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Jonah Krakow09/26/233 min read

5 Signs that it is Time to Invest in an eQMS

QualityManagement(QMS)_EasiestSetup_Small-Business_EaseOfSetupThere’s never a bad time to invest in an electronic quality management system (eQMS). As advancements in modern technology allow life sciences companies to continue making staggering breakthroughs, the reality is, organizations that remain tied to manual quality systems will be left behind. 

But here’s the thing, if your company is currently getting organized around its operating budget for next year, it’s an especially good time to allocate resources for a quality management software. 

Here’s why:

Unlike a few years ago, you have options. Now, life sciences companies of all sizes have access to affordable, easy-to-implement quality management tools. The days of expensive, enterprise QMS software platforms reserved only for pharmaceutical giants are over.  (Quality leaders who need help presenting an eQMS business case to their executive team should check out this article.) 

If benefits like process improvement, faster time-to-market, and a lower risk profile for clients/investors aren’t enough to convince you, these five indicators mean it's past time to move from a manual quality system to an eQMS:

1. You’ve lost critical documents 

Losing a document in a sea of binders and file cabinets, or even behind a desk, is a real thing – and it’s awful when it happens. It’s even more of a disaster when you’ve misplaced the actual, final executed copy of a document somewhere in a maze of digital folders. But the worst case scenario? Any of this happening while an auditor or inspector is standing next to you, waiting for answers.

And that’s just the current state. What happens when your company starts to scale? It means more docs and records to manually keep track of, more confusion, and more opportunities for things to get lost. 

2. Your training matrix is too big for spreadsheets

The training matrix is both a blessing and a curse for life science companies. It's an improvement over pencil and paper, and makes it easier to assign training based on job function or role. A spreadsheet-based matrix also helps ensure that trainees are compliant.

However, even a digital training matrix can become an administrative nightmare to maintain and scale. There’s often a breaking point when companies reach more than 20 employees or 50 SOPs. It’s not impossible to handle...it's just harder to keep your training programs organized and easier to make mistakes.  

3. Your workforce includes multiple locations and/or remote workers

The post-pandemic workforce means teams often work with remote employees and contractors from different locations and cities. To stay efficient and compliant in these instances, electronic document signature solutions are a no-brainer compared to scanning, printing, and shipping documents with wet-ink signatures via overnight mail. But watch out – cGMP, cGCP, and other GxP regulated organizations must use quality management tools that are fully validated and 21 CFR Part 11/Annex 11 compliant for e-signatures

4. Your business is being audited frequently

If your business is regularly being audited by your customers and/or the FDA, you know what a drain each one is on resources. Even the best facilities in the world will be judged (sometimes harshly) by an auditor who waits too long for a frantic runner to return from a room full of filing cabinets. It’s not a good look. Put your best foot forward. An eQMS makes it possible to find exactly what the auditor needs in just a few clicks.

Audits don't have to be stressful. Check out these tips for simpler audits before your next regulatory, client, or sponsor audit. 

 

5. Your audits result in Major/Critical findings and/or warning letters/483 from the FDA 

This one is pretty black and white. If you're getting called out for not demonstrating control of your documents, training programs, CAPAs, Change Control, or Audits/Supplier quality programs, your manual system just isn’t working. Please know that an electronic system can help. 

The good news is that most auditors will allow time for eQMS implementation after any observation. So before you race towards the finish line on a thousand other projects, consider shoring up your base with a good electronic system to manage your critical-to-quality activities and boost your risk management.

If you recognize some of these warning signs and want to know how you can overcome them, read about how AavantiBio, a Massachusetts-based biotech, found ZenQMS, an affordable, easy-to-use electronic system that allowed them to move away from paper.

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