Dublin, May 13, 2025 (GLOBE NEWSWIRE) -- The "Data Integrity and Document Management Training Course" training has been added to ResearchAndMarkets.com's offering.

This concise course covers the background to data integrity, why it is important and how its requirements affect both paper-based and computer-based systems.

Document management and data integrity are a key focus of regulatory inspections, with both EU and FDA inspectors increasingly observing violations during GxP inspections. It has become a critical issue in document governance and regulators expect staff working in GxP roles to have been trained in this important area.

Ensuring data integrity is an important component of the pharma industry's responsibility to guarantee the safety, efficacy, and quality of drugs. Violations relating to document management and data integrity have led to numerous regulatory actions, in- cluding warning letters and critical inspection findings. To address these concerns, the FDA, EMA, MHRA and the World Health Organization (WHO) have all recently published data integrity guidelines.

The programme will include discussion of the latest MHRA data integrity guide and EMA TMF guideline that should be considered by organisations involved in any aspect of the GxP pharmaceutical lifecycle (GCP, GMP, GLP and GvP). You will gain an understanding of the requirements for ensuring data integrity, review data integrity inspection findings, and get practical advice on defining and implementing an appropriate data governance process for compliance with data integrity requirements.

Benefits of attending:

• Understand the importance of data integrity and good document practice
• Ensure you are compliant with the new EU trial master file (TMF) guideline
• Be aware of key regulations and guidelines
• Discuss QMS considerations for data integrity and document management
• Review document management and data integrity inspections to facilitate regulatory compliance
• Consider the requirements for document management and data integrity governance to prevent data integrity breaches
• This course is part of the GxP (Good x Practice) training course collection, which feature a variety of topic areas to ensure you comply with the regulations and quality guidelines.

Certification:

• CPD: 6 hours for your records
• Certificate of completion

Who Should Attend:

• Clinical trials
• Manufacturing
• Quality assurance/quality control
• Compliance
• Pharmacovigilance

Key Topics Covered:

Principles of data integrity and good documentation practice

• What is data integrity?
• Why is data integrity important?
• ALCOA principles
• Good documentation practice including paper and electronic records

Data integrity regulations and guidelines

• MHRA/WHO/FDA/EMA/PICS/ICH GCP R2 data integrity guidelines
• Group review and discussion of some key regulated documents including the latest MHRA data integrity guide

Document management and data integrity inspection findings

• MHRA, EMA findings, EU non-compliance reports
• FDA findings
• Group discussion on inspection findings

QMS considerations for Data integrity and documentation

• What are the elements of QMS for data integrity?
• Risk management considerations
• Data governance
• Discussion of participants experience and best practice for QMS and data governance

Data integrity for computer systems

• Computer system validation considerations
• What is expected for compliance for GxP systems?

Discussion of document and data integrity issues

• Data integrity and digital signatures
• Certified copies/true copies
• Managing and preventing data integrity breaches

For more information about this training visit https://www.researchandmarkets.com/r/j4kk8p

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