Master Pharmaceutical Products Registration In Oman

[LeeAndro]

Last updated 1/2022MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHzLanguage: English | Size: 2.78 GB | Duration: 3h 12m

Get a great market share of Sultanate of Oman for pharmaceutical products

What you'll learn
Master pharmaceutical products registration in Sultanate of Oman
Manage pharmaceuticals regulatory pathway in Sultanate of Oman
Get a market share in Sultanate of Oman market
Place your pharmaceutical products in Sultanate of Oman market
Requirements
Just the PC and welling to stand out of the crowd
Description
Master pharmaceutical products registration in one of the most interesting parts of the GCC countries, quite big vi market, full of opportunities, let's grape this huge opportunity and place our pharmaceutical products there in the market of Oman.​

In this course, I will take you on such an interesting journey with the Ministry of the health of Oman, to master our pharmaceutical products registration there, let's practice regulatory affairs, registration, renewal, variations with all its stypes, classification, case by case using actual examples from practice. As I always keep my theme in the pharma academy that "It comes to you from practice"The market of Oman is quite vi compared to other GCC markets, which are actually saturated with most of the kinds of products, such as the leader of the region "KSA" and the gulf region business hup "UAE", which means there is a huge opportunity waiting for us there, to master the market and have quite a big market share with our pharmaceutical products, and do not forget about the tenders, they are basic market players in all GCC countries markets.In this course, we will cover all topics related to pharmaceutical products in Oman, that will empower you to master the market. Then we will go deeper to see the actual forms, and templates as usual I keep the theme of the Pharma Academy that it comes to you "From Practice", and prepare the submission dossier together, and ensure its verification, and interact with the actual system for the submission.we will end our journey, by landing the department of custom clearance, tracking /tracing system, barcoding, 2DMatrix for all the shipments planned for Oman market importation.The system which was first implemented by KSA the leader of the region, and then Oman, UAE, Bahrain followed so far, and the others are coming soon.And finally, congratulations to you for mastering medical device registration in the Oman market, and see you soon in the pharma industry my dear colleagues.See you onboard Let's take-off

Overview

Section 1: Introduction

Lecture 1 Introduction

Section 2: Transition to the eCTD

Lecture 2 Transition to the eCTD

Section 3: Module 1

Lecture 3 Module 1

Section 4: Core eCTD

Lecture 4 Core eCTD

Section 5: Dossier Evaluation

Lecture 5 Dossier Evaluation

Section 6: Validation/Renewal/Variation

Lecture 6 Validation/Renewal/Variation

Section 7: M1 eCTD preparation

Lecture 7 M1 eCTD preparation

Section 8: Country specific elements

Lecture 8 Country specific elements

Section 9: M1 electronic submission

Lecture 9 M1 electronic submission

Section 10: Actual Forms

Lecture 10 Actual Forms

Section 11: eCTD Renewals/Variations

Lecture 11 eCTD Renewals/Variations

Section 12: Barcodilosing

Lecture 12 Barcodilosing

All levels of the pharma industry, starting from the fresh graduates till the highly professionals

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