In this Post we will look in to the GxP. This is common term as part of the compliance if we are working in any Life sciences industry.
What is GxP?
GxP is a group of compliance that the particular industry should adopt as part of the industrial / audit compliance.
G- Stands for Good
x- is Kind of Variable.
P-stands for Practice
we will see in detail few of the X- which the life science industry adapts.
Good Manufacturing Practice:
This process details the manufacturing process and also the process that are followed to eliminate the Risk.The industry need to adopt/ publish the quality standards that it will be following.It also describes the minimum deviation. for more info
Good Laboratory Practice.
This process details and defines the quality system for the laboratory. This applies to non clinical studies.One of the core objectives is to ensure and promote the safety and reliablility of chemical in non-clinical and laboratory testing. ..read more
Good Documentation Practice:
This process defines the standards on which the documents are created,stored and retrieved in the complete life cycle of the process.It needs to have permanent traceable records.for more info
Good Clinical Practice.
This practice defines on the process defined to conduct the clinical trial on the human bodies.High standards are required for clinical protocol. Read more