Consumer Products & Chemical
October 18-21, 2021 | Virtual
4 TRACKS | 4 DAYS
| 1000+ ATTENDEES
There is no cost to attend this event.
Join your quality, regulatory, legal, marketing, and IT peers from the consumer goods, food and beverage, cosmetics, speciality chemical, and crop science industries at this virtual event designed especially for you.
Opening
Keynotes
October 18
Quality & HSE Management
October 19
Regulatory Compliance
October 20
Advertising Claims Management
October 21
CONNECT ROUNDTABLES
October 18 - 21
Connect Sessions2:00 PM CET / 8:00 AM ET / 5:00 AM PT
Roundtables, 1:1 Meetings, Networking
Opening Keynote3:00 PM CET / 9:00 AM ET / 6:00 AM PT
Chasing Product Compliance In A Consumer Oriented World
In the proliferating world of consumer preference, consumers are demanding full transparency across the value chain from raw material extraction through customer enjoyment to disposal. How impactful can this reframing be? Our keynote speakers will share real world examples of how companies are reframing product compliance to focus on the consumer.
Speakers
Enterprise Keynote4:15 PM CET / 10:15 AM ET / 7:15 AM PT
IT is from Mars, Business is from Venus
Product compliance transformation is a business imperative to accelerate innovation, reduce risk and lower costs. To succeed, IT and Business need deep mutual empathy and collaboration. Hear insights and learnings from our panel of IT and Business leaders on how to achieve the IT-Business mind-meld.
Speakers
Connect Sessions5:00 PM CET / 11:00 AM ET / 8:00 AM PT
Roundtables, 1:1 Meetings, Networking
Technology Keynote5:30 PM CET / 11:30 AM ET / 8:30 AM PT
Around The Corner
Veeva's product leadership will review key challenges facing regulated industries like consumer goods, chemicals, and cosmetics and how Veeva's product roadmaps will address these challenges across quality, regulatory, and product claims management.
Speakers
Customer Keynote6:15PM CET / 12:15 PM ET / 9:15 AM PT
A Master Class in Supplier Collaboration
Unilever sits down for a fireside "master class" in supplier collaboration. This session will explore how Unilever has consistently achieved top analyst rankings for achievement in supplier agility, digital transformation, and sustainability, and what Unilever is focused on next.
Speakers
Connect Sessions7:00 PM CET / 1:00 PM ET / 10:00 AM PT
Roundtables, 1:1 Meetings, Networking
Connect Sessions2:00 PM CET / 8:00 AM ET / 5:00 AM PT
Roundtables, 1:1 Meetings, Networking
Keynote3:00 PM / CET 9:00 AM ET / 6:00 AM PT
How AI and Automation Can Support Product Compliance Across Your Supply Chain
AI and machine learning are not just buzzwords. Hear how Veeva customers are incorporating automation and AI into their Quality strategy while steering clear of false promises. Particpants in this session will see how agility and compliance are brought together in your supplier interactions.
Speakers
Concurrent4:00 PM CET / 10:00 AM ET / 7:00 AM PT
Modernizing Food Safety and Quality: from Product Innovation to Manufacturing
The past year has highlighted the value of modernizing quality processes while dealing with increased food safety and supply chain regulatory requirements. The need to quickly adapt and respond to increasing challenges has compelled organizations to evaluate their reliance on legacy technology and take action. In fact, a recent survey of global quality leaders found that 42% plan to upgrade to a global eQMS in 2021. In this session participants will learn from industry experts on how they can modernize food safety and quality and critical items to consider from product innovation to retail.
Speakers
How to Avoid Common QHSE Risk Management Pitfalls
The majority of companies today have experienced a severe QHSE event, which often reveal important gaps in the way the company operates. Whether it was a serious employee accident, an accidental release of toxic gas in a populated area, a delivery of damaged or contaminated products on a large number of consumers, these types of incidents remind us how crucial it is for a company, regardless of its size, to develop a culture of anticipation and risk management. How can companies properly manage QHSE risks? What mistakes can be avoided, or best practices to adopt? Join this session to hear insights from experienced field managers from different regulated industries on this topic.
Speakers
Connect Sessions5:00 PM CET / 11:00 AM ET / 8:00 AM PT
Roundtables, 1:1 Meetings, Networking
Product Roadmap6:00 PM CET / 12:00 PM ET / 9:00 AM PT
Veeva QualityOne
Veeva's quality strategy and product experts will share our vision and plans relevant to quality & HSE professionals. You won't want to miss this glimpse into what we have in store for our valued customers.
