This Guide has been developed by ISPE’s GAMP Community of Practice (CoP), a worldwide community of practitioners and subject matter experts who over25 years have been developing internationally accepted guidance on risk-based approaches to safeguard patient safety, product quality, and data integrity. This Guide has been produced with significant input and review from regulators worldwide, including key specialists from leading regulatory authorities (MHRA and WHO) working in this area.
The ISPE GAMP Guide: Records and Data Integrity is intended to be a complete and comprehensive single point of reference covering the requirements, expectations, and principles of pharmaceutical data integrity. Topics covered include regulatory focus areas, the data governance framework, the data life cycle, culture and human factors, and the application of quality risk management to data integrity. As such, it is of great interest to anyone with a responsibility for ensuring data integrity, including:
- Executives and managers
- Process and data owners and data stewards
- Technical system owners
- System developers, maintainers, and users
- Quality assurance and quality control
- Clinical, manufacturing, and laboratory personnel
- Validation and compliance specialists
- Suppliers of systems and services
- IT and engineering professionals
Readers will gain an invaluable insight into the pressing hot topic of pharmaceutical data integrity, gaining an in-depth understanding of the key requirements and principles, as well as learn about practical approaches and techniques to effectively address data integrity challenges. The ISPE GAMP Guide: Records and Data Integrity will assist regulated companies and their suppliers to achieve the high level of data integrity expected by regulatory authorities worldwide. Please visit http://www.ispe.org/gampguide/records-pharmaceutical-data-integrity to purchase the Guide.
ISPE also offers a new two-day training course using the Guide, A GAMP Approach to Data Integrity, Electronic Records and Signatures, and Operation GxP Computerized Systems (T50) in San Diego, California, US; Copenhagen, Denmark; Tampa, Florida, US; and Manchester, England, UK. This course provides the tools and techniques to implement proper controls for data to ensure the integrity and validity of the information throughout the data life cycle.
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