Master Pharmaceutical and medical devices products in Sudan
What you'll learn
- Master pharmaceutical Products and medical devices registration in Sudan
- Manage pharmaceutical and medical devices products regulatory pathway in Sudan
- Place your pharmaceutical and medical devices products in Sudan
- Master Sudan market by both pharmaceutical and medical devices products
- Just the PC and welling to stand out of the crowd
Master both pharmaceutical and medical devices products registration in one of the most interesting parts of the African market.
In this course, I will take you on an interesting journey with the Sudan MOH, to master both pharmaceutical and medical devices products registration there, let's practice regulatory affairs, registration, renewal, and variations with all its types, classification, and case-by-case using actual examples from practice. As I always keep my theme in the pharma academy "It comes to you from practice"
In this course, we will cover all topics related to both pharmaceutical and medical device products in Sudan, which 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 comes to you "From Practice", and prepare the submission dossier together, ensure its verification, and interact with the actual system for the submission.
and we will end our journey, by landing at the department of custom clearance, In addition to the pharmacovigilance practice, and the after-sale safety practice.
And finally, congratulations to you for mastering both pharmaceutical and medical devices products registration in the Sudan market, and see you soon in the pharma industry my dear colleagues.
Who this course is for:
- All levels of the pharma industry, starting from the fresh graduates till the highly professionals
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 France
MBA, 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 France
Despite 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.