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A fee based consultancy service to developers of pharmaceuticals, biopharmaceuticals, medical devices and diagnostics

Our scientific advice services are uniquely positioned to:

  • help you develop evidence that demonstrates the value of your product
  • provide detailed feedback on your clinical, economic development and evidence generation plans
  • help to integrate cost-effectiveness considerations into your evidence generation plans
  • provide support from the highest calibre independent experts within the NHS
  • give you access to the perspective of our patient experts
  • help companies understand health technology assessments, and the perspective of decision makers.
 

Our advice helps you prepare for NICE evaluations and supports discussions with payers and commissioners to enable market access.

Get in touch

Complete the online form to:

  • make an enquiry
  • arrange a site visit or seminar
  • request a speaker
  • sign up to receive updates on our products, services, news and events.

When to use our services

You can request our advice on medicinal products as well as cell and gene therapies, medical devices and diagnostics. We welcome requests from companies developing screening tests and non-therapeutic vaccines. It is important that advice is sought prior to clinical development plans being finalised.  For more detail on timings, look at our frequently asked questions

Medtech

  • Proof of concept, prototype phase

    Get an early insight into building an evidence base to demonstrate the value of your technology and meet the needs of HTA bodies, commissioners and payers with our META  tool©.

  • Evidence generation phase

    Identify any gaps in your evidence generation plans  and receive information on the next steps using our META tool©.

    Optimise your clinical trial/study plans by getting answers to your questions and receiving key insights through our advisory services

  • Adoption phase

    Identify any gaps in the existing evidence base for your technology and receive information on the next steps with the META  tool©. 

Pharmaceuticals

  • Pre-clinical / Phase 1

    Initiate early dialogue with us when your technology does not fit the conventional development paradigm and there is uncertainty around your evidence generation plans.

  • Phase 2 and 3

    Optimise your clinical trial/study plans by getting answers to your questions and receiving key insights through our advisory services.

  • Post phase 3, pre-authorisation

    Optimise any further clinical trial/study plans by getting answers to your questions and receiving key insights through our advisory services.

    Seek expert technical advice on the structure, transparency and overall suitability of your economic model with our PRIMA service.

  • Post-authorisation

    Optimise any further clinical trial/study plans by getting answers to your questions and receiving key insights through our advisory services.

    Seek expert technical advice on the structure, transparency and overall suitability of your economic model with our PRIMA service.