Regulatory: what are good documentation practices?
Course
About course
This free interactive course provides a high-level overview of good documentation practices (GDP) for the pharmaceutical and medical device industry. GDP are the guidelines you must follow and includes all documents and records created and handled in each step of your process from incoming materials to distribution of final products.
In the regulatory world it’s important to remember – if it’s not documented, it didn’t happen.
Key learnings:
- Recognize the importance of GDP
- Describe requirements and standards, records, and types of documentation
- Identify requirements for signatures, corrections, and updates
- Recognize falsification of data and documentation
After diving into the details, you’ll hear from an expert on the topic as well as find links to supporting resources. If you come across unfamiliar terms, check out the glossary of some key regulatory terms, processes, acronyms, and their definitions.
You can access and complete each lesson individually, with the full course taking around 20 minutes to complete.
Certification
You will get an online certificate after the course completion. You can view and download it in a section My Courses. With Cytiva Certificates, portions of our programs have been split into online modules, so you can earn a high quality knowledge in interactive format.
