What is the timeline of the STARS project?
The project started on January 1st 2017 and will last for four years. In the first 18 months of the project the tender specifications and contractual arrangements will be elaborated and eventually ‘fine-tuned’ based on the technology maturity and state-of-the-art evidences emerged during the dialogue with industry in the Open Market Consultation.
The tender on the EU website ‘TED’.
Tendering platform Negometrix:
The link to the Negometrix tendering Platform (if Click does not work, please use copy and paste): https://platform.negometrix.com/PublicBuyerProfile/PublishedTenderInformation.aspx?isPublicProfile=false&tenderId=73068&tab=&page=1&searchParam=&sortParam=Id&sortDirection=False
The links to the English help pages to access the Negometrix tendering Platform and Tender documents (if Click does not work, please use copy and paste): https://support.negometrix.com/en/support/home
What is the Open Market Consultation and does the industry have to disclose their technology?
As part of the preparation for an innovation driven procurement action, the market consultation involves the proactive analysis of technology offer and provide a pre-information to the market in order to give a congruous time for the preparation of fit-for-purpose proposals. The STARS market consultation is aimed to these following goals:
• find out whether technologies are commercially available and acquire information about the advantage and disadvantages and the level of coverage of the desired functionalities, in order to confirm the assumption for PCP.
• enable and increase the opportunities for industry to form fit-for-purpose consortia.
• identify market risks potentially able to endanger business goals and supplier performance;
The market consultation sessions are conceived and organized with due regard to the principles of openness, transparency, non-discrimination and equal treatment, in line with European procurement law.
Special attention must be paid to the possibility that such consultations could lead to situations that favour the companies involved, thus distorting competition. During and for the purpose of an early market consultation processes, legal assurances is put in place that suppliers’ intellectual property rights (IPRs), communicated in written form, will be protected. The market consultation will be conducted in the form of open and oral consultations (bilateral, interactive and open workshops). A written contribution (e.g., in the form of a questionnaire aimed to collect market information on innovative and commercialized solution ) could be provided by the participants, to form the basis for more in-depth analysis and assure the confidentiality on the information and solutions described.
If we share our current technology development with the STARS consortium, will this remain confidential?
Yes. We will not share confidential information regarding your technology with any competitors or other outside parties, if provided in written form.
In addition, the STARS team will do everything in their power to be fully transparent in sharing details about the procurement scope and objectives with all interested parties. Therefore, all interested parties will possess the equal amount of knowledge to best understand the innovation challenge and fruitfully participate to the early market engagement activities. A “Procurement Prospectus” will also be published onto the project website: this document will specifically state the objectives that will be pursued through the procurement, the solution desired and the related functional and performance requirements.
We are an innovation driven company, why should we join STARS?
You will have the opportunity to work with highly motivated and experienced professionals from European University Medical Centres and Hospitals, composing a cross-border buyers’ group. We can advise you regarding the research and development and help to innovate.
Your innovative solution will be more likely to be accepted in the medical community than if you would try to create the solution by yourself. Your prototypes will be submitted to test in extensive and bench testing and field tests in human volunteers and patients at much reduced cost.
Are hospitals are willing to pay for stress reduction? What is the business case?
Although we are working on the business case, we know that there is a growing trend for insurances not to pay for costly complications that are seen to be the result of sub-optimal care. If stress reduction can reduce hospital stay and prevent costly or readmissions from home to the hospital (in recently discharged patients), the business case is obvious: one day in hospital is more costly than the total cost of stress reduction.
What about competition? Do we always have at least one competitor within this project?
Yes. In PCP the development of the novelty solution follows a funnel-shaped competitive model. This means that several companies may enter Phase 1 to develop and propose a solution design.
Phase 2 is intended for prototype development. In Phase 3 a pre-market prototype must be developed by industry, which will be tested in our hospitals.
We still need to define the minimum number of competitors in each phase and how to divide the net max budget of 2.7 million euros, which will be paid to the industry. In the published documents all details are explained.