Category Archives: Spotlight Interviews

Kuldip Singh Chiheru, Strategic GTM Head, Global Financial Services, Atos

A conversation with Kuldip Singh Chiheru, the Strategic GTM Head, at the Global Financial Services for Atos. 

Kuldip Singh ChiheruExperience • 2016-2017 Atos Strategic GTM Head – Loans
• 2015 – 2016 Atos FS Global Solutions Head
• 2012 – 2015 Global FS Bus Development Head 
• 2008 – 2012 Global FS Market leader
• 2001- 2008 KPMG & Atos KPMG FS Advisory
• 1997-2001 ICAP eTrading Program Lead
• Prior: HSBC Midland International Banking

Background
• BSC (Hons) Chemistry
• MSc Information Technology
• MBA Aston Business School

What do you hope the audience will learn from this webinar?

I hope that they understand the characteristics of a hyper competitive best class lending business model. Modern business solution design for agility and innovation and learning a business case for a best in class lending business. Another key note I hope the audience will learn from participating in this webinar is leveraging industrial scale deployment models for accelerating transformation.

For example, most financial organizations dream of launching new marketing offers or enabling a new partner channel  in seconds or adjusting lending processes in minutes. This can be the reality NOW. Rather than taking several months, and suffering extreme opportunity costs.

What discussions do you look forward to having with the audience?

I will be looking forward to discussing the investment priorities for Loans in next 1-2 years and a business case for the Retail Loan Factory for their priorities.

What do you enjoy most about your role?

The most satisfying aspect is helping customers transform their business and setting the target operating model benchmark for best in class for the next 15 years.

How did you get into the industry?

My passion for the industry grew even further when I was an International Banker with HSBC Midland.

Where is your favourite place in the world and why?

I have so many, each with their own unique attractions. The NW of India Punjab is very enlightening and the Canadian wilderness great for out door activities.

Don’t miss the chance to join Kuldip Singh Chiheru and Atos in their upcoming webinar ‘Lending Agility and Innovation For A Best in Class Digital Bank of the Future

Register Here! for this free webinar

Keith Howells – Senior Vice President of Development, OmniComm Systems

Data Collection, Clinical Trials and Healthcare:

A Conversation With Keith Howells, Senior Vice President-Development for OmniComm Systems

Keith HowellsMr. Howells has almost 25 years of experience in building and implementing applications that support clinical research. As head of development for OmniComm Systems, he is responsible for the TrialMaster product for Electronic Data Capture, and the TrialOne product for Phase I clinic automation. 

Prior experience includes 5 years as head of development for Medidata Solutions and 5 years as head of development for Oracle’s pharmaceutical application suite. Mr. Howells has a degree in physics from Oxford University, England.

Tell us a little about OmniComm; what does the company do?

OmniComm Systems, (OTCQX: OMCM), provides products and services that allow pharmaceutical and biotech companies to collect and manage clinical trials data. At first that sounds rather mundane – how hard can a data entry application be?

But in fact, the task is almost infinitely complicated and infinitely valuable. Whereas most web-based applications know in advance what data they wish to collect – Hertz.com knows you want to rent a car and Hotels.com knows you want a hotel room – we don’t know in advance what data is to be collected because every clinical trial is different.

Maybe the researchers are collecting blood pressure readings, maybe tumor measurements, maybe quality-of-life questionnaires, maybe all three. So we have to first supply a tool that allows customers to define their clinical trial; then we have to dynamically display the data-entry pages as if each had been lovingly crafted by hand. Those considerations, coupled with stringent regulatory requirements, make this a challenging and fascinating business.

In terms of the value, if we can save a month off the research time for a drug that becomes the next Humira, that month saved is literally worth a billion dollars. So we work hard to make sure our products are feature-rich and easy to use, and our service levels are highly responsive. There are a lot of vendors in this space, but we feel we have the right mix of robust capability and nimble responsiveness.

Why did you choose to hold this webinar?

It is remarkable how many different systems need the clinical data, whether for project management, payments to the investigative sites, safety reporting or data analysis. In today’s fast-paced world, you cannot afford a classical software development approach for each of these different data extract needs.

We’ve developed a number of generic approaches such that data may be extracted without programming, thereby providing a much more flexible and productive set of tools. We feel it is useful to share these techniques with interested members of the industry.

What do you hope the audience will learn from this webinar?

