TOPIC : Pilot Lines for 3D printed and/or injection moulded polymeric or ceramic microfluidic MEMS
|Publication date:||14 October 2015|
|Types of action:||IA Innovation action|
|DeadlineModel: Opening date:||two-stage 11 May 2016||Deadline: 2nd stage Deadline:||
27 October 2016 17:00:00
04 May 2017 17:00:00
|Time Zone : (Brussels time)|
Topic DescriptionSpecific Challenge:
Microfluidics devices were initially based on non-polymeric materials like silicon or glass, manufactured in facilities developed for the semiconductor industry. New fabrication techniques that are completely based on polymer/plastic materials can lead to reducing fabrication costs and optimise time, including rapid prototyping methods for a new range of products.
A new generation of 3D micro and nano structured and/or injection moulded polymeric or ceramic microfluidic MEMS products are targeted. Applications may include MEMS for nozzles or filters, sensor applications, lab-on-chip systems, printed biochemical materials, soft substrates etc., and open for new applications, including disposables where production cost need to be kept to a minimum. The adoption of environment friendly material solutions may also be explored (e.g. biodegradable materials, materials from renewable resources, reusable/recyclable materials).
While typical features for the mentioned applications may be larger than leading edge semiconductor processes, the required feature sizes are nonetheless significantly smaller than what is available with current standard printing and injection moulding techniques i.e. micro- and nano-fabrication capabilities are required.Scope:
The proposed pilot lines should address the development, upscaling and demonstration in relevant industrial environments.
They should use existing pilot lines as a starting point for development, incorporating new materials and methods and/or instrumentation with real time characterization for measurement, analysis and monitoring at the nanoscale to characterise relevant materials, process properties and product features.
The aim is to increase the level of robustness and repeatability of such industrial processes; to optimise and evaluate the increased performance of production lines in terms of productivity and cost-effectiveness; and finally to assess the functionality and performance of the new materials/products.
Proposals should address the complete research-development-innovation cycle and obstacles remaining for industrial application, and involve a number of relevant materials producers and users, also considering the needs of SMEs.
Non-technological aspects key for the marketing of such products (e.g. standardization, regulatory issues, user acceptance, HSE aspects, LCA) need to be considered.
Applications may fall within areas such as:
- 3D micro and nano printed and/or injection moulded biological applications (including instrument on a chip, bio-medical/bio-physical sensors, Lab-on-chip, organ-on-a-chip, bio-compatible or toxic scaffolds, active influence of cell growth & differentiation).
- 3D micro and nano printed and/or injection moulded polymeric or ceramic microfluidic MEMS for nozzles or filters, sensor applications, and multi-use chip (including also injection molded nanostructures in polymers).
- In-line process control technologies as well as characterization methods needs to be included in order to meet recognised quality, environmental and safety standards and legislations.
The increased performances of the production lines in terms of productivity and cost-effectiveness should be demonstrated together with the relative improved functionality and performance of the resulting products.
SME needs should be catered for, e.g. through a coordinated network of pilot line, test and validation services, in order to prepare for management decisions to progress to the next step of new technology deployment, i.e. installation of industrial pilot lines and enter the commercialization stage.
Activities are expected to focus on Technology Readiness Levels 4 to 6, and target Technology Readiness Level 7. This topic addresses cross-KET activities.
The Commission considers that proposals requesting a contribution from the EU between EUR 5 and 8 million would allow this specific challenge to be addressed appropriately. Nonetheless, this does not preclude submission and selection of proposals requesting other amounts.Expected Impact:
The action should allow for a new generation of MEMS products.
The scaled up production lines for 3D micro and nano printing and/or injection moulding in combination with the use of polymers and new micro- and nano-fabrication capabilities is expected to increase cost-effectiveness and robustness of the process and resulting products.
Direct benefit to the involved industries should be demonstrated in the form of reduced costs and full consideration of environmental and safety legislation.
Enhanced manufacturing capacities in Europe and/or enhanced market opportunities for European enterprises. These impacts should be addressed in particular in the outline of the business case and exploitation strategy to be submitted with the proposal. The expected content of this outline is further detailed in the LEIT introduction, section 6.
Impact should be presented at three levels:
- Impact on the consortium materials producers and users, and other involved industries, demonstrated in the form of reduced costs and full consideration of environmental and safety legislation;
- Other existing or new materials manufacturers, describing the expected impact from further integration of the nano-enabled multifunctional materials into practical large-scale applications with producers outside the consortium;
- Global impact in form of direct or derived benefits from competitive advantage of the new materials in products.
The impact will also be improved by a contribution to training and knowledge dissemination for building an educated workforce.
Overall the action is expected to help driving the demand in Europe as well as support the penetration of new markets worldwide, also considering the contributions to an improved quality of life from the resulting products (e.g. lab-on-chip, filters and sensors for medical or other applications), ultimately contributing to a significant growth of quality jobs.
