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“The Future of Leave: Four Essentials Your Leave and Absence Management Strategy Needs Now”

Are you ready for the future of leave? Download the guide to see the four essentials your leave and absence management strategy needs now.

Employee leave and absence management is more complex than ever with evolving laws, regulations and employee needs. The recent pandemic has only accelerated the growing employee demand for stronger leave programs and increased time-consuming administrative burdens for employers and HR teams. Yesterday’s leave programs aren’t working for today’s workforce.

Many employers and HR teams are reassessing leave management, making a modern leave program a strategic imperative. Now is the time to take an innovative approach and streamline your leave administration and management – for a more efficient digital experience. The question left is: What does the future of leave look like for your business?

Download this guide to help you revolutionize your leave and absence management with information on

All the ways expectations for leave are changing and what that means for you.
The four essential characteristics of a future-forward leave management program.
How to decide on a strategy that will last.

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“Software Design for Medical Devices exclusive case studies, from over 16 industry leaders, including: MHRA, Siemens, Novartis, and Roche Diagnostics!”

Europe’s Only International Forum Dedicated to Medical Device Software Design and Compliance

Software design for medical devices is becoming subject to increased regulations, changing standards and evolving best practices. In order to help you keep up with this shifting landscape, Pharma-IQ is proud to present its 6th Annual Software Design for Medical Devices (SDMD)
conference!

SDMD 2016 will bring together 50+ professionals from across the medical device industry with the end goal of addressing their regulatory and technical challenges.

Join us at SDMD 2016 to:
* Discuss the proposed new European regulatory structure with insight from the MHRA
* Discover what novel practices and tools your peers (and
competitors) are using in their software development and validation with case studies from GE, Philips, Siemens, Drägerwerk and more
* Learn how to get the most out of a truly agile workflow in your projects with an innovative demonstration from an Agile Coach on ‘mob-programming’
* Develop basic-crypto techniques to increase product security with insight from Philips Healthcare
* Gain a better understanding of the Human Factors engineering process with help from Roche Diagnostics

Bringing together Software Engineers, Quality Assurance and Regulatory Managers, with an inspiring speaker panel and content that really addresses the challenges and issues on everyone’s mind right now. This event promises to be a platform for innovation and an incredible networking opportunity.

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“CollaborateMD vs. AdvancedMD EHR vs. InSync by Qualifacts Ratings Compared”

CollaborateMD or AdvancedMD EHR or InSync by Qualifacts–which is a better fit for your business? Both products may share some similar features and benefits; that’s why they’re so often compared to one another.

But each has its own pros and cons. And the differences between them could mean the success or failure of the tool for your business.

Download our report, and you’ll get:

Honest feedback from people who have used these tools.
Reviews from users who have scored the products on value, ease of use, and more.
A side-by-side comparison of each product’s ratings, including number of reviews.

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“Increasing Patient Engagement and Helping Clinical Trials Reach Full Potential with the Clinical Research as a Care Option Model”

Only 3% of people with cancer participate in clinical trials.

CRAACO seamlessly integrates clinical research with medical care, so more patients and physicians are able to contribute to the development of new treatments.

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“Hearing Health Care: More Choices, Better Outcomes”

Discover what consumers and hearing care providers are saying about the importance of extensive product choice within a health plan’s hearing benefit.

For health plan members with a hearing benefit, access to an extensive hearing aid formulary enables their hearing care providers to tailor a hearing solution to individual needs, preferences and lifestyle. It also helps satisfy the growing consumer demand for specific brands of hearing aids. However, the number of brands within a hearing aid formulary can vary significantly among the various hearing health care third-party administrators.

A white paper published by Amplifon Hearing Health Care dives into the results of two surveys that probed the perceptions of consumers and hearing care providers regarding the impact of product choice on hearing loss treatment. The white paper, titled “Hearing Health Care: More Choices, Better Outcomes,” includes discussion about:

Consumer views of their overall hearing health experience, importance of access to a wide range of hearing aid brands and desire to know their brand/product options before visiting a hearing care provider
Provider views of why it’s important to offer a broad selection of hearing aid options, specific patient benefits of extensive choice and level of satisfaction with the range of products available through health plan hearing benefits
The financial and health consequences of hearing aids that go unused or underutilized

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“How IoT is Transforming Health Care”

A look at how IoT devices are being deployed to improve patient care, and how the pandemic changed the technology’s status in the health care landscape. Responding to post-pandemic pressures, the health care industry is seeing rapid adoption of IoT devices in patient care and monitoring.

IoT continues to transform the sector as more patients and medical professionals turn to connected devices. From remote patient monitoring and data collection technologies to wearables and even ingestible sensors, IoT continues to revolutionize the health care industry and drive innovation.

In this special report from Scarlet Evans, we look at how IoT devices are being deployed to improve patient care, and how the pandemic changed the technology’s status in the health care landscape.

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“Advancing Automated Heat-Induced Epitope Retrieval”

HIER processes are more reproducible, less damaging to tissue sections, and save a great deal of time.

Formalin is a cross-linking type of fixative, forming methylene bridges between proteins within the tissue.This cross-linking reaction adversely alters the structure of tissue proteins, resulting in loss of antigenicity.One way to restore antigenicity is through the use of heat-induced epitope retrieval (HIER) prior to immunohistochemistry (IHC).

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“How Healthcare is Using AI to Automate Customer Experiences”

The healthcare industry has made rapid strides to innovate in response to changed market conditions and member and patient needs and expectations. Is your organization ready?

Customer expectations have changed, with COVID-19 forcing innovation at an accelerated rate to make experiences as self-service and user-friendly as possible. Regardless of what happens next in our “new normal”, this evolution must continue, centering increasingly around customer experiences powered by Artificial Intelligence (AI) and automation to increase member and patient satisfaction, relieve staff burden, and power more self-service.

Download this eBook to learn how:

Digital experiences are common and preferred among members and patients of all ages.
Healthcare companies are adopting AI-powered self-service to elevate customer satisfaction and reduce operating expenses.
Automating predictable customer touchpoints allows healthcare staff to focus their time on more complex activities.
Five experiences are simplified by augmenting live interactions with intelligent self-service

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“How to Use Risk-Based Monitoring and Clinical CAPA to Ensure Compliance”

If your company is a sponsor or a CRO that conducts clinical research for a sponsor, how effective are your risk management and clinical CAPA processes? Are you using a risk-based approach to monitoring and CAPA to mitigate the risks during clinical research and ensure compliance?

This white paper will discuss the importance of risk-based monitoring and CAPA in clinical research within the context of the following initiatives by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA):

2013 Guidance
Clinical Trial Transformation Initiative (CTTI)
EMA’s Reflection Paper on Risk-Based Quality Management in Clinical Trials

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“Redefining Telepharmacy: Unleash the Power of Your Pharmacy”

Get on the Grid with Telepharmacy 2.0

Telepharmacy today is not what it used to be. With recent advances in specialized software and integrated technology, telepharmacy workflow is now more sophisticated and optimized, delivering higher quality at a lower cost. By streamlining communications and processes, remote teams can serve as a true extension of your onsite team, creating opportunities for new operating models that can amplify the impact of pharmacy on patient care.

With the right pharmacy technology platform and management systems, telepharmacists can now perform all of the same tasks that in-house pharmacists perform. What’s more, the same innovative software can also be used by in-house staff to gain clinical and operational improvements from pharmacy-focused user interfaces and workflows, clinical decision support and alerts, and transparent reporting; and ensures continuity between onsite and remote pharmacists.

Download our eBook to learn about how telepharmacy can improve efficiency and operations throughout your entire facility.

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