的解決方案。他們的核心能力涵蓋 CE 標誌、FDA 510(k)/PMA、MDSAP,尤其是韓國 MFDS 註冊和 KGMP 合規性。他們處理主動、非主動、組合和動物源性設備,提供從策略規劃和文件準備到品質系統實施 (ISO 13485) 和稽核的服務。
IMed Consultancy Ltd
英國, 愛爾蘭
幫助醫療器械和體外診斷公司進行 CE 標記、品質管理系統、審計和全球註冊。
March 15, 2025
Approximately 5 minutes
Accelerating Access to Transformative Medicines: The UK’s ILAP
Accelerating Access to Transformative Medicines: The UK’s ILAP
1. What is the ILAP
The Innovative Licensing and Access Pathway (ILAP) is a UK initiative led by the Medicines and Healthcare products Regulatory Agency (MHRA), designed to accelerate the time it takes for transformative new medicines and drug-device combinations to reach patients within the National Health Service (NHS). It provides a single integrated platform for sustained collaborative working between developers, regulators, health technology assessment (HTA) bodies and the NHS.
Source: Innovative Licensing and Access Pathway (ILAP) - GOV.UK
Unique in the world, ILAP is the only end-to-end access pathway where a developer can work collaboratively with the national health system, regulators and HTA bodies from the earliest stages of clinical development, enabling a system-wide approach to product development and access.
Source: Innovative Licensing and Access Pathway (ILAP) - GOV.UK
2. Goals and purpose
The ILAP aims to:
- Reduce timelines for research, regulatory approval, HTA evaluation and adoption into standard care.
- Provide coordinated support across regulatory, clinical and health system stakeholders.
- Align evidential requirements so developers can plan and generate data efficiently.
- Facilitate earlier engagement with NHS stakeholders and patients to support adoption and system readiness.
Source: Innovative Licensing and Access Pathway (ILAP) - GOV.UK
3. Entry into the ILAP: Innovation Passport
The first step for a product to join the ILAP is applying for an Innovation Passport. This designation is awarded to developers whose products meet defined eligibility and selection criteria, which typically include:
- A therapeutic aim and evidence of safe use in humans, and
- Clinical development where confirmatory trials have not yet started.
Source: Innovative Licensing and Access Pathway (ILAP) application guidance - GOV.UK
Once an Innovation Passport is granted, the developer works with ILAP partners to create a Target Development Profile (TDP) — a collaborative roadmap outlining key evidence generation and regulatory milestones throughout development.
Source: Innovative Licensing and Access Pathway (ILAP) - GOV.UK
4. Collaboration and services offered
The ILAP brings together multiple partners, including:
- MHRA – the UK medicines regulator
- NHS – ensuring healthcare system readiness and adoption
- HTA bodies, such as NICE (National Institute for Health and Care Excellence), SMC (Scottish Medicines Consortium) and AWTTC (All Wales Therapeutics and Toxicology Centre)
Source: Innovative Licensing and Access Pathway (ILAP) - GOV.UK
Collaboration through the ILAP includes early and ongoing interactions with stakeholders, priority access to regulatory and HTA processes, and coordinated guidance to support the generation of evidence needed for licensing and adoption.
Source: Innovative Licensing and Access Pathway (ILAP) - GOV.UK
5. Benefits for developers
Developers participating in the ILAP can benefit from:
- Faster timelines, by aligning regulatory and HTA activities in parallel.
- De-risked development, via early insights into evidence requirements.
- Improved predictability, through coordinated planning and regular engagement.
- Early patient and NHS involvement, enhancing the likelihood of successful adoption into clinical practice.
Source: Innovative Licensing and Access Pathway (ILAP) - GOV.UK
6. Scope of eligible products
The ILAP is open to both commercial and non-commercial developers (UK based or global) of transformative medicines and drug-device combinations with a therapeutic goal, provided preliminary human safety data exist and confirmatory trials are not yet initiated.
Source: Innovative Licensing and Access Pathway (ILAP) - GOV.UK
7. Real-world uptake
Since the refreshed ILAP launched in 2025, several investigational products have been awarded Innovation Passports and enrolled in the pathway, demonstrating the real-world application of this collaborative model to accelerate access for promising therapies, including those for rare or unmet medical needs.
Source: The new Innovative Licensing and Access Pathway welcomes first investigational products
Summary: The ILAP represents a world-leading, integrated, end-to-end pathway that aligns regulators, HTA bodies, healthcare providers and developers to accelerate the journey from innovation to patient access, especially for transformative therapies addressing significant unmet medical needs.
Source: Innovative Licensing and Access Pathway (ILAP) - GOV.UK
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