Connect Sessions7:00 PM CET / 1:00 PM ET / 10:00 AM PT
Roundtables, 1:1 Meetings, Networking
Connect Sessions2:00 PM CET / 8:00 AM ET / 5:00 AM PT
Roundtables, 1:1 Meetings, Networking
Keynote3:00 PM CET / 9:00 AM ET / 6:00 AM PT
Eating an Elephant – Demystifying the Digital Product Compliance Journey
Advancements in digital technology are prompting chemical & consumer goods companies to reimagine the way they do business. Yet product stewardship and regulatory groups in these organizations are often the last to find out about digital transformation. In this session you will hear from industry leaders and learn how to launch the digital product compliance journey in your organization through a logical step-by-step approach.
Speakers
Fireside Chat4:00 PM CET / 10:00 AM ET / 7:00 AM PT
Competitive Compliance: The Transformation from Cost Center to Top Line Business Driver
The ability to meet growing regulator and societal demands for high-quality, safe, sustainable, and compliant products is a strategic imperative. However the product compliance function is still often viewed as an obligatory cost of doing business, versus an opportunity to drive revenue, reduce costs, and build customer trust. In this session you will hear how one organization unlocked significant value by transforming to a more customer-centric product compliance operating model.
Speakers
Connect Sessions5:00 PM CET / 11:00 AM ET / 8:00 AM PT
Roundtables, 1:1 Meetings, Networking
Speak Your CEOs’ Language6:00 PM CET / 12:00 PM ET / 9:00 AM PT
Speak Your CEOs’ Language: How to Build the Business Case for Compliance Transformation
Transforming product compliance delivers a range of benefits from greater operational efficiency to the ability to grow customer trust and drive topline growth. Yet compliance teams often struggle to articulate to executives what product compliance transformation is worth and how it will generate concrete business value. Join this session to learn how to build a competitive business case that ensures your digital product compliance project is funded and earns a seat at the strategy table.
Speakers
Connect Sessions7:00 PM CET / 1:00 PM ET / 10:00 AM PT
Roundtables, 1:1 Meetings, Networking
Connect Sessions2:00 PM CET / 8:00 AM ET / 5:00 AM PT
Roundtables, 1:1 Meetings, Networking
Panel3:00 PM CET / 9:00 AM ET / 6:00 AM PT
Advertising Claims Management as a Driver of Speed, Growth and Innovation
Think advertising claims management is all about compliance and risk avoidance? Think again. As rapidly as consumer tastes change or markets shift, forward thinking companies need to assert compelling claims to exploit brief windows of opportunity. How can companies expect to delight consumers under such tight timelines? Hear from industry veterans about how they are thinking about advertising claims as a driver of speed, growth and innovation.
Speakers
Panel4:00 PM CET / 10:00 AM ET / 7:00 AM PT
Managing Advertising Claims in a Digital and Social World
The rise of digital advertising, in particular of social media and influencers, has made the process of managing and tracking claim approvals and usage exponentially more difficult. Marketers must seize brief windows of opportunity to stay timely and relevant, which makes a traditional, formal approval process self defeating. Furthermore, influencers, whether paid or unpaid often have their own ideas about the products they use and seldom keep to a script. How are companies, regulators and advertising platforms adjusting to this new claims landscape, and what does the future look like for claims in a digital world?
Speakers
Connect Sessions5:00 PM CET / 11:00 AM ET / 8:00 AM PT
Roundtables, 1:1 Meetings, Networking
Panel6:00 PM CET / 12:00 PM ET / 9:00 AM PT
Key Learnings Across Veeva Claims Implementations
Advertising claims management is a very complex process. As Veeva has implemented with customers across geographies, categories, and sizes, there are some striking similarities, and some marked differences. Join John Cooper, Director of Strategy for Veeva Claims, and Chris Veale, Global Practice Manager for Claims Implementations, as they discuss some of the more interesting commonalities and differences. Special guest, Narisa Bandali, Staff Attorney from BISSELL Homecare, will provide a customer perspective.
