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About us
Who we are
Board
Executive Management
Expressions of Interest
Digital Transformation
Quality Management System
Regulatory Partnerships
Special Projects
Backlog
Vacancies
Tenders
Operational Units
Biologicals
Communication to Industry
Forms
Guidelines
Complementary Meds
Application portal
Communication to Industry
Forms
Guidelines
Templates
Clinical Trials
Communication To Industry
FAQs
Forms
Guidelines
Inspectorate and Regulatory Compliance
Importation – Border Control
Medical Devices
Communication to Industry
Forms
Guidelines
Conformity assessment bodies
Licenced Establishments
Position Statements
Related Documents
Test Kits
Names and Scheduling
Amended Schedules
Consolidated Schedules
Guidelines
Orthodox Medicines
Communication to Industry
Forms
Guidelines
Registered Health Products
Templates
Radiation Control
Communication To Industry
Acts and Regulations
Forms
Guidelines & Codes of Practice
Inspection bodies
News & Updates
Safety Information
Vigilance
Covid-19 Adverse Events Report
Health Product Vigilance
Product Recalls
Rapid Alerts
Recalls Reporting
Report Side Effects
Safety Alerts
Unregistered Products/Section 21
Category A Medicines
Complementary Medicines
Medical Devices
Veterinary Medicines
Veterinary Medicines
Guidelines
Registered Vet Products
Veterinary Portal
Databases & Registers
Medical Devices Licences Issued
OTC Medicines Directory
OTC Toolkit
Pharma Licenced Establishments
Revoked or Suspended Pharma Licences
PI & PIL Repository
Registered Health Products
Registered Vet Products
E-Services
Adverse Drug Reaction Reporting
AEFI Reporting Dashboard
Complementary Medicines Licensing
COVI-VIG Reporting System
Health Product Application Status Checker
Health Products Variations Status Checker
Lot Release Search
OTC Medicines Directory
OTC Toolkit
Product Variations Portal
Med Safety App
Registered Health Products
Section 21 Applications
VET Status Checker
VET Variation Status Checker
E-Library
Corporate & Publications
Annual Reports
Documents For Comments
Fees
Newsletters
Planning Documents
Position Statements
Published Papers
Forms
Guidelines
Guidelines Notice Board
Policies & Regulations
Acts And Regulations
Govt Gazettes And Regulations
Policies
Presentations
Templates
Toolkits
Tutorials
News
News & Updates
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Documents For Comments
Events
NDOH Updates
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Public Information Portal
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THC and CBD Information
Videos
Contact Us
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Clinical Trials Communication To Industry
Document Category
Communication to industry
Guideline
Document Category
Unit
Clinical Evaluations Management
Clinical Trials
Unit
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Document Number
Title
Categories
Date Updated
Version
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File Type
Link
CT03-2023
COVID-19 Clinical Trials – Two-Weekly Progress Reports
Communication to industry
02/01/2024
1
Clinical Evaluations Management
,
Clinical Trials
pdf
Download
Clinical Trial Applications Electronic System
Communication to industry
13/12/2023
1
Clinical Evaluations Management
,
Clinical Trials
pdf
Download
Clinical Trials Committee and Submission Dates for 2024
Communication to industry
,
Guideline
12/10/2023
1
Clinical Evaluations Management
,
Clinical Trials
pdf
Download
Clinical Trials Committee And Submission Dates For 2023
Communication to industry
14/10/2022
1
Clinical Evaluations Management
,
Clinical Trials
pdf
Download
Clinical Trials Committee and Submission dates for 2022
Communication to industry
24/06/2021
1
Clinical Trials
pdf
Download
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