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Register healthcare products centrally in the GCC by SFDA

Central Registration with GHC
0.0
0.0/5
(0 reviews)
2 students
Created by Dr. Zahra Hassan

9.8

CourseMarks Score®

10.0

Freshness

N/A

Feedback

9.1

Content

Platform: Udemy
Price: $11.99
Video: 4h 8m
Language: English
Next start: On Demand

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Detailed Analysis

CourseMarks Score®

9.8 / 10

CourseMarks Score® helps students to find the best classes. We aggregate 18 factors, including freshness, student feedback and content diversity.

Freshness Score

10.0 / 10
This course was last updated on 3/2021.

Course content can become outdated quite quickly. After analysing 71,530 courses, we found that the highest rated courses are updated every year. If a course has not been updated for more than 2 years, you should carefully evaluate the course before enrolling.

Student Feedback

We analyzed factors such as the rating (0.0/5) and the ratio between the number of reviews and the number of students, which is a great signal of student commitment.

New courses are hard to evaluate because there are no or just a few student ratings, but Student Feedback Score helps you find great courses even with fewer reviews.

Content Score

9.1 / 10
Video Score: 8.2 / 10
The course includes 4h 8m video content. Courses with more videos usually have a higher average rating. We have found that the sweet spot is 16 hours of video, which is long enough to teach a topic comprehensively, but not overwhelming. Courses over 16 hours of video gets the maximum score.
Detail Score: 9.7 / 10

The top online course contains a detailed description of the course, what you will learn and also a detailed description about the instructor.

Extra Content Score: 9.5 / 10

Tests, exercises, articles and other resources help students to better understand and deepen their understanding of the topic.

This course contains:

0 article.
8 resources.
0 exercise.
0 test.

Table of contents

Description

Central registration, the most updated ever pharma industry interesting topic. The topic which has been always on the table for discussion, many time ago till it has been enforced finally in 2021.
The central registration through the Gulf Health Council “GHC” for pharmaceutical products so far, and very soon will be applicable also to the medical devices.
As regulatory affairs professional you must keep up to date with the changing regulations especially in the META region
The central registration option allows you to make only one single submission, one single dossier for your product, that will be approved in all other GCC countries, so going central, means going to the whole GCC region by only one submission.
Still, you have to submit t individually to each country, but t is just admin work, and the dossier has already been revised and proved by the Gulf Health Council, so it takes 2 months instead of 1 year, that sound great? for sure
However, soon you will not have to submit individually any more after central registration submission
Central registration is mandatory for the pharma industry business as it is not allowed to apply for the tenders in the GCC region unless you have central registration, those tenders cannot be missed for any company to achieve the potential ROI.
In this course, we will cover everything related to the topic of the central registration
Staring by Gulf Central Committee For Drug Registration, Human drugs Centralized Registration Process, Module 3 insights, Company (Site/MAH) Centralized Registration, GCC Guidelines for Renewal of Marketing Authorizations, GCC Guidelines for Variation Requirements, GCC Guidelines for Variation Requirements, GCC Guidelines for Presenting the SPC, PIL and Labeling Information, GCC Guidelines for Stability Testing of Active Pharmaceutical Ingredients ( API) and Finished Products ( FPS), GCC Guidelines for the Storage and Transport of Time and Temperature-Sensitive Pharmaceutical Products, and finally the central site audit.
Let us master central registration together.

Requirements

• Just the PC and enough time , block at least 2 hours

You will learn

✓ By the end of this course you will master central registration of pharmaceutical products to the whole Gulf region By only one dossier for one single submission
✓ Central registration of pharmaceutical products to the whole gulf by only one dossier
✓ Central registration of pharmaceutical products through SFDA
✓ Central registration of pharmaceutical products through Saudi Arabia to the whole gulf region
✓ Only one dossier submission per pharmaceutical product to the whole gulf region
✓ Only one dossier submission per pharmaceutical product to be approved in the whole gulf region

This course is for

• Pharma industry regulatory affairs populations, either fresh graduates or professionals looking for career development, or those who would consider to start their own business as freelancers or outsourcing

How much does the Register healthcare products centrally in the GCC by SFDA course cost? Is it worth it?

The course costs $11.99. And currently there is a 87% discount on the original price of the course, which was $94.99. So you save $83 if you enroll the course now.

Does the Register healthcare products centrally in the GCC by SFDA course have a money back guarantee or refund policy?

YES, Register healthcare products centrally in the GCC by SFDA has a 30-day money back guarantee. The 30-day refund policy is designed to allow students to study without risk.

Are there any SCHOLARSHIPS for this course?

Currently we could not find a scholarship for the Register healthcare products centrally in the GCC by SFDA course, but there is a $83 discount from the original price ($94.99). So the current price is just $11.99.

Who is the instructor? Is Dr. Zahra Hassan a SCAM or a TRUSTED instructor?

Dr. Zahra Hassan has created 7 courses that got 3 reviews which are generally positive. Dr. Zahra Hassan has taught 7 students and received a 3.5 average review out of 3 reviews. Depending on the information available, Dr. Zahra Hassan is a TRUSTED instructor.

More info about the instructor, Dr. Zahra Hassan

Pharma industry expert
This is Zahra Hassan, I’m a pharmacist, with almost 10 years of experience in the pharma industry, my experience is extended to cover the regulatory affairs field, which deals with registration and granting health authorities approval for health products, including medicines, medical devices, over the counter products “OTC”, such as food supplements, and cosmetics as well.This is in addition to the quality compliance, control, and assurance for these health products, and also ensuring product safety through pharmacovigilance activities.I have been practicing all these professions for 10 years covering 20 countries, across the regions of the Middle East, Africa, Levant, and Turkey.During my career journey, I gave myself lots of credits by postgraduates studies Msc of pharmacovigilance Bordeaux university FranceMBA, Chiffley buisneiss school , Australia Dual Diploma of regulatory affairs “pharmaceutical and medical devices” RAP society, USA.Certified lead auditor currently enrolled in the Ph.D. program of pharmacovigilance Bordeaux university FranceDespite the fact that postgraduate studies for sure will add to the profile, but the practice is something else, in the begging of my career journey I was chasing professionals asking for private lessons after work to gain practical experience from them, and it was not for free, I used to make this deal with many professionals as I can to get as much diverse experience that I can gain, in addition, I used to follow national and international pharma industry events attending, then participating from my own pocket. This simply happens when you follow your passion.

9.8

CourseMarks Score®

10.0

Freshness

N/A

Feedback

9.1

Content

Platform: Udemy
Price: $11.99
Video: 4h 8m
Language: English
Next start: On Demand

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