DocShifter

Can you imagine creating bookmarks in 600 files in just 2 days like this? (Yes, this happens more often than you think.)

Almost everyone in the industry uses ribbons, plugins, desktop tools to format and prepare PDFs for submission-readiness.

There’s obviously nothing wrong with using these. Everyone in regulatory operations, or anyone responsible for formatting documents, is one way or another familiar with these solutions.

Here's the limitation, though: 1 document at a time. Whether the document contains 10 pages or 600 pages, this makes your job even more difficult. They are very ideal when you only want to work on a couple of pages, but not for a full submission.

What is a more efficient way, though?

3-click compliance with DocShifter. (I'll quickly explain.)

1. Select Word or PDF documents you want to include in a US FDA submission
2. Drop these documents in a web browser
3. Get FDA compliant output in a matter of seconds. With the correct bookmarks, hyperlinks, font settings, optimized for fast web view.

I call this 3-click compliance, but you can call it 'winning valuable time back', or 'my work has never been easier'.

Check out more on our latest LinkedIn article: https://eu1.hubs.ly/H07_Dwm0

Who's Paul Ireland for the 3-click compliance session next week?
And no, 3-click is not a buzzword.

Here's an example I will be talking about during the session.

1. Select Word or PDF files to be included in your US FDA submission
2. Upload these to DocShifter via a web browser
3. Get FDA compliant, navigation-rich PDF results back.

OR

1. Choose the Word or PDF files you wish to inspect and correct for non-compliance elements.
2. Upload these to DocShifter via a web browser.
3. Get the fixed Word & PDF files back in no time.

That's where the 3 clicks come from.

Preparing PDFs, reports, or any other content can really be this easy. You do not need to spend hours manipulating PDFs on desktop tools.

Would you like to know or see more? Join Paul Ireland to learn how in our exclusive webinar on January 30.

See you there?



https://eu1.hubs.ly/H07b3Wz0

🚨 Good news for medical device manufacturers!🚨

The U.S. Food and Drug Administration's Center for Devices and Radiological Health (CDRH) has transitioned from paper to electronic export documents for medical devices.

This change streamlines the process for manufacturers, reduces processing times, and minimizes environmental impact.

Read the full article here: https://eu1.hubs.ly/H06Zt1S0