CURIS BioDecontamination System

08/21/2025

CURIS Academy | Tip Series on MAL Spaces

𝗧𝗶𝗽 #3
𝘙𝘦𝘥𝘦𝘧𝘪𝘯𝘦 “𝘊𝘭𝘦𝘢𝘯” 𝘢𝘵 𝘵𝘩𝘦 𝘵𝘩𝘳𝘦𝘴𝘩𝘰𝘭𝘥

Moving materials into sensitive areas is a nonstop job, and with that comes a high risk for contamination. Automating this process not only streamlines operations but also helps safeguard staff by reducing human error and limiting exposure to harsh disinfectants.

✔️ CURIS – for validated >6-log results, no harsh chemical, no material degradation

Find information on CURIS MAL Chambers:
https://curissystem.com/products/decon-chambers

𝘞𝘩𝘦𝘵𝘩𝘦𝘳 𝘺𝘰𝘶'𝘳𝘦 𝘰𝘷𝘦𝘳𝘴𝘦𝘦𝘪𝘯𝘨 𝘱𝘩𝘢𝘳𝘮𝘢 𝘱𝘳𝘰𝘥𝘶𝘤𝘵𝘪𝘰𝘯, 𝘮𝘢𝘯𝘢𝘨𝘪𝘯𝘨 𝘷𝘪𝘷𝘢𝘳𝘪𝘶𝘮 𝘸𝘰𝘳𝘬𝘧𝘭𝘰𝘸𝘴, 𝘰𝘳 𝘰𝘱𝘦𝘳𝘢𝘵𝘪𝘯𝘨 𝘩𝘪𝘨𝘩-𝘤𝘰𝘯𝘵𝘢𝘪𝘯𝘮𝘦𝘯𝘵 𝘳𝘦𝘴𝘦𝘢𝘳𝘤𝘩 𝘭𝘢𝘣𝘴, 𝘊𝘜𝘙𝘐𝘚 𝘴𝘶𝘱𝘱𝘰𝘳𝘵𝘴 𝘦𝘷𝘦𝘳𝘺 𝘴𝘵𝘦𝘱 𝘰𝘧 𝘺𝘰𝘶𝘳 𝘣𝘪𝘰𝘥𝘦𝘤𝘰𝘯𝘵𝘢𝘮𝘪𝘯𝘢𝘵𝘪𝘰𝘯.

𝘊𝘜𝘙𝘐𝘚 𝘚𝘺𝘴𝘵𝘦𝘮: 𝘊𝘩𝘢𝘯𝘨𝘪𝘯𝘨 𝘩𝘰𝘸 𝘺𝘰𝘶 𝘷𝘪𝘦𝘸 𝘤𝘰𝘯𝘵𝘢𝘮𝘪𝘯𝘢𝘵𝘪𝘰𝘯 𝘤𝘰𝘯𝘵𝘳𝘰𝘭

08/18/2025

CURIS Academy | Tip Series on MAL Spaces

𝗧𝗶𝗽 #𝟮
𝘛𝘳𝘢𝘪𝘯𝘪𝘯𝘨 𝘪𝘴𝘯'𝘵 𝘦𝘯𝘰𝘶𝘨𝘩: 𝘘𝘶𝘢𝘭𝘪𝘧𝘪𝘤𝘢𝘵𝘪𝘰𝘯 𝘮𝘢𝘬𝘦𝘴 𝘵𝘩𝘦 𝘥𝘪𝘧𝘧𝘦𝘳𝘦𝘯𝘤𝘦

Think knowing the protocol is enough? Think again.

244 Citations were issued between 2018–2022 under CFR 211.25 (a) for 𝙞𝙣𝙖𝙙𝙚𝙦𝙪𝙖𝙩𝙚 𝙥𝙚𝙧𝙨𝙤𝙣𝙣𝙚𝙡 𝙘𝙤𝙢𝙥𝙚𝙩𝙚𝙣𝙘𝙮: It’s the #7 most-cited violation in drug manufacturing inspections, but its implications extend well beyond pharmaceuticals... to any environment handling sensitive biological processes.

