CNA download - Certified Nurse Assistant Updated: 2023

Career Advancement: Stacking credentials with PaCE opens doors to higher-paying positions and more significant responsibilities within the healthcare administration field.

Increased Employability: Employers recognize the value of a multifaceted skill set. By stacking credentials, you position yourself as a well-rounded professional ready to tackle complex challenges.

Flexible Pathways: PaCE offers flexible scheduling and learning options, ensuring that you can balance your professional development with your existing commitments.

State

Zip Code

Country

The DeNovix CellDrop^™ Automated Cell Counter has achieved ACT^® Label certification from My Green Lab^®, making it the first automated cell counter accredited by the program.

The ACT Environmental Impact Factor Label provides third-party verification for the environmental impact of laboratory products. The label is designed to help scientists make more sustainable purchasing decisions, with scoring categories such as manufacturing, energy and water use, packaging, product content, and more.

Both CellDrop models (CellDrop BF and FL) received ACT Labels for the three geographical regions represented by the program: United States, Europe, and the United Kingdom. In the United States, the CellDrop BF scored 24.3 and the CellDrop FL scored 24.9. These scores are among the lowest in the ACT Label program, demonstrating the efforts made by DeNovix to minimize the environmental impact of our instruments.

A full breakdown of the scores is available at denovix.com/act-labels.

The ACT Label recognizes CellDrop’s innovative approach to cell counting, which removes a source of common plastic waste from laboratories. The instrument’s patented DirectPipette^™ technology allows users to load samples directly into a permanent chamber, thereby eliminating the need for plastic cell counting slides. This unique feature was identified during the formal review process and appears in the “Innovation” section of the label.

The CellDrop also scored favorably for its low energy consumption, sustainable packaging, direct shipping (for US orders), and expected 10+ year lifetime.

There’s been a real increase in the importance of sustainability when it comes to purchasing laboratory equipment... The ACT Label program is a great guide for helping scientists make better decisions, and we’re thrilled that CellDrop is a part of it. The label reflects the good work CellDrop has been doing to reduce single use plastics, as well as the actions DeNovix has made to Improve our sustainable practices.

Andrew Jones, DeNovix Market Development Manager

We congratulate DeNovix on their first ACT. labels for CellDrop... This innovative technology proves that there can be alternative approaches in the laboratory that make a real impact in reducing environmental impact. In this case, the complete removal of disposable plastic slides from the application together with the approaches to efficiency and sustainability in manufacturing and materials align with the core values of the ACT. Label program. We look forward to more positive collaboration with DeNovix.

Raj Patey, Business Development Director, ACT, My Green Lab

The DeNovix CellDrop Automated Cell Counter is available for labs to evaluate for free via the DeNovix Free Trial program. Contact DeNovix or a DeNovix Distributor for details.

LAS VEGAS, Oct. 26, 2023 /PRNewswire/ -- Blue Life Solutions, a pioneering contract medical device manufacturing company specializing in sample collection devices, announced the receipt of its ISO 13485:2016 certification. This achievement underscores the company's dedication to upholding the highest standards of quality, and ISO 13485:2016 certification serves as a pivotal milestone in Blue Life Solutions' mission to advance life-saving disease diagnostics.

ISO 13485 is a globally recognized standard that symbolizes an organization's steadfast commitment to quality, regulatory compliance, and the implementation of rigorous processes to ensure the safety and efficacy of medical devices.

"We are thrilled to announce our ISO 13485:2016 certification," stated Tarek Soubra, General Manager of Blue Life Solutions. "This milestone represents the culmination of our team's hard work and dedication to ensuring the utmost quality in our medical devices. It reaffirms our commitment to not only meeting but exceeding the expectations of healthcare providers and the patients they serve."

