Registration of Medical Devices & Drugs in Overseas Countries

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Export Registration and Approval

We have Experienced and Enthusiastic Professionals that help your Organization to get registered your Facility and Devices as per various Country Regulations in Shortest Possible Time and Cost-effective Way.

African Countries

Ghana, Nigeria, Benin, Burkina Faso, Central African Republic, Congo, Egypt, Ethiopia, Gabon, Liberia, Malawi, Morocco, Rwanda, Sierra Leone, Sudan, Tanzania, Togo, Cameroon, Uganda, Kenya, South Africa.

Gulf / Middle East Countries

Bahrain, Kuwait, Saudi Arabia, Syria, Qatar, Dubai, Oman, Iran

Asian Countries

Bangladesh, Malaysia, Indonesia, Nepal, Sri Lanka, Philippines, Singapore, Thailand, Vietnam, Korea.

Russia / CIS

Russia, Ukraine, Uzbekistan, Belarus, Azerbaijan, Turkmenistan

Latin American

Mexico, Columbia, Argentina

Our professionals help you in:

Developing Your Organization Quality Management System as per 21 CFR 820, ISO 13485
Developing Complete Quality System Documentation
Assisting in Preparation of Technical Document for Your Device
Identifying Tests Required for Your Device
Liaison with the Authorized Distributor/Agent of Your Company in that Country for speeding up the Registration Process
Preparation of Application and Submission
Getting Registration