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Personal Information
Name: Alawia Fathelrahman Tagelsir Mohammed
Nationality: Sudanese
Date of Birth: 1980
Religion: Muslim
Marital Status : Married
Address: Alnahdha – Ibn alhaitham street - Riyadh – Saudi Arabia Mobile No.: +966*********/+966*********
E-mail : ***************@*******.***
Language: Arabic and English
KSA Visa Status: Companion
Qualifications
MBA, Sudan Academy of Sciences, Khartoum, Sudan, Jan. 2017.
M.Sc. in pharmacology; clinical pharmacy specialization, Faculty of Pharmacy, University of Medical Sciences & technology, Khartoum, Sudan, Feb. 2009.
B.Sc. of Pharmacy, Faculty of Pharmacy, University of Khartoum, Sudan, Dec.2003. Work Experience
Regulatory Affairs Consultant Feb. 2014 to Jan. 2017 Duties and Responsibilities:
- Responsible for all regulatory issues regarding registration of companies, pharmaceutical products, cosmetics, medical devices & food supplement for the following companies:
- Life Long Pharmaceutical Co. Ltd.
- Abu sanda Pharmaceutical Co. Ltd
- Muhogany Medical Co. Ltd.
- Sogina For Trade Co. Ltd
- R.S International Co. Ltd
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Work Experience Continue …
Alpha Medical Agencies Co. Ltd Feb. 2009 – Jan. 2014 Business Development Manager & Regulatory Affairs Manager Duties and Responsibilities:
- Responsible for the regulatory issues; registration of companies and products; pharmaceuticals, veterinary, paramedical, cosmetics, food supplements & nutrition.
- Contact with principal suppliers on the regulatory issues (Sanofi-Aventis, Nestle & many other companies from different countries).
- Find opportunities in new markets.
- Classify products according to registration possibility and market potential.
- Supply chain coordinator, making orders & shipping documents follow-up.
- Revision & update the company website.
Federal Pharmacy & Poisons Board (FPPB) Nov. 2007 – Jan. 2009 Rapporteur of the Pharmaceuticals registration committee Duties and Responsibilities:
- Preparation & coordination of the committee meetings.
- Writing the registration committee meeting’s minutes.
- Revision of the committee decisions letters before being received by the companies. MOH - Directorate General of Pharmacy (DGOP) Aug. 2005 – Oct. 2007 Drug Affairs Department – Registration officer
Duties and Responsibilities:
- Revision & evaluation of pharmaceutical products registration files.
- Revision of pharmaceutical products registration certificates.
- Communications, meeting with applicants & solve their problems.
- Collection & revision of data for DGOP website.
- Secretary for the registration committee.
- Revision & update the directorate website.
Alhshaheed Pharmacy – Omdurman Jan 2004 – July 2005 Community pharmacist
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References available on request
Personal & Interpersonal Skills
Good planning
Management skills
Capability of multitasking & good time management
Problem solving
Listening skills
Able to work in team
Ability to learn new
Communication skills
Computer skills
o Microsoft Office (Word, Excel & Power point).
o Internet and email applications.
Training, Seminars & Workshops
o Research methodology – Nov 2006.
o Good Manufacturing Practice (GMP) & Total Quality management (TQM) – Dec 2007.
o Stability studies of pharmaceutical product in 31 Dec. 2009. o How to submit successful registration file in 2010. o Biosimilars: Approval pathways & debated issues in 17 Feb. 2010. o Cosmetic registration in10 June 2010.
o Ethical promotion of pharmaceutical products & medical devise in 21 Oct. 2010. o How to submit successful registration file for local manufacturer from 24-25 Aug. 2013.
o Good Manufacturing Practice (GMP) from 22 -26 December 2013. o Common technical document (CTD) workshop from 9-13 May 2015.