A number of the examples are based on our own technology, but we believe this webinar will provide value regardless of which data-collection system a company is actually using. We expect the audience to learn the generic mechanisms by which the raw data can be provided to the outside world, the kinds of re-formatting and manipulation that can be done on that raw data, and the standard mechanisms for extracting the data into other systems.

For example, safety reporting uses an international standard called E2B, and we’ll give a little insight into how that works and how the data is structured. It’ll be enough to educate some people and scare others!

What was your inspiration to get into the industry?

It was a total accident actually. When I was working for Oracle 30 years ago, the company split into servicing different vertical industries and there was no obvious choice for the pharmaceuticals vertical. So I bid for it. I had no idea what I was getting into, but the industry has proven uniquely fascinating, so I never left. It’s quite humbling to see the science and passion supporting the industry we serve, it’s an honor to be part of it, and obviously the mission brings a great sense of value. We’re not directly bringing life-saving products to market, but we’re helping the people who are.

What is the most rewarding aspect of your job?

We get to sit down at a computer screen and, out of thin air, create something that becomes a critical piece of other people’s lives. That’s pretty motivating.

Don’t miss the chance to join Keith and OmniComm in their upcoming webinar ‘Extracting Clinical Data for Reporting, Safety, SDTM & More’.

Jim Sinisgalli – Director of Market Development, UniSecure

Jim SinisgalliJim Sinisgalli is Director of Product Management – Brand Protection. He presently leads and guides Systech’s anti-counterfeit and authentication business to develop strategies which protect brands from counterfeit, diversion and other illicit trade.

He is responsible for developing and executing Systech’s authentication strategy working with leaders across products and services, and sales. Jim’s more than twenty-year career as a visionary leader includes half of his career spent protecting customers’ most precious assets from data to physical product.

Tell us a little about Systech International, what does the company do?

Systech is the global technology leader in product safety, and consumer and brand protection. In brief you could say that we pioneered serialization and are defining the future of authentication.

Offering revolutionary anti-counterfeiting technologies, authentication solutions, and supply chain data visibility applications, Systech makes customer’s brands more secure and the resulting data more accurate, valuable and actionable. As supply chains become more complicated and counterfeiting threats continue to grow, we will continue to be at the forefront of innovation.

How did you get into the industry?

Given Systech’s long history with vision/inspection solutions and being the first to introduce serialization, we have been on packaging lines for over 30 years.  We saw the capabilities of our solutions to take a barcode and be able to inspect it so closely we can differentiate between each and every one.  It was a natural fit to introduce this as a cutting edge anti-counterfeiting and brand protection solution.

Why did you choose to hold this webinar?

We try to collaborate and to engage with our customers wherever possible. Systech is in the middle of a very exciting time. Counterfeit products not only affect consumers but also result in huge losses for the manufacturing companies. We have experienced a great interest in UniSecure, our brand and product protection solution, and we have a lot of expertise that we can share, and solutions we believe would be useful to this community.

What are you looking forward to discussing with the audience?

It will be a great opportunity to brainstorm with the audience on leveraging their existing packaging, and the possibilities when we transform it into an anti-counterfeiting device.  Once you can identify each and every product, what can you do with that?

What is the most rewarding aspect of your job?

Systech has worked primarily with pharmaceuticals, our brand protection solution is popular in pharma, but introduces us to such a wide variety of other industries.  It is very rewarding to work and learn in these other market spaces to solve their pressing issues.

Be sure to  join Jim and Systech International in their upcoming webinar Protecting Your Brands Against Theft and Counterfeiting in 2017 and Beyond‘ . 

Ross Collins – Director, James Ross Consulting

Ross CollinsRoss Collins is a Director of James Ross Consulting, an independent global packaging consultancy operating from offices in the US, UK and Australia. Ross has over 30 years of experience in packaging engineering and project management and is a Fellow of the IOM3. He established James Ross Consulting in 1993 and since then the business has worked for major blue chip clients world-wide. Software development within James Ross Consulting began in response to a need for a next generation tool kit, one that would enable users to work collaboratively in developing solutions that were acceptable to marketing and optimized for the total supply chain. This provides clients with lowest cost / lowest footprint solutions for global markets.

What are you looking forward to explaining to the audience?

