Life Sciences companies face the challenge of producing the documentation required for validation of software in order to comply with regulatory expectations as prescribed by international regulatory agencies such as the US Food and Drug Administration (FDA), European Medicines Agency (EMA), UK Medicines and Healthcare products Regulatory Agency (MHRA) and others. The SAP S/4HANA Validation: A Streamlined Approach webinar will demonstrate how companies can meet regulatory requirements, shorten the overall time frame and reduce the burden on staff, while also ensuring ongoing compliance through the use of an SAP Validation Compliance Package.
Key learnings:
- Arbour Group Background/Expertise
- Regulatory Expectations
- Documentation Requirements
- Roles & Responsibilities
- Ongoing Maintenance
- SAP Validation Compliance Package Demo