This should include clear benefits to manufacturers, including SMEs, and new entrants into the market should be expected.Cross-cutting Priorities:
Topic conditions and documents
Please read carefully all provisions below before the preparation of your application.
- LIST OF COUNTRIES and APPLICABLE RULES FOR FUNDING
described in part A of the General Annexes of the General Work Programme.
Note also that a number of non-EU/non-Associated Countries that are not automatically eligible for funding have made specific provisions for making funding available for their participants in Horizon 2020 projects (follow the links to Australia, Brazil, Canada, China, Hong Kong &Macau, India, Japan, Republic of Korea, Mexico, Russia, Taiwan).
- ELIGIBILITY and ADMISSIBILITY CONDITIONS
described in part B and C of the General Annexes of the General Work Programme.
Proposal page limits and layout: Please refer to Part B of the standard proposal template.
3.1 Evaluation criteria and procedure, scoring and threshold:
The criteria, scoring and threshold are described in General Annex H of the work programme.
The following exceptions apply:
For single-stage and second-stage evaluations, the threshold for the criteria Excellence and Impact will be 4. The overall threshold, applying to the sum of the three individual scores, will be 12.
The procedure for setting a priority order for proposals with the same score is given in General Annex H of the work programme. The following exceptions apply:
Under 3 (a)
Proposals are first ranked in separate lists according to the topics against which they were submitted (‘topic ranked lists’). When comparing ex aequo proposals from different topics, proposals having a higher position in their respective 'topic ranked list' will be considered to have a higher priority in the overall ranked list.
Under 3 (b)
For all topics and types of action, the prioritisation will be done first on the basis of the score for Impact, and then on that for Excellence.
3.2 Submission and evaluation process: Guide to the submission and evaluation process
- INDICATIVE TIMETABLE for EVALUATION and GRANT AGREEMENT
Information on the outcome of two-stage evaluation:
For stage 1: maximum 3 months from the deadline for submission.
For stage 2: maximum 5 months from the deadline for submission.
Signature of grant agreements: maximum 8 months from the deadline for submission.
- PROVISIONS, PROPOSAL TEMPLATES and EVALUATION FORMS
for the type of action under this topic
Specific provisions and funding rates
Standard proposal template
Standard evaluation form
H2020 General MGA -Multi-Beneficiary
Annotated Grant Agreement
- ADDITIONAL PROVISIONS
Horizon 2020 budget flexibility
Technology readiness levels (TRL) – where a topic description refers to TRL, these definitions apply.
Financial support to Third Parties – where a topic description foresees financial support to Third Parties, these provisions apply.
- OPEN ACCESS
Open access must be granted to all scientific publications resulting from Horizon 2020 actions.
Where relevant, proposals should also provide information on how the participants will manage the research data generated and/or collected during the project, such as details on what types of data the project will generate, whether and how this data will be exploited or made accessible for verification and re-use, and how it will be curated and preserved.
Open access to research data
The Open Research Data Pilot has been extended to cover all Horizon 2020 topics for which the submission is opened on 26 July 2016 or later. Projects funded under this topic will therefore by default provide open access to the research data they generate, except if they decide to opt-out under the conditions described in annex L of the Work Programme. Projects can opt-out at any stage, that is both before and after the grant signature.
Note that the evaluation phase proposals will not be evaluated more favourably because they plan to open or share their data, and will not be penalised for opting out.
Open research data sharing applies to the data needed to validate the results presented in scientific publications. Additionally, projects can choose to make other data available open access and need to describe their approach in a Data Management Plan.
- Projects need to create a Data Management Plan (DMP), except if they opt-out of making their research data open access. A first version of the DMP must be provided as an early deliverable within six months of the project and should be updated during the project as appropriate. The Commission already provides guidance documents, including a template for DMPs.
- Eligibility of costs: costs related to data management and data sharing are eligible for reimbursement during the project duration.
The legal requirements for projects participating in this pilot are in the article 29.3 of the Model Grant Agreement.
- ADDITONAL DOCUMENTS
Legal basis: Horizon 2020 - Regulation of Establishment
Legal basis: Horizon 2020 Rules for Participation
Legal basis: Horizon 2020 Specific Programme
H2020 Work Programme 2016-17: Introduction
H2020 Work Programme 2016-17: Introduction to Leadership in enabling and industrial technologies (LEITs)
H2020 Work Programme 2016-17: Nanotechnologies, advanced materials, advanced manufacturing and processing, biotechnology
H2020 Work Programme 2016-17: Cross-cutting activities (Focus Areas)
H2020 Work Programme 2016-17: Dissemination, Exploitation and Evaluation
H2020 Work Programme 2016-17: General Annexes
No submission system is open for this topic.
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