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Riyadh, Riyadh Province, Saudi Arabia
November 12, 2017

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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


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


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


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.

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