Read our article on FDA warnings here:
https://curissystem.com/resources/blog/avoiding-fda-warning-letters-why-high-level-biodecontamination-is-essential-in-pharma-manufacturing

✅ 𝘞𝘩𝘦𝘵𝘩𝘦𝘳 𝘺𝘰𝘶'𝘳𝘦 𝘰𝘷𝘦𝘳𝘴𝘦𝘦𝘪𝘯𝘨 𝘱𝘩𝘢𝘳𝘮𝘢 𝘱𝘳𝘰𝘥𝘶𝘤𝘵𝘪𝘰𝘯, 𝘮𝘢𝘯𝘢𝘨𝘪𝘯𝘨 𝘷𝘪𝘷𝘢𝘳𝘪𝘶𝘮 𝘸𝘰𝘳𝘬𝘧𝘭𝘰𝘸𝘴, 𝘰𝘳 𝘰𝘱𝘦𝘳𝘢𝘵𝘪𝘯𝘨 𝘩𝘪𝘨𝘩-𝘤𝘰𝘯𝘵𝘢𝘪𝘯𝘮𝘦𝘯𝘵 𝘳𝘦𝘴𝘦𝘢𝘳𝘤𝘩 𝘭𝘢𝘣𝘴, 𝘊𝘜𝘙𝘐𝘚 𝘴𝘶𝘱𝘱𝘰𝘳𝘵𝘴 𝘦𝘷𝘦𝘳𝘺 𝘴𝘵𝘦𝘱... 𝘧𝘳𝘰𝘮 𝘰𝘯𝘣𝘰𝘢𝘳𝘥𝘪𝘯𝘨 𝘵𝘰 𝘲𝘶𝘢𝘭𝘪𝘧𝘪𝘤𝘢𝘵𝘪𝘰𝘯—𝘸𝘪𝘵𝘩 𝘦𝘹𝘱𝘦𝘳𝘵 𝘨𝘶𝘪𝘥𝘢𝘯𝘤𝘦 𝘣𝘶𝘪𝘭𝘵 𝘪𝘯.

CURIS System: Changing how you view contamination control

08/14/2025

𝗠𝗬𝗧𝗛 𝗩𝗦 𝗙𝗔𝗖𝗧

💭 𝗜𝘀 𝗺𝗼𝗿𝗲 𝗵𝘆𝗱𝗿𝗼𝗴𝗲𝗻 𝗽𝗲𝗿𝗼𝘅𝗶𝗱𝗲 𝗮𝗹𝘄𝗮𝘆𝘀 𝗯𝗲𝘁𝘁𝗲𝗿?

It’s one of the most persistent assumptions in biodecontamination - and one that continues to influence system design and facility protocols.

𝗕𝘂𝘁 𝘄𝗵𝗮𝘁 𝗶𝗳 𝘁𝗵𝗮𝘁 𝗹𝗼𝗻𝗴-𝗵𝗲𝗹𝗱 𝗯𝗲𝗹𝗶𝗲𝗳 𝗶𝘀𝗻’𝘁 𝘀𝘂𝗽𝗽𝗼𝗿𝘁𝗲𝗱 𝗯𝘆 𝘁𝗵𝗲 𝗱𝗮𝘁𝗮?

𝘖𝘶𝘳 𝘭𝘢𝘵𝘦𝘴𝘵 𝘣𝘭𝘰𝘨 𝘤𝘩𝘢𝘭𝘭𝘦𝘯𝘨𝘦𝘴 𝘵𝘩𝘪𝘴 𝘭𝘦𝘨𝘢𝘤𝘺 𝘵𝘩𝘪𝘯𝘬𝘪𝘯𝘨 𝘢𝘯𝘥 𝘪𝘯𝘵𝘳𝘰𝘥𝘶𝘤𝘦𝘴 𝘢 𝘴𝘮𝘢𝘳𝘵𝘦𝘳 𝘢𝘱𝘱𝘳𝘰𝘢𝘤𝘩 𝘵𝘰 𝘩𝘪𝘨𝘩-𝘭𝘦𝘷𝘦𝘭 𝘥𝘪𝘴𝘪𝘯𝘧𝘦𝘤𝘵𝘪𝘰𝘯—𝘰𝘯𝘦 𝘵𝘩𝘢𝘵’𝘴 𝘢𝘭𝘳𝘦𝘢𝘥𝘺 𝘮𝘢𝘬𝘪𝘯𝘨 𝘢 𝘮𝘦𝘢𝘴𝘶𝘳𝘢𝘣𝘭𝘦 𝘥𝘪𝘧𝘧𝘦𝘳𝘦𝘯𝘤𝘦 𝘪𝘯 𝘤𝘭𝘦𝘢𝘯𝘳𝘰𝘰𝘮𝘴, 𝘪𝘴𝘰𝘭𝘢𝘵𝘰𝘳𝘴, 𝘢𝘯𝘥 𝘱𝘳𝘰𝘥𝘶𝘤𝘵𝘪𝘰𝘯 𝘴𝘱𝘢𝘤𝘦𝘴.