I am looking forward to explaining the genesis of PackDevPro and how the tool can drive better decision making within the NPD process and supply chain. This will provide direct cost and sustainability benefits for users and represents a new approach for packaging NPD.

Why did you decide to do a webinar with Business Review Webinars?

This is an exciting time for James Ross Consulting. We are officially launching our proprietary PackDevPro software and see this webinar as an opportunity to engage with the community it benefits.

PackDevPro has been critical to projects we have worked on in the past and we are looking forward to sharing its benefits as well our expertise with this community.

How did you get into the industry and what do you most enjoy about your role?

I am one of I am sure many ‘accidental technologists’ who ended up in packaging inadvertently. My original contact with packaging was in the pharma sector, where I worked on Quality Management initiatives – packaging seemed so much more interesting…the rest, as they say, is history. I think the most enjoyable aspect of the industry is the variety – packaging impacts marketing, design, cost, supply chain, engineering and operations – there is never a dull moment!

What are you hoping to achieve in the future in your personal and professional life?

Professionally, my goal is to establish James Ross Consulting as the leading force in packaging consultancy and to make it a benchmark for innovation and delivery of value for our clients. On a personal level, I am excited by the impact and potential that new technologies, like PackDevPro can bring to sustainability – we live in an age where technology is empowering and creating opportunities for us like never before.

Where is your favourite place in the world? I have been very lucky in being able travel a lot through working with James Ross Consulting – I have seen some great places and some not so great – but probably because of the travel home is always top of this list.

Join Ross Collins and James Ross Consulting discussing on their webinar entitled ‘Taking Control of Your Packaging‘ on 25th April.

Register Here!

Edward Benning – Smart Grid Integration & Security Lead – EMEA

EdwardEdward Benning Benning is Smart Grid Integration & Security Lead for EMEA at OMNETRIC Group. 

In this role, he leads a team focused on helping utilities asses the IT/OT convergence opportunity, create strategic integration roadmaps and implement solutions to optimize performance and fine-tune control of an increasingly complex grid. 

Edward has almost 20 years’ experience in the utilities consulting industry across Europe. He has worked in all facets of the utility industry including customer care and billing, smart metering, grid balance settlement, grid operations and analytics. His key strength is breaking down complex IT/OT challenges into achievable steps that deliver results. He has extensive experience in initiating and executing large scale IT/OT transformations as well in small innovation programs. 

What are you looking forward to explaining to the audience?

IT/OT integration is incredibly important to the utilities industry but its not easy, and while most are actively engaged in it, there is a wide variation in the progress that’s been made to date. My colleague, Jon Longstaff, and I are looking forward to explaining to the audience how to overcome the security concerns, interoperability challenges and cultural barriers that so often prevent utilities from reaping the benefits that integration can bring.

Why did you decide to do a webinar with Business Review Webinars?

TSOs and DSOs know that IT/OT integration is foundational to operating the distribution business of tomorrow, however there are many who are still at the strategy stage and have not got any further. At OMNETRIC Group we want to share what we’re doing to make integration easier, and talk about how to get a roadmap in place to help integrate processes, technology and information.

How did you get into the industry and what do you most enjoy about your role?

I started out in the utilities consulting industry almost 20 years ago, and have worked across all facets including  customer care and billing, smart metering, grid balance settlement, grid operations and analytics. I joined OMNETRIC Group from Accenture at its inception in 2014.

I particularly enjoy breaking down complex IT/OT challenges into achievable steps that deliver results. I also enjoy working with my team to initiate and execute anything from large scale IT/OT transformations to small innovation programs.

What are you hoping to achieve in the future in your personal and professional life?

I grew up, from a business perspective, in an IT world at Accenture. Then, when I started at OMNETRIC Group 3 years ago, I met electrical engineers and security experts with a deep knowledge and understanding of the operational technology that runs the grid.

Working with these folks has instilled in me the belief that, in the context of the smarter grid, systems integration should be approached from an operational perspective, and I want to build a team and a business to do just that.

Where is your favourite place in the world?

Work means that I currently spend most of my time in the UK, Belgium and Netherlands… so I’m happy to go to hotter climates for holidays towards the East.

Join Edward Benning and Omnetric Group in their webinar “Let’s Get Real: IT/OT Integration Approaches” on 21st March at 1PM London/9AM New York.

Register Here!

