REGULATORY REQUIREMENTS RADAR
Follow the regulations and understand the impact for your operation
Our regulatory requirements radar, updated on a quarterly basis, is the essential road map to your travels in the world of serialization and traceability. The Excellis Europe global Regulatory Requirements Radar provides a comprehensive and detailed map of all global serialization/traceability requirements. It also delivers the “So what?” by setting out our expert interpretation of the requirements and what they mean for pharma manufacturers.
Our Radar offers practical guidance on understanding the requirements in the wider context to enable our customers to prepare an effective readiness program that will address your immediate requirements and add long-term strategic value to your business.
Unlike other lists of requirements that are available, the Excellis Europe Requirements Radar focuses on the “So what?”, offering an expert interpretation of the requirements and what they mean for pharma manufacturers, leading into practical guidance on understanding the requirements in the wider context and preparing an effective manufacturer readiness program both to address the immediate requirements but also tackling this work strategically in the more long-term context.
The Excellis Europe Regulatory Radar focuses on serialisation and traceability requirements. The radar aims to provide a comprehensive, systematic overview of existing and anticipated regulatory requirements for coding of pharmaceutical products.
The radar also details the enablers/capabilities necessary to fulfill the requirements along with a view of the role of supply chain participants in the requirement and their obligations
As well as recording technical details of specific coding requirements, the Excellis Europe Radar provides early warning of new and emerging coding requirements in order to feed the regulatory monitoring and assessment processes of pharma supply chain participants.