Pharmaceutical eCTD & CTD Preparation & Submission, Structure of eCTD, 5 Modules, Practical software Demo, E-Validator
What you will learn
Basic Understanding of CTD & eCTD
Assisting in Compiling & filling and eCTD Application
Identifying EU & US Requirement for eCTD
5 modules of CTD and eCTD
Transiting from Paper based Submission to eCTD Submission
Review eCTD Application
General Demonstration of eCTD Software & eValidator
Regulatory affairs submission documents
Description
The eCTD specification has been developed to facilitate the Global electronic Submission, Review and Lifecycle management of medicinal product dossiers for regulatory applications.
*Complete the course as per your free time as life time access is available.
If you are paying more than 5k INR or $70 for private institute/academy then you are in loss.
Please compare the course description and amount you are paying for such course.
It broadens the scope of the CTD to include information on variations, renewals and amendments, so that it is no longer a static document but is updatable throughout the life of the product. This module outlines the eCTD specification, discusses the approach to regional differences in dossiers, and provides guidance on creation of an eCTD submission.
If you are paying more than 5k INR or $15 for private institute/academy then you are in loss.
Please compare the course description and amount you are paying for such course.
The module provides a training and reference tool that will be of particular value to those new to the use of the format.
This online course details the Electronic Common Technical Document specification, provides guidance on the creation of the submission of an eCTD, and discusses the approach to regional differences in dossiers. This relatively fresh aspect of submissions will undergo significant and rapid changes as specifications are refined and modified further. This class is a superb training tool and reference and can be of assistance to anyone involved with electronic submissions and in navigating these changing requirements.
Once all course requirements have been satisfied, a certificate of completion is immediately available.
Learning Outcome
- Basic Understanding of CTD & eCTD
- Assisting in Compiling & filling and eCTD Application
- Identifying EU & US Requirement for eCTD
- Transiting from Paper based Submission to eCTD Submission
- Review eCTD Application
Course Structure
- Introduction & Overview of CTD
- CTD Fundamentals ( Module 1 – 5)
- eCTD Fundamentals & Details
- Best Practice in Preparing eCTD
- Submission using eCTD Format
- Life Cycle Management for eCTD
- eCTD Software for Compilation & Validation
Who will Benefit ???
- QC/QA Managers & Staff
- Documentation Department
- Regulatory Affairs Department – Responsible for CTD /DMF Preparation & Submission
- Research Chemist, Quality Control Chemist, CRO’s involved in Documentation
- Pharmacy Graduates with knowledge of CTD
- Any science graduates who are seeking job opportunities in Regulatory Affairs
Teaching Methodology
- Participants will be provided with course & study material
- Practical Training will be provided on eCTD.
- Paritcipants can ask their query/questions to the instructor during the course.
Benefits of Getting Certified then job opportunities as
- Regulatory Affairs Associates
- Regulatory Affairs Assistance
- Regulatory Affairs Head/ Director
- Medical Information Associates
- Drug Inspector/Drug Controlle
- Drug Safety Specialist/ Regulatory Food Safety Scientist
- Quality Operations/Quality Control/Quality Assurance
Eligibility
- Life Science Graduates with Experience or Knowledge of Regulatory Affairs
Content