Download your free webinar summary to capture key insights into overcoming challenges such as:

Discover the critical importance “design for registration” or “manufacture for compliance” plays in optimizing global product launches.

Discover how you can maintain your focus on patient safety, market access, and commercial success with strategies for creating change management systems that facilitate regulatory intelligence sharing, cross-functional alignment, and efficiency.

Understand the function of UDI and access key takeaways on improving processes surrounding it, in your summary of a recent insight-packed webinar.

Capture valuable information on how your organization can better manage the complex and often conflicting regulatory environment you may be facing when designing your UDI systems and workflows.

Access the highlights and critical insights from “UDI Requirements: The Fear of the Unknown,” a recent webinar from Citeline’s MedTech Insight, presented in partnership with IQVIA Technologies. Discover how a comprehensive, single-source-of-truth UDI solution can support you in overcoming your country-specific operational challenges.

Download now for the answers to these questions, and more:

• What are the launch challenges facing MedTech today?
• What does a global launch entail?
• What are the considerations in launch strategy design?
• How can you design for local dependencies?
• How can you design transparent communication channels?
• How can global product lifecycles be enhanced with AI?
• What is an advanced solution for achieving global regulatory compliance?

As the use of AI becomes more widespread, drug and device developers are wondering how it can be leveraged to improve their processes. Pharma Ignite, in partnership with IQVIA Technologies, takes you inside the key considerations for using AI to augment and enhance QMS, with the aim of keeping developers in compliance and ensuring patient safety.

Learn more now about:

• The state of QMS today
• Necessary elements for an effective QMS
• How AI can be used to streamline time-consuming QM tasks
• Understanding what AI can – and cannot – do within a QMS
• The role of humans in AI augmented systems
• Overcoming the barriers to AI adoption to reap the rewards of improved quality operations

Download your free webinar summary to capture key insights into overcoming challenges such as:

Discover the critical importance “design for registration” or “manufacture for compliance” plays in optimizing global product launches.

Discover how you can maintain your focus on patient safety, market access, and commercial success with strategies for creating change management systems that facilitate regulatory intelligence sharing, cross-functional alignment, and efficiency.

Understand the function of UDI and access key takeaways on improving processes surrounding it, in your summary of a recent insight-packed webinar.

Capture valuable information on how your organization can better manage the complex and often conflicting regulatory environment you may be facing when designing your UDI systems and workflows.

Access the highlights and critical insights from “UDI Requirements: The Fear of the Unknown,” a recent webinar from Citeline’s MedTech Insight, presented in partnership with IQVIA Technologies. Discover how a comprehensive, single-source-of-truth UDI solution can support you in overcoming your country-specific operational challenges.