About department

A department of the General Directorate of Pharmacy with its main duty of assuring that all of the pharmaceutical products marketed in the Palestine are safe, effective and of high quality. This main duty is achieved by implementing the registration requirements -prepared in the department- that are harmonized with the  international requirements.

The registration process is simply summarized by the comprehensive revision of all the data submitted by the product owners which include the product constituent, manufacturing procedure, quality control procedures, stability studies, clinical information …etc.

Drug Registration Department is responsible for the registration and re-registration of:

 -  Drugs for human and veterinary use

 -  Cosmetic products

 -  Food Supplement

 - Medical Devices

Duties and responsibilities

⌂  Daily follow up of all registration activities.

⌂  Review and approve the pre-approval applications.

⌂  Review and approve the dossier ammendments applications.

⌂  Review and evaluate the re-registration applications.

⌂  Evaluate the drug alerts and cancel the registration of unsafe and harmful medication.

⌂  Publishing registed products list on the pharmaceutuical website (pharmacy.moh.ps).

⌂  Ensure that the registration lists are usually updated.

⌂  Issuing registration certificates, Certificate of Pharmaceutical Products (CPP), Free Sale Certificate (FSC).

⌂  Ensure that the registration process is according to the approved registration guidelines.

⌂  Attending the higher drug technical committee and the registration committee meetings.

⌂  Prepare periodic reports and statistics about the registered products and other activities.

Department email:

registration@moh.ps

Call department:

Tel: 00970 2 2416182 

Fax: 00970 2 2416183