Dear valued user,
Thank you for using Clearpol. Your support has been invaluable to us and we truly appreciate it. We launched Clearpol two years ago and thousands of users like you have joined us in our mission to simplify healthcare compliance. During the pandemic, we put Clearpol out for free as our way of helping, so you could focus on taking care of your residents.
Listen to our origin story here
As we move forward, we are determined to empower you with cutting-edge AI-enabled tools that will make managing compliance effortless. To bring this vision to life we've partnered with UC Berkeley, a leader in public health and AI research. We will also launch a PRO subscription starting March 1st to ensure the sustainability of Clearpol and to continuously improve the platform for all users. After March 1st, many existing, new, and future features will require a PRO subscription.
As a token of appreciation, we will be offering early adopters, students, and other special users the opportunity to be grandfathered in at an incredibly steep discount. Look out for future communications if you fall into that category.
Thank you for your understanding and continued support. We look forward to serving you in the future.
Best regards,
The Clearpol Team
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The information provided is used to show regulations that are relevant to your region/facility. By using the platform you agree to the terms and conditions.
Clearpol Inc. does not make any guarantees regarding the accuracy of the opinions provided on our platform. Please use your own judgement.
A new legislation, AB 818, effective from January 1, 2010, prohibits the use of an epidural, intravenous, or enteral feeding connection that would fit into another connection port unless an emergency or urgent situation exists and the prohibition would impair the ability to provide healthcare. The prohibition on epidural connection would commence 36 months after the publication of new epidural connection design standards by the International Organization for Standardization (ISO) or January 1, 2014, whichever occurs first. The prohibition on intravenous and enteral feeding connection would commence 24 months after the publication of new intravenous and enteral feeding connection design standards by the ISO or January 1, 2013, whichever occurs first. Health facilities licensed under HSC Sections 1250(a), (b), (c), or (f) are required to include patient safety plan measures to prevent adverse events associated with misconnecting intravenous, enteral feeding, and epidural lines in their patient safety plans.
Clearpol Inc. does not make any guarantees regarding the accuracy of the opinions or summaries provided on our platform. Please use your own judgement.
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