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What's New in June 2021

Since it's summertime, we are bringing you some light reading
on FDA Quality System Regulation & ISO 13485.

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RELATIONSHIP BETWEEN FDA & ISO 13485

FDA ISO13485

The relationship between the FDA and ISO 13485 goes back a long time.

The ISO standard has been in the list of General Consensus Standards since the dawn of times, but there has never been a full alignment between 21 CFR 820 (QSR) and ISO 13485.

It’s like these couples that have been together forever, but they never did the final commitment. You know, changing the residential address, arranging the wedding, the paperwork, the rings, the dresses, the pressure from the parents, the cost of the reception…

In 2016 our lovely ISO 13485 made a significant step, realigning some if its content with the QSR, but although the FDA has “announced” several times its own step, this has now been delayed for several year (at least 5 times).

New rumours say that the FDA should release a draft version of the new QSR in June 2021.

Is this going to be the one? Well, we are already in the end of June and the FDA’s track records are not encouraging, but we want to believe.

Worst case, ISO 13485 is a modern woman, strong and independent, and will stand proud for as long as it takes. Eventually the FDA will go down on his knee, and there will be confetti, doves and rose petals.

Here at SoftComply, we will shed tears of joy thinking of when we could simplify our eQMS, without making sure that every single small difference is captured in the relevant process…

In the meantime, keep faith and stay tuned!

In case you would like to learn more about the SoftComply eQMS Solution on Confluence, please contact us for a live demo.

Note: the content of this article does not want to discriminate the LGBTQIA community by using the he/she notation, feel free to change it as you prefer. We also do not discriminate about religious vs non-religious weddings, civil partnership, hard-core bachelors / bachelorettes and people who put pineapple on pizza. If you feel offended by this content, you missed the point, by miles.

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There are numerous articles in the SoftComply Knowledge-base including:

▪ How-To benefit from the SoftComply Risk Manager features and customization options,
▪ Frequently Asked Questions on why the Risk Manager works the way it does and how you can change various settings,
▪ Additional Tips & Tricks for adding automation on top of the SoftComply Risk Manager features.
How-To benefit from the SoftComply Risk Manager features and customization options,
Frequently Asked Questions on why the Risk Manager works the way it does and how you can change various settings,
Additional Tips & Tricks for adding automation on top of the SoftComply Risk Manager features.
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In case you cannot join the webinars, feel free to check out the webinar recordings in our YouTube channel about:

▪ Medical Device Regulations & the FDA compliant QMS Solution in Confluence,
▪ Risk Management in Jira with the SoftComply Risk Manager app, and
▪ Establishing Risk Traceability in Jira and Confluence.
Medical Device Regulations & the FDA compliant QMS Solution in Confluence,
Risk Management in Jira with the SoftComply Risk Manager app, and
Establishing Risk Traceability in Jira and Confluence.
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Benefits of the SoftComply Risk Manager PLUS for Jira Server:

▪ Supports Hazard Analysis and FMEA
▪ Supports FMEA with Detectability
▪ Displays risks in Matrices & RPN
▪ Supports FDA approval and CE-marking process
▪ Targeted towards safety critical domain users
Supports Hazard Analysis and FMEA
Supports FMEA with Detectability
Displays risks in Matrices & RPN
Supports FDA approval and CE-marking process
Targeted towards safety critical domain users

For full list of features of SoftComply Risk Manager PLUS, please check out the User Guide. Try it out for free for a month and/or contact us to get a demo & discussion about the features.

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Benefits of the SoftComply eQMS:

▪ Full Quality Management System for medical device co-s
▪ On ISO13485, IEC62304, ISO14971, FDA 21CFR 820
▪ Fully customizable with embedded guidance
▪ Reduces the cost of compliance
▪ Most competitive price
Full Quality Management System for medical device co-s
On ISO13485, IEC62304, ISO14971, FDA 21CFR 820
Fully customizable with embedded guidance
Reduces the cost of compliance
Most competitive price

SoftComply eQMS on Confluence Cloud:

The new MDR states that Quality System documents need to be searchable. You can now implement a compliant Quality System documentation on your Confluence Cloud! Access the free trial version directly from the Atlassian Marketplace and/or contact us to get a demo & discussion about the content of the product.

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Benefits of the SoftComply Risk Manager:

▪ Supports any software system/product risk management
▪ For both Jira Server & Cloud users
▪ Fully customizable for any type of risk project
▪ Automated traceability
▪ Support software system/product risk management
▪ Most competitive price
Supports any software system/product risk management
For both Jira Server & Cloud users
Fully customizable for any type of risk project
Automated traceability
Support software system/product risk management
Most competitive price

For full list of features of SoftComply Risk Manager, please check out the User Guide. Try it out for free for a month and/or contact us to get a demo & discussion about the features.

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