𝗦𝗲𝗲 𝘄𝗵𝘆 𝗺𝗮𝗻𝘆 𝘁𝗲𝗮𝗺𝘀 𝗮𝗿𝗲 𝗿𝗲𝘁𝗵𝗶𝗻𝗸𝗶𝗻𝗴 𝘁𝗵𝗲𝗶𝗿 𝗮𝗽𝗽𝗿𝗼𝗮𝗰𝗵 - 𝗮𝗻𝗱 𝘄𝗵𝗮𝘁 𝘁𝗵𝗮𝘁 𝗰𝗼𝘂𝗹𝗱 𝗺𝗲𝗮𝗻 𝗳𝗼𝗿 𝘆𝗼𝘂𝗿 𝗳𝗮𝗰𝗶𝗹𝗶𝘁𝘆.

CURIS System: Innovating the future of biodecontamination

👉 Read the blog:
https://curissystem.com/resources/blog/the-vphp-myth-is-high-concentration-hydrogen-peroxide-really-better-than-low-concentration-h2o2

08/13/2025

CURIS Academy is out with a new Tip Series: This series will focus on MAL spaces

𝗧𝗶𝗽 #𝟭
𝘔𝘢𝘯𝘶𝘢𝘭 𝘥𝘦𝘤𝘰𝘯𝘵𝘢𝘮𝘪𝘯𝘢𝘵𝘪𝘰𝘯 𝘮𝘢𝘺 𝘣𝘦 𝘤𝘰𝘴𝘵𝘪𝘯𝘨 𝘮𝘰𝘳𝘦 𝘵𝘩𝘢𝘯 𝘺𝘰𝘶 𝘳𝘦𝘢𝘭𝘪𝘻𝘦

Create efficient workflows and ensure consistent efficacy every time, with CURIS' automated, integrated systems delivering reliable, repeatable >6-log sporicidal results.

Learn more about CURIS' customized or retrofit chambers:
https://lnkd.in/ebd3NXaK

08/03/2025

🔬 Headed to the *MABioN Annual Biosafety Symposium* this year?
So are we!

Stop by the CURIS System table and connect with Will Knapp, our Principal Contamination Control Strategist: He’ll be on hand to discuss cutting-edge solutions in biodecontamination and biosafety strategy - and how CURIS is supporting labs and facilities in creating safer environments.

This event is a fantastic opportunity for biosafety professionals to network, share, and learn. Whether you're attending to stay ahead in your field or to explore new tools, we’d love to meet you.

📍 See you at the table!

07/29/2025

We hope you plan to join Beth as she shares her extensive experience and from-the-field insights when she presents "𝙁𝙧𝙤𝙢 𝙀𝙛𝙛𝙞𝙘𝙞𝙚𝙣𝙘𝙮 𝙩𝙤 𝙀𝙛𝙛𝙞𝙘𝙖𝙘𝙮: 𝙄𝙣𝙣𝙤𝙫𝙖𝙩𝙞𝙤𝙣𝙨 𝙎𝙝𝙖𝙥𝙞𝙣𝙜 𝘽𝙞𝙤-𝙙𝙚𝙘𝙤𝙣𝙩𝙖𝙢𝙞𝙣𝙖𝙩𝙞𝙤𝙣 𝙞𝙣 𝙏𝙧𝙖𝙣𝙨𝙛𝙚𝙧 𝙀𝙣𝙫𝙞𝙧𝙤𝙣𝙢𝙚𝙣𝙩𝙨" at the 𝗣𝗵𝗮𝗿𝗺𝗮𝗘𝗗 𝗔𝘀𝗲𝗽𝘁𝗶𝗰 𝗣𝗿𝗼𝗰𝗲𝘀𝘀𝗶𝗻𝗴 𝗦𝘂𝗺𝗺𝗶𝘁 𝟮𝟬𝟮𝟱.

