AMENDMENTS
Step by step guide to using IRAS for combined review - Health Research Authority
Substantial Amendment Notification Form | PDF | Clinical Trial | Government
3. Notification on the clinical trial of medicinal products for human use. A joint publication of the Federal Institute for Drug
Guidance document for clinical trials sponsors
Step by step guide to using IRAS for combined review - Health Research Authority
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Regulatory and Start-up Guideline for Clinical Trials Germany
Document Title: Amendments to Research Studies Document Number: SOP037
New online submission of amendments and amendments tool launches 2 June - Health Research Authority
Natural Health Product Licence Amendment and Notification Form User Guide - Canada.ca
NOTICE OF SUBSTANTIAL AMENDMENT
Sickness Notification : SweldoMo Automated Payroll & HR Management System Solutions
Detailed guidance on the application format and documentation to be submitted in an application for an Ethics Committee opinion
Guidance for the Submission and Conduct of Clinical Trials (CT) with Medicinal Products
Federal Register :: Amendments to Form ADV
SLaM-IoPPN RD Sponsorship Guidance non-CTIMP amendments - for investigators
Substantial Amendment Notification Form | PDF | Clinical Trial | Government
End of Trial Declaration
AMENDMENTS
Substantial Amendments
Combined Ways of Working Pilot: Post approval submissions
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Federal Register :: Electronic Submission of Applications for Orders Under the Advisers Act and the Investment Company Act, Confidential Treatment Requests for Filings on Form 13F, and Form ADV-NR; Amendments to Form
1302-Preparation of an Application for Allowance
714-Amendments, Applicant's Action
Advance Directive Form Tennessee | pdfFiller
Fillable Online www2 le ac Notification of Amendment (Not Substantial) - University of Leicester Fax Email Print - pdfFiller
