According to the European GMP rules, written procedures for transfer activities and their documentation are required. For example, a Transfer SOP, a transfer plan and a report are now mandatory and will be checked during inspections.
As participant of the online GMP Training "Product Transfer", from 20-21 October 2020, you will receive electronic documents like a Transfer SOP and a template for a Transfer Plan. The documents can be downloaded and are in Word format and can immediately be used after adoption for your own projects.
Regulatory Guidance Documents like the WHO guideline on transfer of technology in pharmaceutical manufacturing are also part of the Guideline Manager. Copyright protected documents are included with their table of contents only. Due to copyright reasons, the document is not available for purchase and can only be downloaded by participants of the ECA Product Transfer course.