Mohammed Homman, CEO – Vironova AB, Sweden

by Mohammed Homman, CEO Vironova AB, SwedenMohammed Homman 800x673

Mohammed Homman is a dedicated entrepreneur with a degree in Biology from Uppsala University, Sweden and a Masters degree in Chemistry from the Karolinska Institute, Sweden. Mohammed developed ideas from his graduate research project in virology into the company, Vironova AB which he founded in 2005.

Image analysis software and a proprietary bench-top electron microscope system are at the heart of Vironova, that has now grown to 60 people and provides an instrument, software and expert consultancy solution.

Vironova was declared “one of the best start-ups of the year” in 2005, by the Swedish Government Agency for Innovation, VINNOVA. and Mohammed was honored with the Innovator of the Year award, by ALMI Stockholm.

Vironova AB has grown out of Mohammed’s passion for developing new ways to treat viral diseases and a need for objective viral and particle analysis. In a series of new companies, he has pursued various aspects of this goal.

Mohammed has continued to be recognized for his entrepreneurial and social skills, most recently in 2016 with the award from the King of Sweden of the “His Majesty Carl XVI Gustaf prize for remarkable entrepreneurial achievements”.

Tell us a little about Vironova, what does the company do?

In brief, you could say that we pioneer methods for nanoparticle analysis to turn the invisible into meaningful data.

We make electron microscopy available to the pharmaceutical industry through desk-top, user-friendly instrumentation and expert services in a regulatory environment. This gives our customers control over processes and quality and access to objective data when developing products using biologicals and nano-particles.

Vironova is alone in providing a complete package of hardware, software, services and systems in this area.

How did you get to where you are now?  

I founded Vironova in 2005 out of my own passion for studying viruses and finding new ways to treat viral diseases.

It was very problematic to have to use a massive electron microscope, count particles manually for hours and not have an objective or reproducible way to collect data from the images.

To solve the problem, I contacted people of many different specializations: microscopists, programmers, experts in imaging and image analysis etc. Bit by bit we built a whole system with a desktop transmission electron microscope (MiniTEM), proprietary software, services and consultancy. No other company offers anything like this.

So that all started 10 years ago but the need to collect meaningful data from electron microscopy in drug development is only growing. Biological structures (like viruses or liposomes) are being used more and more in drug delivery or as vaccines etc.

Why did you choose to hold this webinar?

We engage wherever possible with our customers –it’s through these discussions that we learn how to best serve them.

Vironova is in the middle of a very exciting time. Our new MinTEM system is on the market and we’ve experienced a great interest for it as there is a need for new solutions for sub-visible particle characterization in the biopharmaceutical industry.

We have a lot of expertise that we can share with this community, and solutions we believe would be useful to them.

What is the best thing about your job?

That’s easy! The chance to do something significant towards improving new drug development, healthcare and to move the virus field towards new solutions for viral diseases. We’re working on many fronts and growing steadily. There’s always something going on at Vironova, so it’s an exciting place to be.

Join Vironova for their webinar on Gene Therapy Vectors. Register now!

Paul Randall – Brand Innovation Manager, HP Inc.

Paul RPaul Randallandall is part of HP’s worldwide Brand Innovation Team. Working to support brands in their use of HP digital print technology to achieve efficiencies and cost savings as well as looking at how digital print can be a key innovation growth driver through delivering high impact consumer engagement campaigns. Having supported a number of projects that have used HP technology Paul has extensive knowledge of what it takes for digital print to be used successfully.

What do you hope the audience will learn from this webinar?

The webinar is a great opportunity to hear about yet another new way to bring product packaging to life with digital print and deliver “Brand Love” and experiential marketing via an instore experience. We hear so much about the changing consumer landscape that brands are faced with, and the evolving role of retail in delivering services to consumers as well as products. The technology we will showcase in this webinar provides an exciting solution to address these changes and ensure that brands can driver greater connections with their customer base.

What discussions do you look forward to having with the audience?

I truly hope this session drives excitement amongst the audience as they look at how this technology can apply to them and their businesses and their commercial goals moving forward.  Digital print is tool that enables brands to deliver on strategies through tactical packaging led activations that can truly bring success.

What do you enjoy most about your role?

What is most rewarding about my role is the way that we as HP are supporting brands to deliver projects that are ground-breaking. Every project we collaborate on always has a sense of new discovery and new achievements.

How did you get into the industry?

