The workshop will be for 2 hours and will be held on the Zoom App.

Make sure you come 10 mins before the scheduled time and have a simple notebook and pen to write the important points you find during the workshop. Attending the workshop on PC and with good internet connectivity is advisable for a better learning experience.

No recordings are provided to ensure every registrant attends the workshop live and gets the best out of the workshop.

Please email us at connect@pharmagrowthhub.com (connect@pharmagrowthhub.com)& our support team will get back to you as soon as possible.

Pharma Growth Hub is an online coaching and training platform specifically designed for pharmaceutical professionals. It offers a wide range of courses and resources to enhance your knowledge and skills in the pharmaceutical industry. It helps in career development.

Pharma Growth Hub is designed for pharmaceutical professionals at all levels, including students, entry-level employees, mid-level managers, and senior executives. Whether you're just starting your career or looking to advance, we have resources for you.

Our platform offers a variety of courses covering topics such as research & development, quality control, quality assurance, and more. We also provide leadership and soft skills training for career development.

Once you create an account and subscribe, you can access our courses 24/7 from anywhere with an internet connection. The platform is mobile-friendly for learning on the go.

Yes, we encourage interaction. You can communicate with instructors, ask questions, and participate in discussion forums to engage with other learners.

The pricing varies depending on the course and the level of access you choose. You can find detailed pricing information on the course pages.

Yes, we have corporate and group pricing packages for organizations looking to provide training to their teams. Please contact our support team for more information.

We offer a satisfaction guarantee. If you're not happy with a course, you can request a refund within the specified refund period. Refer to our refund policy for details.

Yes, once you complete a course, you'll retain access to the course materials, allowing you to revisit the content and resources for reference until the duration mentioned while purchasing.

To get started, simply sign up for an account, browse our course catalog, and choose the courses that suit your needs. You can start learning right away!

You'll need an internet connection, a device (computer, tablet, or smartphone), and a modern web browser to access our platform. Detailed technical requirements are provided in our support section.

Yes, upon successfully completing a course, you will receive a certificate of completion, which you can add to your professional portfolio.

You can reach our customer support team through our contact page, and we'll be happy to assist you with any inquiries or issues.

We periodically host webinars, networking events, and industry-related discussions to facilitate connections and knowledge sharing among our members.

Yes, we offer a mobile-friendly website for learning on the go.

After enrollment, participants receive onboarding details, program expectations, and access instructions for attending live sessions and completing assignments.

Learning is delivered through live online sessions that explain concepts clearly and connect them to real submission workflows. Sessions build progressively — from CTD fundamentals to authoring, AI tools, and eCTD workflow.

A dedicated weekly doubt-clearing session ensures participants can resolve questions, reinforce understanding, and stay aligned with program expectations.

Module-wise assignments focus on practical application — so learners develop clarity on structure, placement logic, and authoring expectations rather than just theory.

Structured guidance and industry-ready templates support CTD authoring across Modules 1–5. Participants learn what each module typically contains and how documents are organized and prepared for submission.

Participants explore how AI is used in CTD authoring and eCTD workflows — including drafting support, gap checking, and consistency review — and understand where AI fits within regulated submission environments.

Demonstration and guided exposure to the eCTD submission process: project setup, sequence creation, submission flow, and lifecycle change concepts.

Introduction to validation expectations and common technical issues: validator rules, typical failures, and understanding full validation checks.

Participants complete the program assessment. Certification is awarded on successful completion and meeting the required performance criteria.

SMART eCTD is a structured, hands-on learning platform designed to build practical competence in CTD authoring, eCTD submission workflow, AI-assisted regulatory documentation, and validation readiness for Regulatory Affairs roles.

This program is suitable for freshers, early-career professionals, and working professionals from QA, QC, Manufacturing, R&D, and Regulatory Affairs who want practical exposure to CTD/eCTD submission practices and AI-driven regulatory workflows.

The program duration is 3 months.

The program is delivered through live online sessions and supported with guided assignments. Session recordings may be made available to enrolled participants for revision purposes — confirm availability at the time of enrollment.

Live sessions are conducted on Saturday and Sunday (7:00 pm to 9:00 pm IST) and Thursday (8:00 pm to 9:00 pm IST).

Yes. Participants receive structured guidance and industry-ready templates to support CTD authoring exposure across Modules 1 to 5.

Yes. The program includes an eCTD submission demonstration and workflow exposure, including project setup, sequence creation, and lifecycle change concepts.

Yes. The program includes a dedicated module on AI automation in CTD/eCTD workflows — covering how AI tools are used for CTD drafting, content review, gap analysis, and submission process efficiency.

Yes. Participants receive exposure to XML validation expectations, including validator rules, typical validation failures, and understanding of full validation checks.

Yes. Participants receive guidance to create an eCTD submission project by selecting a specific drug product and understanding the workflow required for submission readiness.

Participants receive structured learning resources, assignment guidance, and industry-ready templates for CTD module authoring, along with eCTD workflow, AI tools, and validation support materials.

Yes. Certification is provided upon successful completion of the program and meeting the program assessment requirements.

You can contact us at connect@pharmagrowthhub.com (mailto:connect@pharmagrowthhub.com)or WhatsApp +91 9766383968.