Here is a brief overview of what she will cover:

As use of automated biodecontamination continues to expand, pharmaceutical manufacturers’ concerns about challenges associated with traditional methods, such as material degradation, prolonged aeration times, and staff safety have grown, as well.

This presentation covers the latest breakthroughs in integrated biodecontamination systems for material transfer environments in pharmaceutical and research facilities. 𝘋𝘳𝘢𝘸𝘪𝘯𝘨 𝘧𝘳𝘰𝘮 𝘴𝘵𝘶𝘥𝘪𝘦𝘴 𝘤𝘰𝘯𝘥𝘶𝘤𝘵𝘦𝘥 𝘢𝘵 𝘱𝘩𝘢𝘳𝘮𝘢𝘤𝘦𝘶𝘵𝘪𝘤𝘢𝘭 𝘮𝘢𝘯𝘶𝘧𝘢𝘤𝘵𝘶𝘳𝘪𝘯𝘨 𝘭𝘰𝘤𝘢𝘵𝘪𝘰𝘯𝘴 𝘢𝘤𝘳𝘰𝘴𝘴 𝘵𝘩𝘦 𝘜𝘚, 𝘸𝘦 𝘸𝘪𝘭𝘭 𝘦𝘹𝘱𝘭𝘰𝘳𝘦 𝘵𝘩𝘦 𝘪𝘮𝘱𝘭𝘦𝘮𝘦𝘯𝘵𝘢𝘵𝘪𝘰𝘯 𝘰𝘧 𝘯𝘰𝘷𝘦𝘭 𝘴𝘺𝘴𝘵𝘦𝘮𝘴 𝘪𝘯 𝘣𝘰𝘵𝘩 𝘶𝘱𝘴𝘵𝘳𝘦𝘢𝘮 𝘢𝘯𝘥 𝘥𝘰𝘸𝘯𝘴𝘵𝘳𝘦𝘢𝘮 𝘵𝘳𝘢𝘯𝘴𝘧𝘦𝘳 𝘴𝘱𝘢𝘤𝘦𝘴, 𝘸𝘪𝘵𝘩 𝘢 𝘧𝘰𝘤𝘶𝘴 𝘰𝘯 𝘵𝘩𝘦𝘪𝘳 𝘢𝘣𝘪𝘭𝘪𝘵𝘺 𝘵𝘰 𝘮𝘢𝘪𝘯𝘵𝘢𝘪𝘯 𝘦𝘧𝘧𝘪𝘤𝘢𝘤𝘺 𝘸𝘪𝘵𝘩𝘰𝘶𝘵 𝘤𝘰𝘮𝘱𝘳𝘰𝘮𝘪𝘴𝘪𝘯𝘨 𝘴𝘵𝘢𝘧𝘧 𝘴𝘢𝘧𝘦𝘵𝘺 𝘰𝘳 𝘤𝘰𝘮𝘱𝘢𝘵𝘪𝘣𝘪𝘭𝘪𝘵𝘺 𝘸𝘪𝘵𝘩 𝘴𝘦𝘯𝘴𝘪𝘵𝘪𝘷𝘦 𝘦𝘲𝘶𝘪𝘱𝘮𝘦𝘯𝘵 𝘰𝘳 𝘮𝘢𝘵𝘦𝘳𝘪𝘢𝘭𝘴.

The discussion will include:

✅ A review of microbial decontamination challenges in different use cases for pharmaceutical and research facilities.

✅ Results from the automated system’s operation, including cycle times, microbial efficacy, and material impact.

✅ Best practices for implementing an integrated biodecontamination system for transfer spaces.