Speaker
Connect Sessions7:00 PM CET / 1:00 PM ET / 10:00 AM PT
Roundtables, 1:1 Meetings, Networking
ROUNDTABLE CONNECT
PRODUCT DEMONSTRATIONS
October 18
Digital Trends in Quality and Regulatory2:00 - 2:45 PM CET / 8:00 - 8:45 AM ET / 5:00 - 5:45 AM PT
Join the Veeva strategy team to discuss key themes from recent Quality and Regulatory Practitioner surveys.
Managing Complaints with Vault - CRM Integration Use Case5:00 - 5:25 PM CET / 11:00 - 11:25 AM ET / 8:00 - 8:25 AM PT
Join this session to see how Veeva applications can talk to other apps. In this example you will see how a Case originating in Salesforce CRM can be sent to QualityOne for Complaint follow up and investigation.
Unify Master Data with Compliance5:00 - 5:25 PM CET / 11:00 - 11:25 AM ET / 8:00 - 8:25 AM PT
Compliance teams need master data but find such systems lack flexibility and usability. See how your master data and compliance data can be unified in a holistic, connected compliance tool that enables product transparency.
7 Tips for Streamlining Your Procurement Process5:00 - 5:25 PM CET / 11:00 - 11:25 AM ET / 8:00 - 8:25 AM PT
In this session we will share seven tips that you can use immediately to streamline your procurement process, increase efficiency for both parties, and eliminate roadblocks that often bog down the procurement process.
Digital Trends in Quality and Regulatory7:00 - 7:45 PM CET / 1:00 - 1:45 PM ET / 10:00 - 10:45 AM PT
Join the Veeva strategy team to discuss key themes from recent Quality and Regulatory Practitioner surveys.
October 19
Best Practices for Change Management2:00 - 2:45 PM CET / 8:00 - 8:45 AM ET / 5:00 - 5:45 AM PT
Join this session to understand best practices to migrate new configuration, refresh your vault and keep all your environments in sync.
Best Practices: QualityOne Reports and Dashboards2:30 - 2:55 PM CET / 8:30 - 8:55 AM ET / 5:30 - 5:55 AM PT
Join this demonstration showing how to use the recently introduced report features to provide you with the data you need.
Best Practices for Change Management5:00 - 5:25 PM CET / 11:00 - 11:25 AM ET / 8:00 - 8:25 AM PT
Join this session to understand best practices to migrate new configuration, refresh your vault and keep all your environments in sync.
A Case Study in eQMS5:00 - 5:25 PM CET / 11:00 - 11:25 AM ET / 8:00 - 8:25 AM PT
The expanding legalization and applications for CBD brings greater oversight and compliance. Our panelists will discuss how Veeva's eQMS software provides not only a critical foundation for compliance but also competitive advantage in a rapidly evolving industry.
Best Practices: QualityOne Reports and Dashboards5:30 - 5:55 PM CET / 11:30 - 11:55 AM ET / 8:30 - 8:55 AM PT
Join this demonstration showing how to use the recently introduced report features to provide you with the data you need.
October 20
Best Practices: RegulatoryOne Reports and Dashboards2:00 - 2:25 PM CET / 8:00 - 8:25 AM ET / 5:00 - 5:25 AM PT
Join this demonstration showing how to use the recently introduced report features to provide you with the data you need.
Implementation Success Best Practices2:30 - 2:55 PM CET / 8:30 - 8:55 AM ET / 5:30 - 5:55 AM PT
Best Practices: RegulatoryOne Reports and Dashboards7:30 - 8:00 PM CET / 1:30 - 2:00 PM ET / 10:30 - 11:00 AM PT
Assess your registrations demands, identify and check market specific requirements.
Implementation Success Best Practices7:30 - 8:00 PM CET / 1:30 - 2:00 PM ET / 10:30 - 11:00 AM PT
October 21
Ask Me Anything about Claims2:20 - 3:00 PM CET / 8:20 - 9:00 AM ET / 5:20 - 6:00 AM PT
In this session, Veeva Claims experts will sit in the hot seat, answering the most frequently asked questions about managing product and advertising claims in an integrated system.
Ask Me Anything about Claims7:20 - 8:00 PM CET / 1:20 - 2:00 PM ET / 10:20 - 11:00 AM PT
In this session, Veeva Claims experts will sit in the hot seat, answering the most frequently asked questions about managing product and advertising claims in an integrated system.
