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    Master Pharmaceutical Products Registration In Oman

    Posted By: ELK1nG
    Master Pharmaceutical Products Registration In Oman

    Master Pharmaceutical Products Registration In Oman
    Last updated 1/2022
    MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHz
    Language: 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 virgin 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 virgin 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: Barcoding/Closing

    Lecture 12 Barcoding/Closing

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