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Edit Draft using AI in Food

Explore DocHub’s ChatGPT-assisted features to Edit Draft with AI in Food industry

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Aug 6th, 2022

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01. Upload a document from your computer or cloud storage service.

02. Modify your document or let the ai PDF editor summarize, rewrite, or proofread your PDF.

03. Sign your document online in a few clicks.

04. Send, export, fax, download, or print out your document.

How to use DocHub’s functionality to Edit Draft using AI in Food industry

Standard online editors can help professionals in Food industry with simple document management tasks. However, an up-to-date AI-powered solution like DocHub provides more capabilities and helps accomplish your work faster. Select our ChatGPT-powered tool to Edit Draft and other professional paperwork - you’ll get the results you need in minutes!

Explore the quick guideline below to Edit Draft with AI in Food industry:

Create an account in DocHub and log in after its verification.
Add the Draft to the editor using one of the available upload methods.
Launch the ChatGPT assistant and select the tool that lets you Edit your form.
Examine the updates suggested by Artificial Intelligence.
Make edits where necessary, and verify at least once more before submitting.
Add your signature and request it from others if your form needs approval.
Click on Menu to download, export, or share your professional paperwork.

Whatever your document management needs, you can trust our progressive solution and accomplish your tasks in a snap. Try it today!

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Got questions?

Below are some common questions from our customers that may provide you with the answer you're looking for. If you can't find an answer to your question, please don't hesitate to reach out to us.

Can an app be considered a medical device?

The most obvious way to label an app as a medical device is using its intended use. Based on the FDAs guidance document, an application is deemed a medical device if it is utilized in the detection, cure, mitigation, treatment, or prevention of diseases.

What is considered a medical device?

A medical device can be any instrument, apparatus, implement, machine, appliance, implant, reagent for in vitro use, software, material or other similar or related article, intended by the manufacturer to be used, alone or in combination for a medical purpose.

Is AI considered a medical device?

Like other software, AI-based software is classified as a medical device if it provides an effect in connection with, for example, diagnosis, prevention, monitoring, prediction, prognosis, treatment or alleviation of diseases for an individual.

What guidance does the FDA draft to ease path to updates for AI enabled devices?

In its guidance, the FDA said AI- or machine learning-enabled devices can have a docHub positive impact on healthcare. Its goal is to create a least burdensome approach to support iterative improvement through modifications to an AI/ML-enabled device, while continuing to provide a reasonable assurance of device

What is FDA PCCP?

Contents. The Food and Drug Administration (FDA), the US regulating authority in the sphere of healthcare products, has published a draft guidance document dedicated to the content of a Predetermined Change Control Plan (PCCP) for artificial intelligence/machine learning (AI/ML) based medical devices.

Is an algorithm a medical device?

In the US, the FDA has regulatory authority over medical devices, including medical device software. Whether computerized clinical algorithms qualify as FDA-regulated medical devices has been an open question. In 2019, the FDA preliminarily concluded that many computerized clinical algorithms would not qualify.

What is an AI medical device?

For example, the use of AI in telehealth has allowed for the creation of AI chatbots, which can review a patients symptoms and suggest next steps, such as an in-person follow-up where necessary. The FDA granted accelerated approvals of medical devices with AI in 2022, which is expected to continue through 2023.

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