Webinar Access

Available On-Demand

Webinar: Impact Analysis – the Beginning of your Content Automation Journey

Managing Regulatory Changes and Artwork Content in the Digital Age – Getting Value from your Unstructured Content

Key challenges to managing the impact of an ever-increasing volume of regulatory labelling and artwork changes include:

• Increasing levels of laborious non-value add tasks for regulatory professionals
• Lack of central access to historical and up to date impact knowledge
• Complexity of automatically establishing document and document content relationships for accurate insight and decision making
• Creating value from unstructured data
• Managing the rising costs of compliance
  

Key learning objectives you will learn during this session:

1. How the regulatory professional can reduce laborious and time-consuming content management tasks from their day
2. How you can quickly and accurately assess the impact of a regulatory change
3. How IA can automatically establish document and document content relationships
4. How you can release real value from your unstructured data

Benefits of digitising impact analysis:

• Automate laborious manual functions and touch-points involved in identifying artwork components for change and getting labelling updates transferred into artwork briefs
• Reduce artwork implementation delays and need to destroy stock/re-print
• Reduce risk and time in aligning disconnected versions of printed vs Health Authority (regulatory regime, body) approved artwork content
• Reduce of CAPAs related to artwork implementation
• Reduce in the quantity of projects allowing for easier tracking and management
• Streamlined Projects – allowing capacity for unplanned/last minute changes to be redirected to facilitate late stage, or just in-time printing
• Free up valuable resources in the regulatory department

Who should attend:

• Regulatory Affairs
• Digital Transformation
• Artwork & Packaging
• Supply Chain
• Quality
• Procurement
• Operations
• Project Management

Tune in now to learn how you can overcome and manage the challenges of constant change in the end-to-end labelling and artwork process.

Suzanne has over 25 years of experience in Quality and Operations Management and was involved in the development of PS 9000 which is a quality standard that was specifically created for the packaging supply chain of the pharmaceutical industry. Suzanne is a qualified IRCA auditor for a range of standards.

Sam Cole

Sam has responsibility for all client engagement across Perigord’s software division. Sam has oversight of all implementation projects, having developed processes that ensure efficient, yet compliant, delivery of validated systems into Perigord’s customer base. Sam has over 15 years in delivering artwork and labelling solutions into the Life Science sector.

Jim Chesterman

Jim Chesterman is a labelling professional with over 25 years of consulting and international project management experience in the Pharma, Medical Devices and Consumer sectors, focusing on labelling, artwork, business process, solution design and system implementation and integration.

Brian Cox is an experienced artwork management professional with over 20 years of experience. In his role, Brian works directly with leading pharmaceutical clients across many aspects of the artwork production process and fully understands the complexities clients face when assessing the impact of an safety change.