Research Plan (PI) [1]
Title: XXX
Student (name / e-mail): XXX
XXX
Tutor: XXX
Director (name / institution): XXX
XXX
Co-director (name / institution): XXX
XXX
Registration: MM / YYYY
Date: DD / MM / YYYY
1 . Background and current status of the topic
Indicate generally the background and the context in which it is proposed PI, including assumptions and objective / s generals pursued. In this context justify the novelty of the work proposed.
1.1. Previous experience Research Group
Include a brief description of the history of the research group on the proposed topic.
2 . Objectives and approach
Develop specific objectives of the research, describe milestones or partial achievements that arise in the face of achieving the overall objectives outlined in the previous section.
3 . Methodology and work plan
Temporary plan planning activities and tasks indicating their sequentiality and estimated timetable months given that the current legislation promotes the completion of the thesis in a period of three years from the first registration.
3.1. expected impact
Refer to p r esults revistos and the applicability and innovative capacity of the same if it were appropriate. Indicate, providing references to the previous trajectory of the Director and / or Co, the meansproposed (indicating a do mo objective quality) to disseminate the results of the thesis based on the expected results and present the proposed theme, now it must be justified, for example based on recent publications of articles or monographs of other authors comparable to object tr down thesis research objectives.
3.2. Financing plan and mobility
Indicate, based on objective data (average grade student, researcher curriculum history research group, etc.), the possibilities of access to finance for the development of the doctoral thesis.
Include, contributing where appropriate references to previous theses directed by the Director and / or Co – Director, Plan M obility scheduled for doctoral students: rooms that are planned, possible destinations and duration and possible sources of funding for implementation.
4 . Initial Bibliography
The complete reference documentation or material to be taken as a starting point.
signature Doctorando Vº Bº director Vº Bº utor T
ANNEX I: Curriculum vitae of the director of the thesis
Attach a separate document an abbreviated CV of the director, in free form or preferably in the format used by the MINECO, indicating only merit of research and transfer, and of these only referred to the last 6 years.
ANNEX II: Questionnaire on ethics i MPLICATIONS
Indicate whether the proposed research plan contemplates any / s of the following:
A: Research with human beings or use of personal data ……………. ………………… YES NO
B: Use of human biological samples or genetic information ……………………… YES NO
C: Animal Experimentation ………………………………………. ………………………………………….. .. YES NO
D: Use of biological agents of risk to human health, animal or plant YES NO
E: Use of genetically modified organisms (GMOs) ……………………… ……………… YES NO
If the work is done within a broader research project that has the approval of the Ethics Committee of Research (CIS), specify:
- Project heading for:
- Principal Investigator:
- Fcheck approval by the CEI-UAM [2] :
If the research is not part of a project already approved, he is to be sent, together with this Annex, the research plan, which should include the activi ties to be performed, and specify the methodology and material -if applicable- which will ilizar ut.
Apart from the Research Plan with its annexes, will be attached the following documentation:
- Incase A, if the research is prospective, it must provide informed consent document to be used, stating the detailed information you will receive the study participant. If the research is retrospective should establish aconfidentiality about possible data identifying the participants. In any case, it will be detailed if the data or material obtained will be anonymised or coded and how they will It must also state the mode of recruitment of participants. If it comes to clinical experimentation must be attached to the report of the Ethics Committee of the Centre which will be held experimentation, indicating the extent of this authorization (restricted uses the project, or for other related uses).
- Incase B if the investigation is prospective, it must provide informed consent document stating to use the detailed information you receive the study participant. If the research is retrospective authorization of the use of samples, to be treated anonymously, unless the need for treatment of non – anonymous is adequately justified, in which case consent will be required informed and confidentiality document must be submitted.
- Incase C must be attached the Report Manager Animal Welfare (OEBA) Authority and, where appropriate, the Enabled Body.
- In theevent D must be attached to the report of the Committee on Biosafety of the Service or Occupational Health and Safety Center in which will be held experimentation. It also should list the use and describe biological containment measures laboratory where they will perform the work agents.
- In theevent E must be attached to the report of the Committee on Biosafety of the Service or Occupational Health and Safety Center in which will be held experimentation. You must declare the category of risk of GMOs employees and their origin and recipient and donor vectors used employees and agencies.
Data necessary for processing by the CEI:
- Thesis title:
- Doctoral student:
- PhD studentPhone:
- PhD studentemail:
- Doctoral program:
- Director:
- Tutor (if the Director is external):
Signature Doctorando Vº Bº Manager Vº Bº Tutor
Date: (and co – director if any) (if applicable)
1
[1] This document must have an orientation extension of five to ten pages, excluding annexes. The completion of sub – paragraphs 3.1 and 3.2 in those programs where academic committees so established shall not be required.
[2] or, where appropriate, the other CIS Collaborating institution with the PhD Program, which will be specified and attached.