𝘛𝘩𝘦 𝘴𝘵𝘶𝘥𝘪𝘦𝘴 𝘩𝘪𝘨𝘩𝘭𝘪𝘨𝘩𝘵 𝘵𝘩𝘦 𝘱𝘰𝘵𝘦𝘯𝘵𝘪𝘢𝘭 𝘧𝘰𝘳 𝘪𝘯𝘵𝘦𝘨𝘳𝘢𝘵𝘦𝘥 𝘴𝘺𝘴𝘵𝘦𝘮𝘴 𝘵𝘰 𝘴𝘵𝘳𝘦𝘢𝘮𝘭𝘪𝘯𝘦 𝘰𝘱𝘦𝘳𝘢𝘵𝘪𝘰𝘯𝘴, 𝘮𝘪𝘯𝘪𝘮𝘪𝘻𝘦 𝘤𝘰𝘯𝘵𝘢𝘮𝘪𝘯𝘢𝘵𝘪𝘰𝘯 𝘳𝘪𝘴𝘬𝘴, 𝘢𝘯𝘥 𝘱𝘳𝘰𝘷𝘪𝘥𝘦 𝘢 𝘤𝘰𝘯𝘴𝘪𝘴𝘵𝘦𝘯𝘵, 𝘳𝘦𝘭𝘪𝘢𝘣𝘭𝘦 𝘴𝘰𝘭𝘶𝘵𝘪𝘰𝘯 𝘧𝘰𝘳 𝘣𝘪𝘰𝘥𝘦𝘤𝘰𝘯𝘵𝘢𝘮𝘪𝘯𝘢𝘵𝘪𝘰𝘯. 𝘉𝘺 𝘱𝘳𝘦𝘴𝘦𝘯𝘵𝘪𝘯𝘨 𝘳𝘦𝘢𝘭-𝘸𝘰𝘳𝘭𝘥 𝘥𝘢𝘵𝘢, 𝘵𝘩𝘪𝘴 𝘴𝘦𝘴𝘴𝘪𝘰𝘯 𝘢𝘪𝘮𝘴 𝘵𝘰 𝘱𝘳𝘰𝘷𝘪𝘥𝘦 𝘧𝘢𝘤𝘪𝘭𝘪𝘵𝘺 𝘮𝘢𝘯𝘢𝘨𝘦𝘳𝘴, 𝘲𝘶𝘢𝘭𝘪𝘵𝘺 𝘦𝘯𝘨𝘪𝘯𝘦𝘦𝘳𝘴, 𝘱𝘳𝘰𝘤𝘦𝘴𝘴 𝘦𝘯𝘨𝘪𝘯𝘦𝘦𝘳𝘴, 𝘢𝘯𝘥 𝘰𝘱𝘦𝘳𝘢𝘵𝘪𝘰𝘯𝘢𝘭 𝘭𝘦𝘢𝘥𝘦𝘳𝘴 𝘸𝘪𝘵𝘩 𝘱𝘳𝘢𝘤𝘵𝘪𝘤𝘢𝘭 𝘪𝘯𝘴𝘪𝘨𝘩𝘵𝘴 𝘪𝘯𝘵𝘰 𝘰𝘱𝘵𝘪𝘮𝘪𝘻𝘪𝘯𝘨 𝘣𝘪𝘰𝘥𝘦𝘤𝘰𝘯𝘵𝘢𝘮𝘪𝘯𝘢𝘵𝘪𝘰𝘯 𝘴𝘵𝘳𝘢𝘵𝘦𝘨𝘪𝘦𝘴 𝘪𝘯 𝘢𝘴𝘦𝘱𝘵𝘪𝘤 𝘦𝘯𝘷𝘪𝘳𝘰𝘯𝘮𝘦𝘯𝘵𝘴.

07/24/2025

𝗣𝗵𝗮𝗿𝗺𝗮 𝗠𝗮𝗻𝘂𝗳𝗮𝗰𝘁𝘂𝗿𝗶𝗻𝗴 | 𝗖𝗹𝗲𝗮𝗻𝗿𝗼𝗼𝗺𝘀 | 𝗖𝗼𝗺𝗽𝗹𝗶𝗮𝗻𝗰𝗲

Regulatory observations related to cleaning and disinfection are increasingly common during FDA inspections.

