In addition, there must be a support system where the software's customers can contact the vendor, ask questions and obtain technical support. The software must have a manual, and the vendor must have policies and procedures in place in order to notify users of issues with the software that have an impact on clinical practice. In order to obtain FDA approval, the software vendor must fulfill several requirements. Once approval has been granted, the item is deemed clinically compliant and can be used in a clinical environment, as long as it continues to meet this standard. The FDA is responsible for approving a wide range of medical items, from drugs and food additives to medical devices. Simply put, a product with 'FDA approval' means that the FDA has certified that the medical benefits of the product outweigh the potential risks of its use. With all that said, are Horos and OsiriX FDA-approved? What Is FDA Approval? Please note that this article does not constitute legal advice, and you should always consult with your attorney or another legal expert if you're uncertain about the legal implications of a decision about your practice.

There are a vast number of regulatory organizations around the world, from Health Canada to the European Union, responsible for approving software for medical use, and the regulations vary from country to country and industry to industry. With that said, no one single answer can apply for every person reading this article. While we will get to the answer, the real question is whether or not Horos or OsiriX meet the standards required for your specific use case. Those who want to use Horos or OsiriX as a medical image viewer are sometimes concerned as to whether the software has been approved by the FDA.

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