October 19
Demonstration: QualityOne HACCP2:00 - 2:25 PM CET / 8:00 - 8:25 AM ET / 5:00 - 5:25 AM PT
Replace your spreadsheets by easily creating and managing HACCP plans on a single platform with automated workflows and task management that are built to scale on a flexible and configurable platform. Leverage existing HACCP studies to increase efficiency and gain insight by drawing information from a Hazard library and linking to product & ingredient information records
Increase visibility and transparency across your organization by reporting on detailed information within individual HACCP plans and creating dashboards to highlight trends across multiple HACCP plans.
Veeva’s HACCP solution is developed based on Codex Alimentarius principles, and is compliant with GFSI benchmark requirements.
Demonstration: QualityOne Documents & Training Management2:00 - 2:25 PM CET / 8:00 - 8:25 AM ET / 5:00 - 5:25 AM PT
Document Management is an essential part of compliance requirements in regulated industries subject to GxP and ISO standards. Everyone works from one single source of truth - the most current (and approved) document. While version control gives you a clear audit trail for information. The Document Management dashboard allows you to track and monitor document status to improve review cycle times.
Seamlessly assign, manage, track training tasks using flexible, role-based alignment of users and related content. Learners can easily view upcoming or complete training tasks on any device - even outside the office. Demonstrate compliance with centralized training records and configurable reports that ensure you're always audit-ready.
Demonstration: QualityOne HSE Incident Management2:00 - 2:25 PM CET / 8:00 - 8:25 AM ET / 5:00 - 5:25 AM PT
QualityOne's HSE Incident Management capabilities are critical to ensuring compliance to local and international regulations and standards. With QualityOne users can quickly and easily capture and investigate HSE events including injuries, illnesses, property and vehicle damages, near misses, hazards and environmental releases. They can also assess incident criticality or risk level and resolve to prevent future occurrences, and investigate and identify root causes using built-in 5 Whys Methodology.
QualityOne's HSE incident management capabilities allow users to create, assign, and track corrective and preventive actions to completion, including training assignment actions. They can also report incidents from anywhere on any device with the QualityOne HSE Incident Management mobile app. Using QualityOne's built-in reporting and dashboard functionality, monitor all your HSE KPIs in real-time and identify trends.
Demonstration: QualityOne Inspections & CoA Automation2:30 - 2:55 PM CET / 8:30 - 8:55 AM ET / 5:30 - 5:55 AM PT
With QualityOne's inspection management capabilities, users can easily create inspection records and analyze samples against predefined inspection plans and evaluation criteria where critical to quality parameters are defined. The system will automatically determine if sample or material is acceptable or not by comparing test results entered to the parameters on the specification. Save time and money with Veeva’s Certificate of Analysis (CoA) inspection capabilities provide you the ability to automatically analyze CoA files. The CoA solution uses an automated process to determine if the measurement values on the CoA meet specification limits. Increase compliance and supplier collaboration by easily bringing your suppliers securely into the process and having them directly input the required data.
Demonstration: QualityOne Mobile2:30 - 2:55 PM CET / 8:30 - 8:55 AM ET / 5:30 - 5:55 AM PT
eQMS software also offers users the ability to utilize software from mobile devices such as smartphones and tablets. This enhances user efficiency, as mobile readiness allows data quality to be easily managed and maintained from anywhere, and at any time.
Changes like this can entirely shift the way your organization approaches quality management. You don’t need to wait for your entire team to be sitting together in one office panning through data. Rather, everyone on the team can make small efforts and conduct analysis whenever they have time and wherever they are. New insights can be more easily found, and meetings about quality become shorter and more focused.
Demonstration: QualityOne HACCP5:00 - 5:25 PM CET / 11:00 - 11:25 AM ET / 8:00 - 8:25 AM PT
Replace your spreadsheets by easily creating and managing HACCP plans on a single platform with automated workflows and task management that are built to scale on a flexible and configurable platform. Leverage existing HACCP studies to increase efficiency and gain insight by drawing information from a Hazard library and linking to product & ingredient information records.
Increase visibility and transparency across your organization by reporting on detailed information within individual HACCP plans and creating dashboards to highlight trends across multiple HACCP plans.
Veeva’s HACCP solution is developed based on Codex Alimentarius principles, and is compliant with GFSI benchmark requirements.
Demonstration: QualityOne Documents & Training Management5:00 - 5:25 PM CET / 11:00 - 11:25 AM ET / 8:00 - 8:25 AM PT
Document Management is an essential part of compliance requirements in regulated industries subject to GxP and ISO standards. Everyone works from one single source of truth - the most current (and approved) document. While version control gives you a clear audit trail for information. The Document Management dashboard allows you to track and monitor document status to improve review cycle times.