𝙄𝙣 𝙩𝙝𝙚 𝙢𝙤𝙨𝙩 𝙧𝙚𝙘𝙚𝙣𝙩 𝙖𝙧𝙩𝙞𝙘𝙡𝙚 𝙛𝙧𝙤𝙢 𝘾𝙐𝙍𝙄𝙎 𝘼𝙘𝙖𝙙𝙚𝙢𝙮, 𝙮𝙤𝙪'𝙡𝙡 𝙜𝙖𝙞𝙣 𝙞𝙣𝙨𝙞𝙜𝙝𝙩'𝙨 𝙨𝙪𝙘𝙝 𝙖𝙨:

💠 For facilities with production floors, cleanrooms, or fill-finish equipment, inadequate biodecontamination doesn’t just risk a Form 483—it can jeopardize product release, damage company reputation, and lead to costly remediation or lost contracts.

💠 Real-life examples where pharma manufacturers failed to align with cGMP and Annex 1 expectations

💠 How to avoid common pitfalls like unvalidated disinfectants and incomplete documentation

💠 How to protect SISPQ with safer, validated HHP™ v***r and full-cycle data traceability

𝗗𝗼𝗻’𝘁 𝘄𝗮𝗶𝘁 𝗳𝗼𝗿 𝗮𝗻 𝗙𝗗𝗔 𝗙𝗼𝗿𝗺 𝟰𝟴𝟯 𝘁𝗼 𝗶𝗱𝗲𝗻𝘁𝗶𝗳𝘆 𝘆𝗼𝘂𝗿 𝗰𝗼𝗻𝘁𝗮𝗺𝗶𝗻𝗮𝘁𝗶𝗼𝗻 𝗰𝗼𝗻𝘁𝗿𝗼𝗹 𝗴𝗮𝗽𝘀: 𝗦𝗽𝗲𝗮𝗸 𝘄𝗶𝘁𝗵 𝗮 𝗖𝗨𝗥𝗜𝗦 𝗖𝗼𝗻𝘁𝗮𝗺𝗶𝗻𝗮𝘁𝗶𝗼𝗻 𝗖𝗼𝗻𝘁𝗿𝗼𝗹 𝗦𝗽𝗲𝗰𝗶𝗮𝗹𝗶𝘀𝘁 𝘁𝗼 𝗹𝗲𝗮𝗿𝗻 𝗵𝗼𝘄 𝘆𝗼𝘂 𝗰𝗮𝗻 𝗽𝗿𝗼𝗮𝗰𝘁𝗶𝘃𝗲𝗹𝘆 𝗶𝗻𝘁𝗲𝗴𝗿𝗮𝘁𝗲 𝗯𝗶𝗼𝗱𝗲𝗰𝗼𝗻𝘁𝗮𝗺𝗶𝗻𝗮𝘁𝗶𝗼𝗻 𝘀𝘆𝘀𝘁𝗲𝗺𝘀 𝗼𝗿 𝗲𝘅𝗽𝗲𝗿𝘁 𝘀𝗲𝗿𝘃𝗶𝗰𝗲𝘀 𝗶𝗻𝘁𝗼 𝘆𝗼𝘂𝗿 𝗳𝗮𝗰𝗶𝗹𝗶𝘁𝘆.

Contact CURIS and let's get started!
1-800-928-8708

avoiding FDA warning letters due to inadequate biodecontamination and contamination control

07/03/2025

As we reach the midpoint of shutdown season, it's critical to ensure your decontamination processes are efficient, validated, and aligned with regulatory standards.

CURIS Biodecontamination Services delivers rapid, high-efficacy response for contamination events, changeovers, routine preventive maintenance, and planned or unplanned shutdowns.

Ideal for...Whole Labs | Equipment | Customized Solutions.

Using hybrid hydrogen peroxide™ biodecontamination technology, CURIS ensures VALIDATED EFFICACY and MINIMAL OPERATIONAL DISRUPTION.

