Study directors appointed by testing facility managers for non-clinical laboratory studies can use this template to comply with the final report requirement of Good Laboratory Practice (GLP) regulations. Based on both FDA regulation and OECD principles, this template can be used to do the following:
- Note changes in and deviations from the study plan or protocol,
- Summarize, present, evaluate, and discuss the results of the study,
- Describe circumstances that may have affected the quality or integrity of the data,
- Identify the locations where the study plan or protocol, samples of test and reference items, specimens, raw data, and the final report are to be stored, and
- Add the GLP Compliance Statement and the Quality Assurance Statement.
With Mitti you can
Digitize any process, procedure or policy
Eliminate mistakes made by paper-based processes
Create and share professional reports instantly
Confirm accountability and compliance with a digital log
With Mitti you can
Digitize any process, procedure or policy
Eliminate mistakes made by paper-based processes
Create and share professional reports instantly
Confirm accountability and compliance with a digital log
About author
Mitti (by SafetyCulture) is the operations system for every site, shift and standard. Trusted by 80,000 organizations in 190 countries, Mitti publishes free checklists, SOP templates, audit checklists and toolbox talk topics that turn paper processes into a digital audit trail. Download one, put it to work on your next inspection or shift, and see why teams keep coming back for more.