Blue Life Solutions' ISO 13485:2016 certification is a testament to the company's unwavering dedication to its customers, partners, and the patients they collectively serve. This achievement solidifies the company's position as a trusted and dependable partner in the medical device manufacturing industry. Achieving ISO 13485:2016 certification signifies Blue Life Solutions' dedication to the following core principles:

1. Quality Assurance: Blue Life Solutions places quality at the forefront of its operations, ensuring that its medical devices consistently meet or exceed industry standards.
2. Regulatory Compliance: The company is committed to adhering to all regulatory requirements, ensuring that its products meet the stringent criteria set by regulatory bodies.
3. Patient Safety: Blue Life Solutions prioritizes patient safety, designing and manufacturing medical devices with the highest levels of safety in mind.
4. Process Excellence: The ISO 13485:2016 certification attests to Blue Life Solutions' implementation of robust processes, ensuring the reliability and consistency of its products.

For more information about Blue Life Solutions, please visit www.bluelifesolutions.com.

About Blue Life Solutions:

Blue Life Solutions is a pioneering contract medical device manufacturing company dedicated to enhancing accessibility, optimizing workflows, and dismantling healthcare barriers with the mission to facilitate life-saving diseases diagnoses. Their specialization lies in DNA/RNA sample collection devices and In Vitro Diagnostic Devices. They offer automated reagent dispensing, custom packaging, labeling, and fulfillment services. Blue Life Solutions is a registered FDA facility, ISO 13485:2016 certified, and adheres to US 21 CFR Part 820 (cGMP) regulations.

For media inquiries, please contact: info@bluelifesolutions.com

View original content to download multimedia:https://www.prnewswire.com/news-releases/blue-life-solutions-achieves-iso-134852016-certification-strengthening-commitment-to-medical-device-excellence-301967979.html

SOURCE Blue Life Solutions

In order to get your driver’s license in Washington state, there are certain requirements you must meet. Of course, this includes passing your written and driving tests, as well as other necessities like proof of identity and vision screening.

There are also medical requirements to obtain a driver’s license in Washington state. When you apply for a drivers license, one of the questions on the application asks if you have any condition that could impair your ability to drive; answering this untruthfully is against the law. Your answer may prompt a required screening from a medical professional and a full medical certification to get a license.

Further, the Department of Licensing (DOL) can suspend or cancel your license based on certain medical conditions if they are a proven risk. For example, someone with epilepsy may have their license suspended over a latest loss of control over their condition or if someone with narcolepsy has a sudden onset of symptoms.

Unless otherwise stated, the information below comes from the Revised Code of Washington or the Washington State Department of Transportation.

WA driver’s license medical exceptions

Physicians and civilians in Washington can report drivers who are a potential safety risk by filling out a Driver Evaluation Request online. If there is sufficient reason to believe someone has an impacted driving ability, the DOL has the right to evaluate them.

Once the DOL is aware of a medical issue that can potentially impact driving, reexaminations for the driver in question will be required. This can include the written test, the driving test, new professional certification, or all of the above.

There are specific scenarios in which the Washington State Department of Licensing can cancel your license:

• Information received by the department shows your condition is not controlled

• Information received by the department shows your condition is not within licensing standards

• If you fail the reexamination of your driving skills

In other scenarios, the DOL can suspend your license but not cancel it:

• DOL does not receive certification in time

• DOL receives incomplete certification

• If you don’t complete the reexamination

• If you don’t show up for the reexamination

However, the DOL can also issue license restrictions based on a doctor’s report. This can include restrictions against driving at night for those with poor vision, vehicle type restrictions, and the approval of mechanical control devices, like those used by disabled drivers.

What is WA’s licensing standard?

Washington does not have a set list of medical conditions that ensure license prevention. Instead, certain conditions are considered a possible risk, and medical professionals evaluate the severity of symptoms.

While not an exhaustive list and other symptoms or conditions can be reported and evaluated using the same forms, the physical examination report asks about the following:

• Loss of consciousness or control or seizure

• Sleep apnea, narcolepsy, and other sleep disorders

• Dementia or other cognitive impairment

• Loss of muscular control or mobility

Medical professionals are asked to list the month and year of the most latest occurrence for the first two conditions and evaluate whether there has been a decline over the past 12 months for the second two.

The report asks the medical professional to determine if the condition could impact driving ability, if it is stable and controlled, or if it is controlled by medication that may also affect driving ability.

Based on the above assessments, doctors are asked for their professional opinion on whether an individual is able to operate a vehicle safely and if they believe the DOL should require continued evaluations. This can be recommended on a six-month, one-year or two-year basis.