Contact a CURIS service consultant today to learn why industry leaders trust CURIS for their biodecontamination needs.
𝟴𝟬𝟬.𝟵𝟮𝟴.𝟴𝟳𝟬𝟴

CURIS Biodecontamination Services: Raise your expectations

06/27/2025

Engineered to support GMP-compliant operations, the CURIS 3 adapts to the evolving needs of laboratory and pharmaceutical manufacturing settings, enabling validated, on-demand contamination control across critical environments.

Learn why so many are turning to CURIS for dependable biodecontamination solutions - speak with a specialist today: 1-800-928-8708

What will CURIS do for you?

CURIS 3: https://lnkd.in/eqiEE9xZ

06/19/2025

🚨 Complex equipment contamination? Traditional disinfection might not cut it.

From lyophilizers to IVC racks and underdeck spaces, CURIS Biodecontamination Services deliver comprehensive, low-concentration hydrogen peroxide disinfection—fast, effective, and safer for your sensitive equipment.

When equipment isn’t easy to reach or disinfect, we step in with proven expertise.

🔬 Tailored service. Sporicidal results. Minimal downtime.
👉 Request a Quote

CURIS Biodecontamination Services: Raise your expectations

Interested in learning what in-house biodecontamination would entail for your specific needs? Speak with a specialist today to discuss your options:
📞 800-928-8708

06/16/2025

Choosing the right biodecontamination solution directly impacts product integrity, compliance, and operational efficiency.

But finding a fumigation system that fits your specific needs takes more than guesswork.

✅ Schedule a personalized demo with a CURIS product specialist today and determine the optimal solution for your facility: Your product, and your people, deserve nothing less. 1-800-928-8708

CURIS System: Innovating the future of biodecontamination

05/22/2025

𝗔𝗿𝗲 𝘆𝗼𝘂 𝘀𝘁𝗶𝗹𝗹 𝗿𝗲𝗹𝘆𝗶𝗻𝗴 𝗼𝗻 𝗼𝘂𝘁𝗱𝗮𝘁𝗲𝗱 𝗱𝗲𝗰𝗼𝗻 𝗺𝗲𝘁𝗵𝗼𝗱𝘀 𝗳𝗼𝗿 𝗺𝗮𝘁𝗲𝗿𝗶𝗮𝗹 𝘁𝗿𝗮𝗻𝘀𝗳𝗲𝗿? 𝗟𝗲𝗮𝗿𝗻 𝘁𝗼 𝗮𝘂𝘁𝗼𝗺𝗮𝘁𝗲 𝗶𝘁.

𝙅𝙤𝙞𝙣 𝙪𝙨 𝙛𝙤𝙧 𝙖 𝙛𝙧𝙚𝙚 30-𝙢𝙞𝙣𝙪𝙩𝙚 𝙬𝙚𝙗𝙞𝙣𝙖𝙧 𝘵𝘰 𝘦𝘹𝘱𝘭𝘰𝘳𝘦 𝘩𝘰𝘸 𝘢𝘶𝘵𝘰𝘮𝘢𝘵𝘦𝘥 𝘥𝘦𝘤𝘰𝘯𝘵𝘢𝘮𝘪𝘯𝘢𝘵𝘪𝘰𝘯 𝘰𝘧 𝘔𝘢𝘵𝘦𝘳𝘪𝘢𝘭 𝘈𝘪𝘳𝘭𝘰𝘤𝘬𝘴 (𝘔𝘈𝘓𝘴) 𝘤𝘢𝘯 𝘪𝘮𝘱𝘳𝘰𝘷𝘦 𝘤𝘭𝘦𝘢𝘯𝘳𝘰𝘰𝘮 𝘪𝘯𝘵𝘦𝘨𝘳𝘪𝘵𝘺 - 𝙬𝙞𝙩𝙝𝙤𝙪𝙩 𝙩𝙝𝙚 𝙙𝙧𝙖𝙬𝙗𝙖𝙘𝙠𝙨 𝙤𝙛 𝙨𝙥𝙧𝙖𝙮 𝙖𝙣𝙙 𝙬𝙞𝙥𝙚.

