When it comes to implementing mobile technologies at your company, there’s no one-size-fits-all approach. Over the years, there are four distinct methods of deploying mobile solutions in the enterprise that have emerged: BYOD, CYOD, COPE, and CLEO.
Download this whitepaper to learn what BYOD, CYOD, COPE, and CLEO mean, what are the benefits and challenges with each approach, and what are the best practices that other Life Sciences companies employ with managing mobility.
You know that mobile technologies can help field service technicians in the life sciences industry to be more efficient and productive as well as boost the company’s bottom line. However, it’s not enough simply to purchase several smartphones, tablets, or other mobile devices, give them to your field service techs, and hope for the best. Relying on a set of best practices when implementing mobile technologies makes the process much smoother – read on to learn what some of those best practices are.
The life sciences field has begun to embrace mobile technologies. Companies realize that it can make them more profitable and competitive. There are a number of ways in which mobile technologies can be implemented in this sector. This post will deal with how field service technicians in the life sciences field can become more efficient as a result of mobile technologies.
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The life sciences industry constantly produces cutting-edge, innovative solutions to help patients live longer, healthier lives. But when it comes to mobile technologies (a cutting-edge field in and of itself), life sciences firms still struggle with the same issues as other companies that aren’t as innovative. Mobile devices present opportunities as well as challenges. Certain mobile technology policies will work better than others. This post discusses the benefits, risks and challenges, and best practices of choose-your-own device (CYOD).
Bringing your own device (BYOD) to work has become commonplace in virtually every field and industry, and life sciences is no exception. For employees, BYOD is enormously freeing – they can use the devices they want when they want them. For IT departments and companies, BYOD can be a nightmare. There are significant security concerns and compliance issues to navigate regarding mobility. Read on to learn how life science firms can balance the benefits of BYOD with the risks and challenges through best practices.
When it comes to choosing a mobility policy for your company, you have several options. Your choices can be overwhelming, and it can seem as though you’re swimming in an alphabet soup. The process of identifying the right mobile technology policy for you doesn’t have to be daunting. Read on to learn more about why choose-your-own-device (CYOD) could be the best fit for your firm.
If you do an online search for the term “BYOD,” you’ll get two types of results. The first category will talk about how wonderful BYOD is, while the second will bemoan the security risk and burden BYOD creates for companies. BYOD is neither wholly good nor absolutely terrible – the reality is a bit more complex. Read on to learn about the benefits, risks, and best practices associated with BYOD.
For medical device manufacturers, success depends on cost-effectively maintaining regulatory compliance, driving rapid technological innovation, efficiently documenting quality data, managing product life cycles, and driving higher value to customers. It takes a lot risk management and continuous improvement to remain competitive in the face of these complex requirements.
Medical Device manufacturing companies operate in one of the most competitive – and regulated – industries today. Like many technology, electronics, and device manufacturing organizations, success in the Medical Device industry depends on a company's ability to produce the highest quality products faster than the competition. Unlike many other industries, however, Medical Device manufacturers must meet some of the most stringent government and customer compliance regulations regarding documentation, controlled processes, and product safety.
This requires more than medical device ERP or Quality Management software.
Sure, Medical Device companies need features like electronic device history records, CAPA, track and trace, recall procedures, learning management, document management, kitting and assembly, warranty and more. But all of these features mean nothing if your people do not accept change and adopt the system; your workstreams are inefficient; the solution is not validated or implemented correctly; or there is no foundation for continuously improving value to customers.
Therefore, it is extremely important that any Medical Device company looking to undertake an enterprise transformation project works with a proven consulting partner with expertise streamlining workstreams, mitigating risk, facilitating organizational adoption, and implementing compliant software solutions.
Merit Solutions enables Life Sciences organizations to transform their business with MAXLife, a robust and pre-configured Microsoft Dynamics AX solution that is deployed in the cloud using Microsoft Azure. MAXLife consists of pre-built business process models, industry-specific documentation, implementation templates, and integrations with top vendors – creating a preconfigured solution that can be “dropped in” with standard configurations or used as an “accelerator” for global deployments.
Learn more about MAXLife for Life Sciences.
Merit Solutions has been working with Life Sciences companies for more than a decade, helping them manage risk, ensure operating performance, maintain compliance, and pursue global growth opportunities. Through our industry-tested combination of front end process consultants, back end technology practitioners, and industry Subject Matter Experts, we have the expertise to enable your successful Life Sciences business transformation.
Our broad range of Life Sciences consulting services and IT solutions help address the challenges related to traditional processes, cultural resistance to change, and less scalable technologies – enabling successful improvement projects while operating in a globally regulated environment.
Life Sciences companies that partner with Merit Solutions typically experience the following results from their investments:
Merit Solutions helps our life sciences clients drive their business, process, and enabling systems changes required to achieve their strategic vision and goals. This includes everything from future state business process mapping to systems analysis, fit-gap process definition and scoping, sourcing, design and deployment, integration with other systems, on-going support, and systems validation.
(You are on our Microsoft Dynamics GP Advanced Lot Management Page. If you are interested in Enterprise ERP and Lot Management solutions – check out our Microsoft Dynamics AX Page for more information.)
Expand your ability to operate efficiently while controlling restricted materials within Microsoft Dynamics GP Manufacturing. Increase operating control, track all lot information completely, and automatically maintain compliance with FDA requirements.
Impose material use limits through Expiration Date field.
Control Lot Status with the addition of four status assignments: Hold, Approved, Quarantined and Rejected.
Manage lot transactions by only allowing use of approved materials in manufacturing and distribution.
Enforce rules for specific data choices and tolerances for lot characteristics.
Track Lot Information – Completely
Track lot information in key stages of inventory processing such as Manufacturing Order Receipt and Inventory Adjustments.
Works with Dynamics GP Inventory—Sales Order, Purchasing Order and Manufacturing Order Processing.
Maintain Compliance – Automatically
Advanced Lot Management is configurable to support your company-specific process and compliance rules.
Used with the Risk Management Suite, Advanced Lot Management operates in accordance with the requirements of FDA 21 CFR Part 11.
Contact Merit Solutions for more information on Advanced Lot Management.