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EUROPEAN COMMISSION ENTERPRISE DIRECTORATE-GENERAL. Brussels, ENTR/F2/BL  D(2003) CT 1 Revision 2 - PDF Free Download
EUROPEAN COMMISSION ENTERPRISE DIRECTORATE-GENERAL. Brussels, ENTR/F2/BL D(2003) CT 1 Revision 2 - PDF Free Download

Substantial Amendment Notification Form | PDF | Clinical Trial | Government
Substantial Amendment Notification Form | PDF | Clinical Trial | Government

AMENDMENTS
AMENDMENTS

End of Trial Declaration
End of Trial Declaration

Natural Health Product Licence Amendment and Notification Form User Guide -  Canada.ca
Natural Health Product Licence Amendment and Notification Form User Guide - Canada.ca

New online submission of amendments and amendments tool launches 2 June -  Health Research Authority
New online submission of amendments and amendments tool launches 2 June - Health Research Authority

3. Notification on the clinical trial of medicinal products for human use.  A joint publication of the Federal Institute for Drug
3. Notification on the clinical trial of medicinal products for human use. A joint publication of the Federal Institute for Drug

NOTICE OF SUBSTANTIAL AMENDMENT
NOTICE OF SUBSTANTIAL AMENDMENT

Combined Ways of Working Pilot: Post approval submissions
Combined Ways of Working Pilot: Post approval submissions

Substantial Amendment Notification Form | PDF | Clinical Trial | Government
Substantial Amendment Notification Form | PDF | Clinical Trial | Government

Untitled
Untitled

Document Title: Amendments to Research Studies Document Number: SOP037
Document Title: Amendments to Research Studies Document Number: SOP037

Step by step guide to using IRAS for combined review - Health Research  Authority
Step by step guide to using IRAS for combined review - Health Research Authority

Substantial Amendment Notification Form | PDF | Clinical Trial | Government
Substantial Amendment Notification Form | PDF | Clinical Trial | Government

1302-Preparation of an Application for Allowance
1302-Preparation of an Application for Allowance

Federal Register :: Amendments to Form ADV
Federal Register :: Amendments to Form ADV

714-Amendments, Applicant's Action
714-Amendments, Applicant's Action

Guidance for the Submission and Conduct of Clinical Trials (CT) with  Medicinal Products
Guidance for the Submission and Conduct of Clinical Trials (CT) with Medicinal Products

Substantial Amendment Notification Form | PDF | Clinical Trial | Government
Substantial Amendment Notification Form | PDF | Clinical Trial | Government

Substantial Amendment Notification Form | PDF | Clinical Trial | Government
Substantial Amendment Notification Form | PDF | Clinical Trial | Government

Step by step guide to using IRAS for combined review - Health Research  Authority
Step by step guide to using IRAS for combined review - Health Research Authority

Fillable Online www2 le ac Notification of Amendment (Not Substantial) -  University of Leicester Fax Email Print - pdfFiller
Fillable Online www2 le ac Notification of Amendment (Not Substantial) - University of Leicester Fax Email Print - pdfFiller

Natural Health Product Licence Amendment and Notification Form User Guide -  Canada.ca
Natural Health Product Licence Amendment and Notification Form User Guide - Canada.ca

REQUEST FOR AUTHORISATION OF A SUBSTANTIAL AMENDMENT TO A CLINICAL TRIAL -  Ctsu Ox Ac - Fill and Sign Printable Template Online
REQUEST FOR AUTHORISATION OF A SUBSTANTIAL AMENDMENT TO A CLINICAL TRIAL - Ctsu Ox Ac - Fill and Sign Printable Template Online