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Pharmaceutical leaders are under unprecedented pressure to expedite regulatory processes, including label management. Product labels undergo multiple changes, due to factors ranging from safety and efficacy concerns to label graphic changes within the supply chain, which is compounded by the fact that drugs marketed in multiple countries must continuously adhere to labeling and regulatory standards that are often completely different.

It’s never too early to start planning for the future, adopting labeling automation as part of a comprehensive digital transformation strategy today will inevitably help chart the course for long-term success when innovations like intelligent label management and authoring adoption explodes.

In this webinar participants will build a better understanding of:

    • A future state label management, authoring and assembly blueprint

    • Current and future technologies supporting smarter ways of working
    • Extending labeling beyond local label approval and into the supply chain
    • How outsourcing plays a role and the vendor selection process
    • Identifying pitfalls early on, and the value change management

Learn how to lead your organization through the next generation of global labeling challenges and realize greater levels quality, efficiency and automation that’s driven by technology and outsourcing.

Speakers:

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Julian Backhouse

Associate Director, Product Management

IQVIA Technologies

Julian Backhouse offers 30 years experience across Retail, Life Sciences and Consumer Packaged Goods verticals in technology and consulting roles. At IQVIA, Julian’s focus on Regulatory content management, label authoring, approval and artwork; leading our labeling initiative. He joined IQVIA in 2017 from Veeva Systems (Director, Vault Strategy EU) after 2 years with Zinc Ahead (ZincMAPS) and 6 years with Eastman Kodak (Design2Launch).

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Cham Williams

Associate Director, Business Systems

IQVIA Technologies

Cham Williams has more than 20 years experience in the Life Science industry working globally for pharmaceutical, consulting and solution companies. Now at IQVIA, Cham is bridging the technology and business worlds to help design products that help shape the next generation of RIM solutions. His expertise includes managing regulatory technology, business process optimization and systems planning and implementation. Prior to IQVIA, Cham was a principal consultant advising clients on regulatory strategy and process development. He started his career at GSK where he was part of a pioneering submissions team recognized for submitting electronic CRFs, which later led to the development of electronic NDAs.

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Kiran Chinnalla

Assoc. Director, Global Regulatory Affairs

IQVIA

Kiran Chinnalla is a seasoned regulatory professional with over 14 years of experience in strategic and operational labeling. In his role with IQVIA, he is responsible for handling global and regional labeling projects including: generating concise, accurate and well written labeling documents, strategic process consulting, regulatory labeling transformation and technology enablement. Kiran is a pharmacist by qualification with post -graduation in Pharmacology.

Hosted by

Maire Gerrard

Custom Content Writer

Informa Pharma Intelligence

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