Course description
Data Integrity: Overview and Documentation Completion, Review and Approval
Problems with data integrity continue to lead to vigorous regulatory actions. Such issues can be prevented with a thorough knowledge and understanding of the regulators’ requirements. This eLearning course is aimed at anyone working in the Pharmaceutical Industry and is designed to provide an overview of what is meant by data integrity, what needs to be considered during documentation completion, review and approval and how to keep your data complete, consistent and accurate throughout the data lifecycle.
Upcoming start dates
Outcome / Qualification etc.
The key learning objectives are to provide an understanding of:
- Key data integrity terms and definitions
- Good documentation practice in relation to data integrity
- Good documentation design to allow good documentation completion and the five main types of errors within records
- Review and approval of documents, including making corrections
- Audit trail review
- Document right first time metrics
By completing/passing this course, you will attain the certificate of Completion.
Why choose NSF International, Health Sciences
Trained over 1,300 delegates on our CQI and IRCA certified GMP PQS lead auditor training course
Provided expert health sciences training for over 30 years
More people have become ‘Qualified Persons’ in Europe through our training programme than any other training provider
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Reviews
Average rating 5
Excellent - very well presented, and the course material was superb
I registered this course after recommendation from a friend and it is definitely worth registering for. I like the in depth of Data integrity issue this course has gone with few...
Very good training for Data Integrity.