I got into this industry more by luck than judgement, as I’m sure is the case for so many people. But now here we are nearly 20 years further down the line and there is as much excitement and  innovation in the industry today as there was all those years ago.  I think we are fortunate to be involved in the packaging industry as it really offers so much scope for innovation and digital print technology is at the forefront of this. Whether it’s delivering cost efficiencies, or improving time to market or elevating the consumer experience and driving brand loyalty there is so much to admire about what our HP digital print technology brings to the industry.

Where is your favourite place in the world and why?

Ever since I was a child I’ve always been a sports fanatic. I spent so much of my early years involved in different sports and I now when i look back I realise those experiences have heavily influenced what I do nowadays and the people that I spend my time socialising with. So I probably relax and enjoy my time most when closest to a sports field of some description or another.  In recent times I’ve become heavily involved in coaching football to children and whilst maintaining the focus of 45 10 year old children on a sports field can be challenging is also delivers a great amount of personal satisfaction…… when things go right 🙂

Join Paul Randall and HP Inc. in their webinar “Delivering Customised Product Packaging Instore” in partnership with KOMDRUCK Printing Solutions on 5th April at 3PM London/10AM New York.

Register Now!

Sandra “SAM” Sather, VP, Clinical Pathways, Regulatory & Quality, TrialConsent – CRF Health

SAM White Background smile-014 - Web Sam’s current focus of consulting is to promote clinical quality systems for sponsors/CROs, investigators, and clinical research institutions. She has over 30 years of clinical experience, a Bachelor of Science degree in Nursing and a Master of Science degree in Education with a Specialization in Training and Performance Improvement. 

Sam has served many roles in clinical research, including site study coordinator and manager, sponsor and CRO monitor, quality assurance auditor, risk manager, trainer, and performance management consultant. She has held clinical research industry certifications for over 15 years by the Association for Clinical Research Professionals (ACRP). Sam is a current member of the ACRP Academy Board of Trustees and Regulatory Affairs Committee (RAC). She is a frequent subject matter expert for GCP regulation and speaker at industry conferences. Sam has authored dozens of competency-based curriculums for various clinical research stakeholders.

What do you hope the audience will learn from this webinar? We hope the audience will learn about the many ways that implementing an eConsent system can significantly support effective sponsor, investigator, and ethics committee oversight and eliminate many common informed consent deficiencies, e.g., wrong version used.

What discussions do you look forward to having with the audience? What do they perceive to be the barrier to eConsent? Commonly it is perceived cost, but this is not always the case. Comparing the manpower for development, oversight, and issues management that can be decreased with the solution, especially overtime, can actually save money.

What do you enjoy most about your role? As a clinical research consultant, I enjoy helping make the way we conduct research more effective and efficient.  I enjoy teaching about quality systems that ultimately better support human subject protection and data integrity.

How did you get into the industry? I was working as an RN in an intensive care unit where there were some clinical trials ongoing and I was the study coordinator.

Where is your favourite place in the world and why?  At home with my family in North Carolina.

Join Sandra “SAM” Sather, CRF Health & Chesapeake IRB in their webinar “Visibility and Oversight: What Paper Informed Consent Isn’t Offering You” on 23rd February at 3PM London/10AM New York.

Register Now!

Ronan O’Brien, Head of Business Development, Malvern Instruments Ltd.

Ronan O'BrienRonan O’Brien – Head of Business Development – Malvern MicroCal

Ronan has a PhD in biophysical chemistry and spent many years working in the area of label-free interaction analysis, a discipline in which he has published widely, including contributions to a number of educational textbooks.  He carried out his post-doctoral research with Professor Julian Sturtevant at Yale University and Professor John Ladbury at University College London, before joining MicroCal as an applications expert in 2001.  Since then he has held a number of roles including Scientific Marketing Manager and Head of R&D before taking on his current position as Head of Business Development for the MicroCal product group at Malvern Instruments.

What do you hope the audience will learn from this webinar? I hope that attendees will be excited to find out how these new systems, designed specifically for those working in the biopharmaceutical industry – particularly in biocomparability and similarity, manufacturing support, QC, process development, formulation development and candidate selection – will answer some of their key challenges and give them better data more quickly and easily. The webinar will be of real use to those who have an interest in stability testing of protein-based biologics.

What discussions do you look forward to having with the audience?