'𝗖𝗼𝗻𝘁𝗮𝗺𝗶𝗻𝗮𝘁𝗶𝗼𝗻 𝗖𝗼𝗻𝘁𝗿𝗼𝗹 𝗦𝘁𝗿𝗮𝘁𝗲𝗴𝗶𝗲𝘀 𝘁𝗼 𝗔𝘂𝘁𝗼𝗺𝗮𝘁𝗲 𝘆𝗼𝘂𝗿 𝗠𝗮𝘁𝗲𝗿𝗶𝗮𝗹 𝗧𝗿𝗮𝗻𝘀𝗳𝗲𝗿 𝗗𝗲𝗰𝗼𝗻 𝗳𝗿𝗼𝗺 𝗡𝗼𝗻-𝗖𝗹𝗮𝘀𝘀𝗶𝗳𝗶𝗲𝗱 𝘁𝗼 𝗚𝗿𝗮𝗱𝗲 𝗔 𝗦𝗽𝗮𝗰𝗲𝘀' - presented by 𝗘𝗹𝗶𝘇𝗮𝗯𝗲𝘁𝗵 𝗠𝗮𝘀𝘀𝗼𝘁𝗵, 𝗦𝗠𝗘

During this session, you’ll discover:

✔️ Common contamination pitfalls and how to avoid them

✔️ How automated MAL decon accelerates throughput and eases compliance

✔️ Replacing your current chamber may not be necessary *

* Many CURIS customers have chosen to retrofit their outdated decon chambers with 𝗖𝗨𝗥𝗜𝗦 𝗠𝗼𝗱𝘂𝗹𝗮𝗿 𝗜𝗻𝘁𝗲𝗴𝗿𝗮𝘁𝗲𝗱 𝗦𝗼𝗹𝘂𝘁𝗶𝗼𝗻𝘀 - avoiding demolition, gaining material compatibility, 𝘢𝘯𝘥 reclaiming critical space without sacrificing efficacy

𝗣𝗹𝗲𝗮𝘀𝗲 𝗷𝗼𝗶𝗻 𝘂𝘀 𝘁𝗼 𝗱𝗶𝘀𝗰𝘂𝘀𝘀 𝗳𝗼𝗿𝘄𝗮𝗿𝗱-𝘁𝗵𝗶𝗻𝗸𝗶𝗻𝗴 𝗰𝗼𝗻𝘁𝗮𝗺𝗶𝗻𝗮𝘁𝗶𝗼𝗻 𝗰𝗼𝗻𝘁𝗿𝗼𝗹 𝘀𝘁𝗿𝗮𝘁𝗲𝗴𝗶𝗲𝘀; 𝗯𝘂𝗶𝗹𝘁 𝗳𝗼𝗿 𝘁𝗼𝗱𝗮𝘆’𝘀 𝗰𝗹𝗲𝗮𝗻𝗿𝗼𝗼𝗺 𝗱𝗲𝗺𝗮𝗻𝗱𝘀 𝗮𝗻𝗱 𝗮𝗱𝗮𝗽𝘁𝗮𝗯𝗹𝗲 𝗳𝗼𝗿 𝘁𝗼𝗺𝗼𝗿𝗿𝗼𝘄'𝘀.

🗓 𝗗𝗮𝘁𝗲: 𝗧𝗵𝘂𝗿𝘀𝗱𝗮𝘆, 𝗠𝗮𝘆 𝟮𝟵𝘁𝗵

🕦 𝗧𝗶𝗺𝗲: 𝟭𝟭:𝟯𝟬 𝗔𝗠 – 𝟭𝟮:𝟬𝟬 𝗣𝗠 𝗘𝗦𝗧

🎤 𝗦𝗽𝗲𝗮𝗸𝗲𝗿: 𝗘𝗹𝗶𝘇𝗮𝗯𝗲𝘁𝗵 𝗠𝗮𝘀𝘀𝗼𝘁𝗵, 𝗦𝗠𝗘

𝘘&𝘈 𝘧𝘰𝘭𝘭𝘰𝘸𝘪𝘯𝘨 𝘱𝘳𝘦𝘴𝘦𝘯𝘵𝘢𝘵𝘪𝘰𝘯

Register to attend:
https://lnkd.in/eEzY9Umk