Documentation and Data Integrity course

From March 19, 2022 to April 2, 2022
9:00h – 11:00h (UTC-5)

  • 100% online training
  • Duration: 6h
  • Limited places
  • Available In-Company

Data Integrity Training with STE Engipharm

This course is designed to provide a clear view of what data integrity means and how to build a solid data processing system, since the GMP guidelines focus on documentation such as the modifications that have led to the respective WHO reports 32, 37 and 45.

We will provide the necessary tools to correctly apply the guidelines on Data Integrity recently published by WHO in Report 55. We will thus comply with GMP by having accurate data appropriately collected, so that when inspections are carried out in our laboratory, we can demonstrate that our data is correct and that the operators adjusted to the process.

The course is taught by Jordi Botet, an expert consultant in GMP with extensive experience working in companies in the pharmaceutical sector and author of the book “Calidad Total Farmacéutica” (Total Pharmaceutical Quality).

What are the objectives?

The objective of this training will be to provide clear guidelines for the correct documentation processing in the pharmaceutical industry.

With these tools you will be able to keep your data complete, consistent, and accurate throughout the production process.

Who can take this course?

  • Quality control managers
  • Operations and manufacturing managers
  • Qualification and validation managers
  • Engineering and automation staff

Fill in the following form and download the brochure and registration form.