Farah Hammad Email & Phone Number

Amman, Jordan

Amman, Jordan

- Handling under-license projects from dossier audit till registering the product successfully, - Ensure a good alliance between different departments internally and externally with our partners - Support in solving any issue that might be raised during the registration phase and afterward - Ease the communication internally and externally to keep the project within its planned timeline.

Amman, Jordan

- 30++ preparation and submissions of post-approval variation application to health authorities (EU countries (National and DCP/MRP MA’s).- Preparation and submission of renewal applications for existing MA’s (shortened and full renewal).- Contacting over than 40 customers (from EU and non-EU countries) for submitting variations/renewal and following up with them.- Artwork review and approval to be in line with post-approval changes.- Organizing regulatory payments and the recharging of costs to customers.- Update RIMS (Salesforce) to comply with our submissions.

-New Submission files, Deficiency replies, Renewal files, and Post approval changes in MENA (Jordan, Kuwait, Iraq, Bahrain, Egypt, Ethiopia and Azerbaijan)-Visiting Jordan-FDA periodically as the official representative for the company to follow up our submitted new and variation files with the concerned department.-High and direct interaction with international regulatory authorities.-Contacting new suppliers for raw materials and arrange to get approval for them rapidly.

chemistry and regulatory aspects of Carbapol polymers. In the supervision of Hatim Alkhatib, Ph.D. and Suha Al-muhaisen, MSc.

Master'S Degree, Pharmaceutical Sciences

Thesis entitled: “Gliclazide treatment response prediction in type 2 diabetic patients using machine learning techniques”

Bachelor'S Degree, Pharmacy, Excellent (3.77/4.00)