In a GMP environment, documentation needs to meet certain requirements to ensure product quality and product safety. If an instruction or record is poorly documented, then the manufacture or Quality Assurance/Control of a product can be negatively impacted, potentially reducing patient safety. This webinar will provide an overview of the principles and applications of Good Documentation Practice (GDP) as they apply to the pharmaceutical industry.
What Will You Learn
The webinar will go over the following topics:
- GMP Principles regarding documentation
- Types of Documents and Records
- General Requirements
- Recording Numbers
- Dealing With Attachments and Printouts
- Using Scanned Documents
- Electronic Records and Signatures
Who should attend?
This webinar is applicable to all personnel working within a GMP environment involved with GMP documentation e.g, Production, Quality, Regulatory and R&D.
|Basic Member:||$0.01||— Sold Out|
|Basic Member Group Tickets:||$0.01||— Sold Out|
|Student Ticket:||$0.01||— Sold Out|
|Pro Ticket:||$0.01||— Sold Out|