Cockpit Crew Blog

Welcoming Summer Intern Isaac Macrae

Cognition is excited to welcome Isaac Macrae to our Summer Internship Program. Each year, we accept a handful of students looking for real world experience in the sales, marketing, engineering, or development worlds. In total for summer 2017, we have invited three interns into the program, all landing in the development department.

Isaac Macrae

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The Implications of WannaCry on Medical Devices: How Interconnected Devices Can Exacerbate Cyber Attacks

Ransomware can be frightening. It holds all the data in a device hostage until the victim pays a sum of money, and even then, there is no guarantee the data will return. To be more specific, ransomware takes advantage of a security flaw and locks the user out until said ransom is paid. Initially, over 200,000 victims were affected by the recent WannaCry attack worldwide, which exploited a flaw in Microsoft Windows 7 and demanded a ransom in Bitcoin. Worryingly, WannaCry infiltrated the computer systems of London hospitals. WannaCry even took its first medical device hostages in the US during the major attack. This is the heart of things: connected medical devices, on these networks, can expose them to risk if they're not well protected.

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4 Benefits of Agile Product Development in the Medical Device Industry

Agile is an umbrella term for several iterative and incremental software development methodologies. Each one is unique in its approach; however, they all share a common set of core values which incorporate continuous feedback, planning, testing, and integration of the project and software used to facilitate the this process. It is, simply, a way to organize information efficiently when developing a product. It can be applied to product development outside of software as well.

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Sean Berube's Internship Overview

This week, we say goodbye to our latest Marketing intern, Sean Berube. He is in his final year at UMass Lowell, working towards his bachelor’s degree in English with minors in computer science and mathematics. On the side, Sean is a singer/songwriter, currently working on his latest song, “Royalties,” and hopes his future endeavors will allow him to explore music more. Sean wants to pursue a career in business, similar to what he experienced here at Cognition. He helped us write a good handful of blog and article material in his time here and we hope he will be coming back sometime to work with us again! We sat down to reflect with Sean about his time here with Cognition, figuring out what he learned and enjoyed.

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UMass Lowell’s 6th Biomanufacturing Summit 2017

Cognition was excited to co-sponsor UMass Lowell’s 6th Biomanufacturing Summit 2017 with industry giants and leaders such as Merck, Pfizer, Shire, Biogen, and FDA. The event was located at the elegant University of Massachusetts Club at One Beacon Street in Boston--the views were breathtaking, some of the best in the city. President and CEO of the Massachusetts Life Sciences Center, Travis McCready, kicked off the event with gusto.

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GAMP® 5 and why it's Relevant

Let’s take a look at GAMP® 5.

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AAMI TIR36, More Fun with Validation

The AAMI Technical Information Report (AAMI TIR36:2007) is a standard that covers the validation of software for regulated processes. TIR36 focuses on the machines, software, and processes involved with manufacturing devices and other products. Medical device engineer David A. Vogel lays out strategies for medical device companies in their automated process software validations, and includes a bit of history of multiple standards like TIR36, in Medical Device Software Verification, Validation and Compliance. He has first-hand experience with the standard as he and 13 other specialists in the field worked for about 3 years to establish TIR36, which is structured around the idea that there are multiple tools and approaches available, but only the ones that apply to each software element and its intended use should be used for validations. “The problem of validating non-device software is that it is so broadly defined that no single method or tool will work for all circumstances,” he says. This group published examples of validation plans to show how their methods could be applied, so now they have established some guidance.

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Biomanufacturing Summit 2017: Developing Your Company’s Next Breakthrough

Communication and networking are crucial for success in any field, and the biotech industry is no exception. The 2017 Biomanufacturing Summit, hosted by the Biomanufacturing Science and Technology Consortium (BSTC), Massachusetts BioManufacturing Center (MBMC) and UMass Lowell, is an opportunity for people in the biomanufacturing field to collaborate. The goal of the summit is to get professionals and leaders of the biotech industry to meet and discuss both current challenges in the field, and the best ways to develop breakthrough technology.

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Verification & Validation: A Necessary Activity

Verification & Validation (V&V) is a necessary step in every type of product development. Verification is a process of evaluating the development lifecycle to check if a team is on the right track of creating the final product. Validation is the process of evaluating the final product to check whether the software meets the business needs. Are we making the right product & Did we make the right product = V&V

Some customers coming to Cognition are confused by the guidelines surrounding verification and validation (V&V) work, or they say it was too difficult or time-consuming back when they started a particular project because of the methods or tools (or lack thereof) they had. They show us their 483 citations or are in need of heavy remediation, situations they could have avoided if validation was addressed from the start. Those situations can be really expensive. “Remediation costs represent 0.4 to 0.7 percent of annual sales” in medical devices, according to McKinsey & Company. With their estimate of annual sales of $380 billion, that adds up to $1.5-2.6 billion a year across the medical device industry.
                                                      
Good, efficient V&V work can be easier if the project is built well: not the product itself, but the structure of data collected about the product. A myriad of elements are involved. Is everything correctly traced? Is there an ongoing effort to produce clean, valid data? Is the company actually pulling together the elements to assemble a cohesive package, or are they setting themselves up for failure? Kunal Punjabi, a software expert from MindTheProduct, states that: “Ideally, building and validating the product should go hand-in-hand and be an iterative process, with some amount of validated learning along the way (or at the very least, with every iteration you make).”

Overall, V&V work is not easy and many workers do not enjoy doing it, but it is a necessity to achieve FDA approval. To learn more about how Cognition can help your company with their design controls V&V work, read the downloadable paper below!

Design Controls Series 5 Verification & Validation

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