Hear how brand owners can fight back against counterfeiting and other forms of illicit trade!
Join a live conversation with
Michigan State University’s School of Criminal Justice professor, Dr. Jeremy Wilson! Hear about Professor Wilson’s six building blocks or tenets, which provide “a framework for building and advancing brand protection programs that are strategic, comprehensive, and evidenced based.” We’ll talk with him about these tenets and about his forthcoming book,
Brand Protection and the Global Risk of Product Counterfeits: A Total Business Solution Approach, which is packed with brand protection learning, insights, and case studies from the field.
In this session, Jeremy will dive into:
- Latest industry insights based on network research
- Tactics to fight back against illicit trade
- Strategic organizations for effective brand protection
- “Total Business Solution” approach
To view a copy of the recording, click here.
Date Wednesday, January 26
Speakers:
- Frederic Menardo, Vice President EMEA (Excellis Europe)
- Sean O’Hearen, Managing Consultant and Global Brand Protection Specialist (Excellis)
Counterfeiting methods are becoming ever more sophisticated. As counterfeiters seek to exploit products entering new markets with fewer controls, serialisation compliance and brand security remain an ongoing challenge and the strength of pharma supply chains is frequently tested.
With patient safety and brand integrity a critical concern, managing and mitigating the growing risks of counterfeiting, tampering and trademark infringement in day-to-day operations is an essential component of safe and effective pharma product management.
In an age where the protection, security and traceability of medicines is constantly under the spotlight, pharma companies of all sizes must rise to the challenge of developing watertight systems and processes across their entire operation.
In this insightful hour-long FREE webinar, global pharma compliance specialists Excellis Health Solutions (part of NNIT) will explore these risks in greater detail, highlighting the key considerations every pharma company must address in 2022.
To view a copy of this webinar, please click here.
Managing EMVS EU-FMD alerts in a timely and GMP-compliant way is a legal obligation for every pharma manufacturer selling to the European market.
Over two years after go-live, it’s clear that this remains a challenge, and the volume of alerts – despite being reduced overall – will remain significant over the long-term.
Across the broad range of customers for whom Excellis operates the Alerts Management Service, we observe an alert rate of 3 alerts per 1,000 packs – making EU-FMD alerts a daily occurrence.
Every MAH therefore needs a solid, reliable, quality-compliant process, operating during EU pharmacy working hours to achieve the mandated response times – regardless of whether the alert’s source is caused by the MAH or more common supply chain factors beyond their control.
Join our Webinar to learn:
- What are your obligations?
- How can you manage your EU alerts in a compliant but lean way?
- How may the future EMVO AMS integrate with your process?
To view a copy of this webinar, please click here.
The Brazilian Authorities (ANVISA) have set out requirements in line with the National Medicine Control System (SNCM). Join Excellis as we talk about what that means for Pharma companies, and how you can get ready for the April 2022 deadline.
Date: January 28, 2021
Speakers:
- Christoph Krahenbuhl, Senior Director – Excellis Europe
- Volker Ditscher, Director Global Sales Track & Trace, WIPOTEC-OCS
After studying electrical engineering with a focus on automation technology, he worked in the automotive industry at General Motors. Since 2007 he is active for the WIPOTEC Group, the world market leader in Track & Trace systems for marking products in various industries with unique codes. As a Project Manager Mr. Ditscher lead several hundred such serialization projects. Since 2011 he is globally responsible as the Director Global Sales Track & Trace for the relevant product division at WIPOTEC-OCS.
- Marcelo Cozac, Director, MC Pack Equipamentos
Marcelo is an Engineer with 24 years experience in the packaging industry and 11 years experience in track and trace application for the Pharmaceutical Industry.
To view a copy of this webinar, please click here.
Global life science manufacturers are facing ever-increasing disruption in the markets they serve.
Join us as we launch a new 4-episode series focused on how to be an Adaptive Manufacturing Enterprise with speakers Bart Reitter, VP Life Sciences at QAD, Inc. and Greg Cathcart, CEO at Excellis. These 30-minute episodes will occur throughout November and December. Simply register for the series, receive one log-in link, and we’ll send you a reminder leading up to each event.
Featured Speakers:
- Bart Reitter, VP Life Sciences (QAD)
- Greg Cathcart, CEO (Excellis Health Solutions
Date/Time: December 15 @ 1PM EST
Episode 4: Digital Manufacturing – Leveraging technology in Life Sciences
Adaptive Manufacturing Enterprises seek digital technology on the shop floor and throughout production activities to intelligently connect life science manufacturing to the rest of the business and integrate advanced technologies like machine learning and IoT to help modernize manufacturing operations.
To view a copy of this recording, please click here.
Featured Speakers:
- Bart Reitter, VP Life Sciences (QAD)
- Greg Cathcart, CEO (Excellis Health Solutions
Date/Time: December 1 @ 1PM EST
Episode 3: Effective Enterprise Management: Real-time Analytics Across the Entire Business
For life science companies to better manage disruption and change, they need trustworthy yet flexible core processes and data, while also ensuring decision makers have access to real-time business and value chain insight. Effective Enterprise Management delivers real-time analytics across the entire business.
During the third episode, we will discuss what types of disruptions impact many life science organizations and the benefits Effective Enterprise Management capabilities provide to them.
To view a copy of the recording, please click here.
Featured Speakers:
- Bart Reitter, VP Life Sciences (QAD)
- Greg Cathcart, CEO (Excellis Health Solutions
Date/Time: November 17 @ 1PM EST
Episode Two: Integrated Supplier Management – Real-time visibility of supplier performance
In today’s disruptive business environment, life science organizations require the exchange of real-time information with supply trading partners to better respond to market volatility and changing customer demands. Integrated Supplier Management creates value for life science companies by improving supplier collaboration and supply chain visibility, allowing for faster response to changes in supply and demand.
In the second episode, we will discuss how Integrated Supplier Management addresses supply chain challenges, risks, and disruptors for life science companies.
To view a copy of this recording, please click here.
As part of our on-going webinars on Serialization 2.0 and what still has to be done before 2023, we are dedicating time to discuss the importance of a Level 3 (L3) Site Server being part of that journey. If you have or are considering a L3, don’t miss this interactive conversation!
Date/Time: November 5 @ 12PM EST
Featured Speakers
- Chris Howell (ThermoFisher)
- Alf Goebel (Advanco)
- Greg Cathcart, CEO (Excellis Health Solutions)
To view a copy of the recording, click here.
An agile ERP solution can greatly improve business outcomes for finance, supply chain, production, customer management, and other objectives. Too often, companies select big ERP providers rather than fully understanding what a life science ERP system really offers.
In the first episode, we will discuss what life science organizations need to consider when selecting enterprise systems, so they can meet the disruptions they face today and provide the flexibility needed to address tomorrow’s challenges.
Featured Speakers:
- Bart Reitter, VP Life Sciences (QAD)
- Greg Cathcart, CEO (Excellis Health Solutions
Date/Time: November 3 @ 1PM EST
To view a copy of this recording, click here.
Date/Time: October 15 @ 3PM EST
Guest Speaker: Chirag Shah, Director – Product & Supply Chain Security (Sanofi)
Topic: Security End-to-End: How to Build Brand Protection Safeguards into CMO/CPO/3PL and Other Supply Chain Partner Relationships
Chirag Shah joins us to talk about what brands should be proactively doing to address counterfeiting and illicit trade risks across their partner networks. With counterfeiting and other healthcare products on the rise and supply chain networks becoming more complex, it’s more important than ever to get all of your supply chain partners in lockstep with your brand protection and security expectations and requirements.
To view a copy of the recording, please click here.