I would like to discuss ‘next steps’ – what else can we do to improve our products?  What annoys them or causes a bottleneck?  What do they love, and what could they not manage without? For that, we need constructive criticism from the audience! I would also like to hear about general ‘pain’ points in the industry, so that we can focus our innovation efforts in the right places to provide solutions that give genuine value to our customers.

What do you enjoy most about your role?

I love getting out of the office and travelling all over the world so that I can meet our customers, see what they do and listen to what they have to say.  That shows me the real value of what we do here at Malvern.  I also love the excitement of collaborating with customers to develop new technologies or features, then bringing those products to market and seeing the difference that our innovations make and the answers they provide.

How did you get into the industry?

Through my post-doctoral work, where I studied protein-ligand interactions and protein stability using biophysical tools, including microcalorimetry (Differential Scanning Calorimetry and Isothermal Titration Calorimetry)!

Where is your favourite place in the world and why?

I have two – is that OK? The first is my garden, because it’s peaceful, has an outlook onto the woods and is full of wildlife, and also my wife is at her happiest when she is there. The second is the Emirates Stadium in London – the home of Arsenal Football Club – because I’m a soccer/football nut and Arsenal is my team.

Join Ronan on February 21st for the webinar ‘Turning up the heat on protein stability characterization’ Register Here for the 10AM London session or Register Here for the 6PM London session

Eileen Dolan PhD, Professor of Medicine, Section of Hematology/Oncology, University of Chicago

eileen-dolan-ph-dDr. M. Eileen Dolan, Professor of Medicine, is Chair of the Committee on Clinical Pharmacology and Pharmacogenomics that includes a board-certified training program for clinical and post-doctoral fellows at the University of Chicago.

Within the University of Chicago Medicine Comprehensive Cancer Center, she serves as the Associate Director for Education and is co-leader of the Clinical and Experimental Therapeutics Program. She directs a Graduate Training Program in Breast Cancer Disparities including creating a graduate level course in breast cancer disparities. She recently received the University of Chicago BSD Distinguished Faculty Educator/Mentor award.

Her research is highly translational. She has a broad background in pharmacology, and specific expertise in pharmacogenomics of anticancer agent toxicity using both clinical genome wide association studies and preclinical studies to identify and functionally validate genes/genetic variants associated with adverse drug reactions.

She has recently developed cell-based methods using induced pluripotent stem cells to study chemotherapy induced peripheral neuropathy. She has over 200 peer-reviewed, original research publications and approximately 60 editorials/book chapters/reviews. Since 2000, she has been continuously funded in the area of pharmacogenomics and previous to that, held continuous funding for her work in DNA repair.

What is your primary field of study, and what motivated you to pursue this?

I have always been interested in finding ways to increase effectiveness and decrease toxicity of chemotherapy.  My primary field of study is pharmacogenomics of anticancer agent toxicity.  I investigate why some individuals are more susceptible for adverse effects of chemotherapy. I identify genetic and non genetic factors that result in some patients living with devastating side effects following treatment with curative therapy for their cancer.  I also
build cell based models to functionally validate signals from clinical genome wide studies of chemotherapy induced peripheral neuropathy and for drug screening of potential agents to treat neuropathy.

What do you enjoy most about your role?

Working as an academic scientists is a great career because we enjoy independence and can build teams of scientists to answer important questions.  We also wear several hats—educating through teaching or mentoring or building programs, research, administration. As long as we can get funding, we can work on questions that we are most passionate about.  My job is never boring: I am constantly learning from colleagues, students, and our staff.

What is your favourite part of presenting to a live audience?

I enjoy getting feedback and questions because that helps to elevate my science and consider other perspectives.  Presentations are an opportunity to organize results.

What are you looking forward to explaining to the audience?

I am going to discuss how we are using stem cell derived neurons to functionally validate genes identified in genome wide studies of chemotherapy induced peripheral neuropathy.  I will describe advantages of this model over existing methods and how the model has potential to be used to identify new drugs to prevent/treat this devastating side effect of chemotherapy.

Where is your favorite place in the world and why?

My favorite place in the world is Chicago because the skyline is beautiful, there are great restaurants, strong universities, major sports teams and a lovely lake front. I also have a large family that lives in Chicago. Today it is –10 degrees in Chicago, so today my favorite place is San Diego.

Join Eileen  on January 25th for the webinar “iPSC-derived Cell Models for Oncology Applications”. Register here!