The regulatory efficiency of the medical industry faces huge challenges, and the review of massive documents is time-consuming and labor-intensive. For this reason, an AI supervision assistant called Gandalf came into being. It can automatically review documents submitted by medical device and pharmaceutical companies, significantly improving efficiency and reducing labor costs. Based on Unstructured technology, Gandalf efficiently parses PDF files and achieves rapid review, bringing revolutionary changes to the supervision of the medical industry.
The latest assistant in the medical industry - Gandalf, an AI regulatory assistant that can automatically review documents submitted by medical device and pharmaceutical companies. Gandalf uses Unstructured to parse PDF files. Users only need to upload PDF files, and Gandalf can conduct a comprehensive review within seconds. You can learn more on GitHub: [Link](https://t.co/QxidISWbw6)
Gandalf can check whether materials comply with relevant regulations, laws and regulations, and evaluate whether materials meet the requirements of regulatory agencies (such as FDA or MDR). This innovative technology brings convenience and efficiency to the medical industry and has become the focus of the industry.
The emergence of Gandalf marks the successful application of AI technology in the field of medical supervision and provides a new direction for the future digital transformation of the medical industry. Its efficient and convenient audit function will significantly reduce the work burden of regulatory agencies, improve regulatory efficiency, and ensure the safety and reliability of medical products. We look forward to Gandalf bringing more positive impacts to the medical industry in the future.