Certificate of Release of Shipment of Pharmaceutical Products...

Service completion duration

3 working days

Service fees

Fees for the release of a shipment of pharmaceutic...

Export as

Export as PDF

Export as XLS

Service Rating

Average Rating : From 0 users

About the Service

This service enables customers to apply for a release certificate for a shipment of pharmaceutical products extracted from biological sources, in order to facilitate the issuance of an import permit, ensure the conformity of documents and certificates, and ensure that the product is safe for treatment.

Service Process

1
Login to the MoHAP website or smart app using the UAE PASS
2
The applicant must submits the application online and pay the service fee
3
The certificate will be issued within 3 working days
4
The applicant should courier the original / legalized documents to Drug Department, MOHAP HQ, Dubai

Conditions & Requirements

* Registration Certificate must be submitted if the final product is registered with the Ministry.
* Registration certificate in the country of origin and Purchase orders from the end users must be submitted by the applicant where the product is not registered in the UAE.

Service completion duration

3 working days

Service fees

Fees for the release of a shipment of pharmaceutical products derived from biological sources: AED500

Service channels

MOHAP Website

Service locations

MOHAP website

Support

import.export@mohap.gov.ae

Payment channels

E- Payment

Target audience

Drug Stores, Local pharmaceutical factories, Government Hospitals

Resources

Infographic_Certificate of Release of Shipment of Pharmaceutical Products Derived from Biological Sources

Department name

Drug

Sector name

Health Regulation

Main service

Clearance, Import and Export Permits

Service Code

110-02-025-000

Service Classfication

Transactional

Service Type

Government to Business

Sub Service Type

Variation

Number of Transactions

915

Notes

This service accepts documents authenticated with the UAE PASS Digital Seal.

Required Documents

Required documents for the products derived from Human Blood and Vaccines:
- Original batch release certificate issued by OMCL in country of origin / Legalized copy
- Original Certificate of Final Product Analysis signed, stamped and duly authenticated / Legalized copy
- Invoice
- Report of the production process flow, from beginning to final product (Protocol of manufacturing and Analysis)
- LPO, Declaration and Technical report about consumption from end user
- Copy of pharmacist's and warehouse licenses
- Certificate of Pharmaceutical Product
- WHO prequalification certificate for Vaccines
Required documents for the products of Human Tissue Origin:
- Valid Tissue Bank Certificate of the exporter
- FDA/Authority License for the manufacturer and Product
- Storage and Handling temperature details
- Invoice
- Copy of pharmacist's and warehouse licenses