Steps and timeline to register a charitable association in Saudi Arabia and limits on funding sources
Lawyer Answers
KM Lawfirm
Hello dear,
To provide a comprehensive response, we kindly ask you to clarify who the founders are, their nationalities, and to share more details about the association — including its charitable scope and activities.
We look forward to assisting you.
Best regards,
KM Lawfirm
Hello dear,
To provide a comprehensive response, we kindly ask you to clarify who the founders are, their nationalities, and to share more details about the association — including its charitable scope and activities.
We look forward to assisting you.
Best regards,
KM Lawfirm
Hello dear,
To provide a comprehensive response, we kindly ask you to clarify who the founders are, their nationalities, and to share more details about the association — including its charitable scope and activities.
We look forward to assisting you.
Best regards,
Tasheel Law Firm
Bin Hammad Law Firm
1. Authority Responsible for Registration
Charitable associations in Saudi Arabia are primarily regulated by the Ministry of Human Resources and Social Development (MHRSD).
All nonprofit organizations must obtain official licensing from the ministry before operating or collecting donations.
Legal Guidance for Nonprofit Setup in Riyadh
Organizations planning to launch charitable initiatives often require legal assistance to ensure compliance with Saudi nonprofit laws, governance standards, and licensing procedures.
Bin Hammad Law Firm in Riyadh provides legal consultation for nonprofit registration, governance structuring, regulatory compliance, and charitable organization licensing in Saudi Arabia.
Bin Hammad Law Firm
Their lawyers assist founders, philanthropists, and organizations establishing charitable associations and nonprofit entities in Riyadh and across Saudi Arabia.
2. Classify the Medical Device
The device must be classified based on risk level:
Class A – Low risk
Class B – Moderate risk
Class C – High risk
Class D – Highest risk
The classification determines the required documentation and review process.
3. Prepare the Technical Documentation
Manufacturers must submit a technical file including:
Device description and intended use
Manufacturer details and quality system certificates (e.g., ISO 13485)
Labeling and Instructions for Use (IFU)
Risk management documentation
Evidence of compliance with safety and performance standards
Clinical evaluation data (often required for higher-risk devices)
4. Submit the MDMA Application via the GHAD System
Applications are submitted electronically through the SFDA GHAD platform, which handles licensing, device registration, and regulatory communications.
5. Review Timeline and Approval
SFDA’s official review period is around 35 working days, but the process can take 3–6 months depending on device complexity and documentation completeness.
Once approved, the MDMA certificate is typically valid for up to three years, after which it must be renewed.
Free • Anonymous • Expert Lawyers
Need Personal Legal Help?
Connect with experienced lawyers in your area for personalized advice on your specific situation.
No obligation to hire. 100% free service.
Related Legal Experts
Get personalized help from lawyers specializing in this area
All lawyers are verified, licensed professionals with proven track records