Forms and Guidelines

Clinical Trials

All guidelines, templates and further forms for this programme can be found in the below list.

Guidelines, templates and further forms for this programme were supplemented by the topics of sustainability in funding activities, dealing with risks in international cooperation and the use of generative “artificial intelligence” (AI).

Details on the specific scope of change and the applicable transition periods can be found under the following link.

Please note: As of now, please use the new guidelines and proposal templates of the respective programmes. As of 1 September 2024, proposals following the old model are no longer accepted. The additions regarding the handling of generative AI in the “Guidelines for the Review” apply with immediate effect.

Proposal Submission

Feasibility studies involve a one-stage application process. Proposals must be submitted directly. Proposals for funding feasibility studies can be submitted at any time.

Interventional trials involve a two-stage application process. In the initial stage, draft proposals are to be submitted. Draft proposal may be submitted at any time. Proposals may be submitted only after explicit invitation by the DFG. The invitation will be based on a previously approved draft proposal.

If an interventional trial is proposed on the basis of a feasibility study funded under this programme, the submission of a draft proposal is not required. In this case, a proposal can be submitted directly.

Observational trials also involve a two-stage application process. In the initial stage, draft proposals are to be submitted. Draft proposal may be submitted at any time. Proposals may be submitted only after explicit invitation by the DFG. The invitation will be based on a previously approved draft proposal.

Draft proposals and proposals can be submitted at any time via the DFG’s elan portal.

More information on submitting a proposal can be found in the Guidelines Clinical Trials Programme.

Programme Guidelines

No. Language Title [version] Download
17.01 DE Merkblatt Programm Klinische Studien [09/22] PDF
EN Guidelines Clinical Trials Programme [09/22] PDF

Module Guidelines

No. Language Title [version] Download
52.01 DE Modul Basismodul [09/24] PDF
EN Module Basic Module [09/24] PDF
52.03 DE Modul Vertretung [02/19] PDF
EN Module Replacements [02/19] PDF
52.04 DE Modul Rotationsstellen [09/22] PDF
EN Module Temporary Substitutes for Clinicians [09/22] PDF
52.05 DE Modul Mercator-Fellow [10/11] PDF
EN Module Mercator Fellows [10/11] PDF
52.06 DE Modul Projektspezifische Workshops [09/22] PDF
EN Module Project-Specific Workshops [09/22] PDF
52.07 DE Modul Öffentlichkeitsarbeit [10/11] PDF
EN Module Public Relations [10/11] PDF

Proposal Preparation Instructions

Please use the respective instructions when preparing your proposal. Here, you can find information on which data and information the DFG requires in order to process your proposal.

Draft Proposal

No. Language Title [version] Download
17.03 EN Proposal Preparation Instructions Clinical Trials Programme - Draft Proposals [09/22] PDF

Proposal

No. Language Title [version] Download
17.02 EN Proposal Preparation Instructions Clinical Trials Programme - Proposals [03/24] PDF, RTF

Template for Submitting a Proposal

Please use the relevant template to describe the project. If you cannot use the template, please make sure to use the outline provided.

Draft Proposal

No. Language Title [version] Download
53.13 elan EN Draft Proposal Clinical Trials Programme [09/22] RTF

Proposal

No. Language Title [version] Download
53.14 elan EN Proposal Template – Clinical Trials Programme [03/24] RTF

Supplementary Instructions and Templates

No. Language Title [version] Download
53.200 elan DE Curriculum Vitae [03/23] RTF
EN Curriculum Vitae [03/23] RTF

Interim Reports

Funded interventional trials and observational trials require interim reports to be submitted every six months. Please submit your interim report via email to .

Guidelines for Interim Reports

Please use the guidelines when preparing your interim report. Here, you can find information on which data and information the DFG requires in order to process your interim report.

No. Language Title [version] Download
17.04 EN Preparation Instructions Clinical Trials Programme - Interim Report [06/17] PDF

Template for Submitting an Interim Report

Please use the following template when preparing your interim report. If you cannot use the template, please make sure to use the outline provided.

No. Language Title [version] Download
17.041 EN Interim Report Template - Clinical Trials Programme [06/17] RTF

Other Forms

No. Language Title [version] Download
17.06 DE Verpflichtung auf die Leitlinien zur guten klinischen Praxis (ICH-GCP) [09/21] PDF, RTF