Where energy meets experience
Navigate the complex pathway to patients with ease
Who we are
We are a team of bold, dynamic thinkers with deep expertise in pharmaceutical market access, regulatory affairs, medical and scientific strategy, and public policy. Rooted in local expertise and driven by global collaboration, we empower health technology developers to deliver impactful therapies to patients across Europe.
Our approach combines agility with precision, guiding you through the complexities of European patient access with confidence and clarity.
Explore your journey
01
Phase I
Build confidence with compliant, scalable early regulatory and clinical trial strategies.
02
Phase II-III
Generate evidence that aligns with payer needs and drives impact.
03
Registration
Achieve first-time regulatory and HTA approval with aligned submissions and proactive planning.
04
Post-launch
Sustain long-term market access and impact with strategic post-launch support.
EPRI - EndPoint Result Interpreter
EPRI (EndPoint Result Interpreter) is a cutting-edge, user-friendly AI solution designed to streamline the creation of tailored, high-quality German AMNOG, UK NICE and EU Joint Clinical Assessment (JCA) dossiers. Our innovative technology helps to manage complexity, reduce time and costs and ensure the highest standards of accuracy and reliability.
Our expertise:
Strategic Advisory
We are your partner in overcoming the complexities of European markets, offering customised solutions to guide you seamlessly through every step of the patient access journey from development and registration through access and launch preparedness.
National Market Access Strategy & Negotiation
Your path to success begins with a clear, well-defined strategy. At Kintiga, we combine local insights with therapeutic expertise to unlock Europe’s healthcare markets.
EU HTA
Our European team expertly navigates the complexities of EU HTA procedures, providing both strategic guidance & comprehensive end-to-end support for JSCs & JCAs at every stage of the process. We are committed to ensuring your products reach patients across Europe efficiently & effectively.
Pricing Strategy
Our experts start with what matters most to access stakeholders and work backwards to develop robust pricing and reimbursement strategies tailored to each market to reflect the value for your product.
Value Communication & Stakeholder Management
We transform complex evidence into compelling, compliant narratives. Through evidence-based storytelling and stakeholder input, we help your product achieve its full potential across diverse markets.
HEOR & Modelling
At Kintiga our expertise in modelling data, outcomes, and costs provides stakeholders with clarity to fully understand the value of treatments, which is vital for healthcare decision making.
Our products
Navigate evolving regulations and market demands confidently with up-to-date insights and guidance from Kintiga’s innovative AI-powered digital tools.
Hive by Kintiga
Access the collective expertise of our consultants and the insights and strategic guidance to simplify approvals across Europe’s healthcare any time and from anywhere.
EPRI
EPRI (EndPoint Result Interpreter) is a cutting-edge AI solution designed to streamline the creation of tailored, high-quality dossiers.
Our experience
Delivering a Successful SMC Re‑Submission Through Strategic Alignment and Rapid Cross‑Functional Execution
Case Study: Dossier to Go – Creating an AI Assisted AMNOG HTA Dossier in 3 Months
Case Study: Restructuring Market Access – Driving Alignment and Efficiency in Germany
Case Study: Securing AMNOG Alignment for a Drug Launch in Germany
Case Study: Innovative Outcomes Research in Ophthalmology: Restructuring the Value Story Through Redesigned Cost-Effectiveness Modelling
Case Study: German Dossier Ready in 40 Days for a Renewed Benefit Assessment
Get in touch
Contact us to discover how we can support your journey towards pharmaceutical market access & patient access.
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