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This Privacy Policy describes how Alzheimer’s Disease Data Initiative, Inc. (ADDI) collects, uses, and shares your personal information when you visit our services or choose to interact with us.

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How to fill out privacy policy

01

Identify the information you collect from users.

02

Explain how you use the collected information.

03

Disclose if you share information with third parties, and for what purposes.

04

Include information on how users can access or change their personal data.

05

Explain the measures you take to protect user data.

06

Provide contact information for privacy-related inquiries.

07

Ensure compliance with relevant laws and regulations.

Who needs privacy policy?

01

Businesses that collect personal data from users.

02

Websites and mobile applications that handle user information.

03

Any organization that processes personal information for marketing or service provision.

04

Companies operating in jurisdictions that require privacy policies by law.

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What is privacy policy?

A privacy policy is a legal document that outlines how an organization collects, uses, stores, and protects the personal information of its users.

Who is required to file privacy policy?

Organizations that collect personal data from users, such as businesses, websites, and apps, are generally required to have a privacy policy in place.

How to fill out privacy policy?

To fill out a privacy policy, organizations should specify the types of data collected, the purpose of data collection, data sharing policies, data protection measures, and user rights regarding their personal information.

What is the purpose of privacy policy?

The purpose of a privacy policy is to inform users about how their personal information is handled and to ensure compliance with data protection laws.

What information must be reported on privacy policy?

A privacy policy must report information such as the types of personal data collected, the purpose of data collection, how data is stored and protected, data sharing practices, and users' rights concerning their data.

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