We help you realise your project
Consultancy services
Do you have a product, practice or technology that you would like to develop or test? On this page you can find out more about the consultancy services we offer.
What we offer
We'll help with a solution - wherever you are in the product journey.
Innovation & Idea
Do you have an idea for a product or solution that you would like to see implemented?
Read more
Safety & CE marking
Are you about to register your new medical device?
Read more
Product Specific Training
Do you want us to run your training or education activities?
Read more
Aftermarket studies
Would you like to see how your product is used in practice?
Read more
Consultancy service
Innovation & Idea
At CAMES, you can draw on experienced engineers, clinicians and scientists - with access to advanced development methods - to help you develop, test and validate your product.
We can help you with every step of the process, from prototype to finished product. We help clarify, develop and qualify a solution for use in the clinical environment. Together with our partners, we work with an evidence-based approach that makes it easy to also collect and analyse data in the clinic. Here you can see how we can help at different stages of the innovation process.
Prototype
CAMES offers a complete package of engineering and production methods - to complete a prototype of your idea.
This process can include CAD design, programming, hardware development, moulding and 3D printing. CAMES collaborates, among others, with the Rigshospitalet Innovation Unit, which offers access to a number of our services.
Contact:
You can also read more - and contact the following units in CAMES:
Usability
Do you want feedback on the usability of your product?
CAMES can set up testing sessions with relevant clinicians / target groups, testing your product in practice - and concluding with oral and written structured feedback and fatback on the design and use of your product.
Contact:
You can also read more under the following units in CAMES:
Test
Do you have a fully developed prototype that you want to test in a practical context?
CAMES can offer structured tests - either on existing or newly developed phantoms - where both the specific and general features of your product can be tested and possibly compared with existing products and methods.
Contact:
You can also read more under the following units in CAMES:
Validation
As a Contract Research Organization (CRO), CAMES offers an extended service in setting up research studies comparing your product with existing products on the market. Either simulation-based or in the clinic.
If there is evidence of improved performance using your product, the results can help you take the product to production or another partner.
Contact:
You can read more - and contact the following entities in CAMES:
Consultancy service
Post-market studies
Would you like to investigate the use of your product?
Clinical studies
Looking for a research partner? As a Contract Research Organization (CRO), CAMES has many years of experience in setting up clinical studies in collaboration between companies, clinicians and hospitals. Particularly when it comes to assessing the impact of education, training and the use of medical devices.
Our research team - consisting of 2 professors, 7 PostDocs and over 30 PhD students - can offer both individual advice as well as independent execution of your studies.
We are specialists in the collection and analysis of clinical data and, as part of Rigshospitalet and the Capital Region, we can also set up methods for the automatic collection and annotation of data with information on both procedures and performance. We also offer anonymisation of data. for other purposes - such as AI-based projects.
Artificial Intelligence
If your product and data are suitable, CAMES offers to set up and validate parameters to assess the quality of use of your product.
These parameters can be used both to assess the impact of education in the form of product-specific training - as well as the quality of the work performed in the clinic.
If these parameters on forward data are also found to be associated with high quality, they can be used to build dynamic models for real-time analysis of collected data. Here, the quality of clinical procedures is looked at as they are being performed - and real time can inform the operator about the quality of the work performed.
You can read more about how we work with artificial intelligence at CAMES AI.
Consultancy service
Safety & CE marking
Are you about to register your new medical device?
CAMES offers a wide range of services to companies facing CE marking of their medical devices, in particular under the European MDR Regulation. For example, we contribute with advice, testing and setting up a validated training programme for future users of your medical devices.
Contact us for individual advice:
Sam Kondo Steffensen, Section Head, CAMES Rigshospitalet
Phone: 31197300 / E-mail: sam.kondo.steffensen@regionh.dk.
Consultancy service
Product-specific training
Building your education
CAMES offers companies to build product-specific training on a scientific basis - including the identification of critical phases in the use of your product.
This includes curriculum design and placing your educational content in a clinical context.
If we deliver your training, we offer you full control over the content of your course in our training platform, where you can set up your course material and training sessions in a well-developed design and learning environment (LMS).
Here you also have the opportunity to take registrations and communicate directly with your students, before, during and after their training.
CAMES can also take care of all administrative matters as required. This could include handling all bookings, participant communication, venues, catering and assistance with everything from air and rail transport - to booking hotels in the local area.
Development of teaching modalities
Special models are needed to test and teach the use of medical equipment.
CAMES collaborates with a number of facilities that offer access to live animal models. However, as our heart beats for the 3R initiative, which is about reducing and making more efficient the use of live animals, we would rather work with you to identify or develop alternative models for your training.
At CAMES, we have extensive experience in producing models for medical education. This allows us to quickly identify the most important parameters for the application of your product - which we can then assemble into a procured or specially produced phantom.
We currently use a number of different models. For example, artificial materials such as silicone and ballistic gel for ultrasound phantoms, as well as biological materials - including specially purified and prepared organ blocks from animals that have already been discarded for other reasons.
Validation of teaching
A validated training programme requires that the content matches the requirements of the users in the clinic. At the same time, it requires a tool, such as a test, that can show with certainty whether users are able to use your product safely - both on models and on real patients.
At CAMES, we have extensive experience of working with validation in a scientific context. Therefore, we are able to offer our efficient and evidence-based methodology as a service to our clients.
We are working with several tools to identify clinicians' needs - including Delphi surveys among professional and educational experts to establish content preferences.
We are also able to build and validate the assessment tools themselves against desired quality parameters, which can then be tested by comparing novices and experts.
Should we build education together?
We match your requirements when it comes to producing simulation-based education, training or courses that have your product as the focal point.
Please contact us if you have any questions - or want to know more.