Phizzle

07/10/2025

Curious how AI is transforming cleanroom operations in Pharma Manufacturing?

In this short video, Phizzle Chief Innovation Officer, Mike Patrick, walks through a live demo of the EDGE Puck, our purpose-built device that enables AI at the edge to validate, harmonize, and streamline environmental monitoring in FDA-regulated environments.



https://youtu.be/_RwmuIK3p84?si=JWmoRnHXg0kCo7Su

06/17/2025

The Phizzle EDGE Puck is here, and the real value starts NOW.

If you're in Pharma or any regulated industry, it's time to get hands-on.
See how the EDGE Puck delivers data integrity at the source, where it matters most.

Book a demo today: https://www.phizzle.com/request-a-demo-phizzle-edge-puck

06/05/2025

Introducing the Phizzle EDGE Puck: The only malware-hardened, vendor-neutral platform that formats edge data from any device.

Read the full press release here and reserve your spot for our live technical webinar on June 10th.

Phizzle unveils the EDGE Puck—the first malware-hardened, purpose-built gateway for Pharma. Join our June 10th webinar to see how it formats and normalizes data from any device, enabling automation and compliance at the IoT Edge.

03/12/2025

Manufacturing Ex*****on Systems (MES) are essential for bridging the gap between production and data integrity in BioPharma. But how do they work, and why are they so critical for manufacturing?

We break it all down in the latest Phizzle blog. Check it out!

How is your organization leveraging MES for better compliance and productivity? Drop a comment and let us know!

What is MES?A Manufacturing Ex*****on System (MES) is a highly intelligent computerized system used in manufacturing facilities to monitor, control and manage the entire production process on the manufacturing floor. Its purpose is to ensure efficient ex*****on of manufacturing operations at every s...

03/06/2025

Discover the pros and cons of integrating LIMS into your lab operations! Streamline workflows, boost data accuracy, and enhance efficiency—but is it the right move for your team? Read Phizzle's latest blog to find out.

If you don’t already know, LIMS is a software based solution used to manage and boost efficiency of the workflows for laboratory operations.It includes sample management, data management, workflow management, compliance and traceability, reporting and analytics, inventory management, integration w...

03/04/2025

Yesterday was a great first day for Phizzle at Pittcon! We appreciate LabWare, Inc.’s hospitality at their booth.

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02/20/2025

What is LIMS? Everything You Need to Know

In today’s fast-paced lab environments, data integrity and efficiency are critical. But how does a Laboratory Information Management System (LIMS) fit into the equation?

Our latest blog breaks it all down—what LIMS is, why it matters, and how it can transform lab operations.

Read more here

The basics of LIMS and its application in less than 5 minutes. First, What is LIMS? “LIMS” stands for Laboratory Information Management System.LIMS is a software based solution used to manage and boost efficiency of the workflows for laboratory operations.It includes sample management, data mana...

02/13/2025

Ready to go paperless in 2025? It’s time to take your Air Particle Counters digital and unlock the full potential of data integrity!

Phizzle's latest blog breaks down how to reduce manual processes, improve data management, and transform your workflows for accuracy, compliance, and efficiency in BioPharma manufacturing.

Read more here.

Although many industries have fully embraced paperless practices, the pharmaceutical industry has yet to make this shift in parts of their manufacturing process. But it’s not because they are reluctant to digitize, it's actually quite the opposite.Through our discussions with companies behind some...

02/06/2025

What if your lab techs never had to manually operate air particle counters, retrieve paper printouts, or hand-transfer data into databases again?

The result? 40% productivity boost for one of the world’s largest pharma manufacturers and significant cost savings across the board.

In Phizzle's latest blog, we explore how Digital Air enables remote operation of air particle counters and automates data collection—eliminating manual processes while staying 100% 21 CFR Part 11 compliant and integrating seamlessly with existing LIMS systems.

Read more and discover how you can cut costs and increase productivity

If your lab techs no longer had to physically operate air particle counters to take samples… No longer needed to retrieve paper print outs from these instruments to copy them with a pen and paper…And never had to manually input air particle counter results into a database…What would happen? An...

01/27/2025

Discover how digitization can drive efficiency, reduce failures, and mitigate risks - all while achieving a conservative 1000% ROI. Ready to see how much your company can save?

Read Phizzle's latest blog and calculate your ROI

After over a year of collecting data from the life sciences manufacturing industry and our customers …Including one of the five biggest pharmaceutical companies globally. We’ve created a simple ROI calculator that allows any company currently operating air particle counters… To see how much mo...

01/21/2025

Outdated workflows are holding pharma back from AI’s full potential.

Phizzle’s Digital Air automates data collection, enables remote sampling, and ensures compliance—saving time, cutting costs, and paving the way for AI-driven growth.

Unlock 1000% ROI. Read More.

The buzz around AI and its potential to drive business growth is everywhere.However, the real challenge for many organizations lies in lacking the foundational systems and processes needed to harness its power.This issue is especially pronounced in the pharmaceutical industry, where outdated pen-and...

01/13/2025

Incomplete or inconsistent air quality monitoring logs are a leading cause of audit red flags. Why take the risk?

Phizzle Digital Air’s 21 CFR Part 11 Compliant Solution offers:

*Automated data capture to eliminate manual errors
*Real-time compliance tracking to address issues proactively
*Enhanced data integrity to safeguard against audits

Our customers have cut FDA audit costs by 50% - Read our latest blog to learn how

We all know the critical role compliance and data integrity play in life sciences manufacturing. Regulatory bodies, like the FDA, aren’t just watching…They’re actively looking for gaps in compliance.Auditors are trained to find red flags, and sometimes, they’re just waiting for a reason to d...