Seamlessly assign, manage, track training tasks using flexible, role-based alignment of users and related content. Learners can easily view upcoming or complete training tasks on any device - even outside the office. Demonstrate compliance with centralized training records and configurable reports that ensure you're always audit-ready.
Demonstration: QualityOne HSE Incident Management5:00 - 5:25 PM CET / 11:00 - 11:25 AM ET / 8:00 - 8:25 AM PT
QualityOne's HSE Incident Management capabilities are critical to ensuring compliance to local and international regulations and standards. With QualityOne users can quickly and easily capture and investigate HSE events including injuries, illnesses, property and vehicle damages, near misses, hazards and environmental releases. They can also assess incident criticality or risk level and resolve to prevent future occurrences, and investigate and identify root causes using built-in 5 Whys Methodology.
QualityOne's HSE incident management capabilities allow users to create, assign, and track corrective and preventive actions to completion, including training assignment actions. They can also report incidents from anywhere on any device with the QualityOne HSE Incident Management mobile app. Using QualityOne's built-in reporting and dashboard functionality, monitor all your HSE KPIs in real-time and identify trends.
Demonstration: QualityOne Inspections & CoA Automation5:30 - 5:55 PM CET / 11:30 - 11:55 AM ET / 8:30 - 8:55 AM PT
With QualityOne's inspection management capabilities, users can easily create inspection records and analyze samples against predefined inspection plans and evaluation criteria where critical to quality parameters are defined. The system will automatically determine if sample or material is acceptable or not by comparing test results entered to the parameters on the specification. Save time and money with Veeva’s Certificate of Analysis (CoA) inspection capabilities provide you the ability to automatically analyze CoA files. The CoA solution uses an automated process to determine if the measurement values on the CoA meet specification limits. Increase compliance and supplier collaboration by easily bringing your suppliers securely into the process and having them directly input the required data.
Demonstration: QualityOne Mobile5:30 - 5:55 PM CET / 11:30 - 11:55 AM ET / 8:30 - 8:55 AM PT
eQMS software also offers users the ability to utilize software from mobile devices such as smartphones and tablets. This enhances user efficiency, as mobile readiness allows data quality to be easily managed and maintained from anywhere, and at any time.
Changes like this can entirely shift the way your organization approaches quality management. You don’t need to wait for your entire team to be sitting together in one office panning through data. Rather, everyone on the team can make small efforts and conduct analysis whenever they have time and wherever they are. New insights can be more easily found, and meetings about quality become shorter and more focused.
Demonstration: QualityOne QMS7:00 - 7:25 PM CET / 1:00 - 1:25 PM ET / 10:00 - 10:25 AM PT
Veeva Quality Management Software (eQMS) gives your suppliers and contract manufacturers full (and secure) access to business critical quality control documents and the ability to directly participate in quality processes.
You’ll have 100% visibility, accountability and tracking across supplier certifications, supplier audits, SCARs, and supplier performance.
Demonstration: QualityOne Documents & Training Management7:00 - 7:25 PM CET / 1:00 - 1:25 PM ET / 10:00 - 10:25 AM PT
Document Management is an essential part of compliance requirements in regulated industries subject to GxP and ISO standards. Everyone works from one single source of truth - the most current (and approved) document. While version control gives you a clear audit trail for information. The Document Management dashboard allows you to track and monitor document status to improve review cycle times.
Seamlessly assign, manage, track training tasks using flexible, role-based alignment of users and related content. Learners can easily view upcoming or complete training tasks on any device - even outside the office. Demonstrate compliance with centralized training records and configurable reports that ensure you're always audit-ready.
October 20
Demonstration: RegulatoryOne - Regulatory Document Management2:00 - 2:25 PM CET / 8:00 - 8:25 AM ET / 5:00 - 5:25 AM PT
Increase regulatory collaboration, transparency & traceability with one single point of truth for regulatory documents.
Demonstration: RegulatoryOne - Regulatory Requests2:00 - 2:25 PM CET / 8:00 - 8:25 AM ET / 5:00 - 5:25 AM PT
Respond to customers & authorities with speed and accuracy as well as get transparency and consistency in your communication streams.
