Big news - introducing our new eQMS and improved pricing

We have big news! FormlyAI now has a new eQMS! And better yet, we have new more affordable pricing.

Also, we are excited to announce we have finally released our new electronic Quality Management System (eQMS) that allows you to store and approve your documentation within our Formly software. This makes managing all of that quality and regulatory data easier than ever before. 

We heard your feedback and are providing two pricing plans for users, both that include our new eQMS features. Monthly pricing at the two rates allows you to start earlier and rewards you for finishing earlier. 

In this blog post we are going to break down our new pricing tiers and the features of our new eQMS.

Pricing

More affordable and more rewarding. That was our approach for reformating our pricing.

We now offer two paid subscription plans and an opportunity to try our software for FREE as a trial user! With our monthly pricing, experience the ability to upgrade or downgrade any time.

Give it a shot now.

Premium Subscription

Our premium subscription gives you access to everything you need to get your medical device onto the EU market. Our regulatory roadmap guides you through each step you need to complete in order to have everything ready for certification. Our document assistant creates documents with ease so you are certification ready 10x faster.

Premium+ Subscription

Every great feature of our Premium+ subscription but with the added benefit of our expert regulatory support. We guide you through all of your requirements and check to ensure every document is accurate and ready for regulators. Receive 1:1 weekly calls and a dedicated support channel so that you are never lost along the way.

Formly eQMS

The Formly eQMS is built to make getting your product on the market and keeping it compliant a breeze. With the new FormlyAI eQMS, you can:

• Store and manage all your docs in one place
• Approve documents and track revisions
• Seamlessly make changes to CE marked products
• Stay compliant with ISO 13485

All you need is to invite your team members as approvers to the FormlyAI software and they instantly have access to your device and can approve any documents you invite them to.
It’s one of the easiest ways we have found to create, approve, and manage your documents within an eQMS. Each document contains a signature table, dates, and a revision history so auditors know all your document details instantly. 

As always, your data is stored securely in our EU based cloud servers and each document is available in our document explorer. You can use the document identifiers next to each document to get a quick view of the documents current status, which can be live, draft, or pending approval.

Try it now with our free trial!

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