is a nonprofit clinical research organization focused on answering the biggest questions around allergies and asthma. We conduct studies for companies exploring the new frontiers of medication, medical devices, or treatments for food allergies, environmental allergies, and asthma.
Seattle Allergy & Asthma Research Institute (SAARI) respects your privacy. We understand that your health information is very sensitive. The law protects the privacy of the health information we create and obtain in providing care and services to you. Your protected information includes your symptoms, test results, diagnoses, treatment plan, and health information from other providers.
SAARI operates http://www.seattleallergy.org. This page informs you of our policies regarding the collection, use and disclosure of Personal Information we receive from users of the Site.
We use your Personal Information only for providing and improving the Site. By using the Site, you agree to the collection and use of information in accordance with this policy.
While using our side, we may ask you to provide us with certain personally identifiable information that can be used to contact or identify you. Personally identifiable information may include, but is not limited to your name, phone number, and email.
Like many site operators, we collect information that your browser sends whenever you visit our site. This Log Data may include information such as your computer’s Internet Protocol (“IP”) address, browser type, browser version, and the pages of our Site that you visit, the time and date of your visit, the time spent on those pages, and other statistics.
For all information relating to patient information will be 21 CFR Part 11 compliant. The prescreen survey health questionnaire also falls under these guidelines. This is the Code of Federal Regulations that establishes the United States Food and Drug Administration regulations on electronic records and electronic signatures. It requires that SAARI implement controls, including audits, system validations, audit trails, electronic signatures, and documentation for software and systems involved in processing the electronic data that FDA predicate rules require them to maintain.