Demonstration: RegulatoryOne - Registrations Dossiers Management2:30 - 2:55 PM CET / 8:30 - 8:55 AM ET / 5:30 - 5:55 AM PT
Assess your registrations demands, identify and check market specific requirements.
Demonstration: RegulatoryOne - Compliance Management2:30 - 2:55 PM CET / 8:30 - 8:55 AM ET / 5:30 - 5:55 AM PT
Create transparency and accelerate compliance checks for formulation compositions.
Product Roadmap: RegulatoryOne5:00 - 5:45 PM CET / 11:00 - 11:45 AM ET / 8:00 - 8:45 AM PT
Demonstration: RegulatoryOne - Regulatory Document Management7:00 - 7:25 PM CET / 1:00 - 1:25 PM ET / 10:00 - 10:25 AM PT
Increase regulatory collaboration, transparency & traceability with one single point of truth for regulatory documents.
Demonstration: RegulatoryOne - Compliance Management7:00 - 7:25 PM CET / 1:00 - 1:25 PM ET / 10:00 - 10:25 AM PT
Create transparency and accelerate compliance checks for formulation compositions.
Demonstration: RegulatoryOne - Regulatory Requests7:30 - 8:00 PM CET / 1:30 - 2:00 PM ET / 10:30 - 11:00 AM PT
Respond to customers & authorities with speed and accuracy as well as get transparency and consistency in your communication streams.
Demonstration: RegulatoryOne - Registrations Dossiers Management7:30 - 8:00 PM CET / 1:30 - 2:00 PM ET / 10:30 - 11:00 AM PT
Assess your registrations demands, identify and check market specific requirements.
October 21
Demonstration: Veeva Claims - Using the Claims Library2:00 - 2:20 PM CET / 8:00 - 8:20 AM ET / 5:00 - 5:20 AM PT
This session shows what it's like to have a central claims library instead of documents and excel spreadsheets. It shows the fundamental functionality of Veeva Claims using the capabilities of the vault platform like searching, filtering, understanding local adaptations and substantiations.
Demonstration: Veeva Claims - Marketing Material Review and Approval2:20 - 2:40 PM CET / 8:20 - 8:40 AM ET / 5:20 - 5:40 AM PT
Most of our Veeva Claims customers are using the claims functionality, but only some are connecting the downstream marketing materials to Claims. This session show how a marketer could request social media assets, and how those can be reviewed and approved in connection with the claims they possess.
Demonstration: Veeva Claims - Challenge Response2:40 - 3:00 PM CET / 8:40 - 9:00 AM ET / 5:40 - 6:00 AM PT
When a claim is challenged it can day days or weeks to assemble documentation and summary data, unless it's already in a library with meaningful relationships. This session shows how easy it can be to respond to a claim challenge with Veeva Claims.
Demonstration: Veeva Claims - Localizing Packaging Copy5:00 - 5:20 PM CET / 11:00 - 11:20 AM ET / 8:00 - 8:20 AM PT
Veeva Claims has new functionality for localizing packaging elements which can reduce errors in local packaging and save time. Join this session to learn more and dive deeper into the pack copy capabilities of Veeva Claims.
Product Roadmap: Veeva Claims5:20 - 6:00 PM CET / 11:20 - 12:00 PM ET / 8:20 - 9:00 AM PT
Demonstration: Veeva Claims - Using the Claims Library7:00 - 7:20 PM CET / 1:00 - 1:20 PM ET / 10:00 - 10:20 AM PT
This session shows what it's like to have a central claims library instead of documents and excel spreadsheets. It shows the fundamental functionality of Veeva Claims using the capabilities of the vault platform like searching, filtering, understanding local adaptations and substantiations.
Demonstration: Veeva Claims - Marketing Material Review and Approval7:20 - 7:40 PM CET / 1:20 - 1:40 PM ET / 10:20 - 10:40 AM PT
Most of our Veeva Claims customers are using the claims functionality, but only some are connecting the downstream marketing materials to Claims. This session show how a marketer could request social media assets, and how those can be reviewed and approved in connection with the claims they possess.
Demonstration: Veeva Claims - Challenge Response7:40 - 8:00 PM CET / 1:40 - 2:00 PM ET / 10:40 - 11:00 AM PT
When a claim is challenged it can day days or weeks to assemble documentation and summary data, unless it's already in a library with meaningful relationships. This session shows how easy it can be to respond to a claim challenge with Veeva Claims.
There is no cost to attend this event.
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