Introduction:

GLP Certification in Kenya is a concept known as "Good Laboratory Practice," or GLP, which suggests guidelines to be followed to guarantee the accuracy and reliability of non-clinical laboratory studies used to support research or marketing authorizations. GLP is a practice that only applies to non-clinical procedures and investigations, not to all clinical studies. The term "Good Laboratory Practice" (GLP) is most frequently related to the pharmaceutical business.

GLP Certification for Clinical Laboratories in Kenya: Its Importance

The phrase "GLP-compliant" is frequently used in the weighing and laboratory industries. You may be aware of what that entails. What does "Good Laboratory Practice," or GLP, actually mean? GLP, first presented in 1972, is a quality control system that laboratories and other businesses use to guarantee the integrity, uniformity, and reproducibility of non-clinical investigations and testing.

Good Clinical Practices and other laws are used in clinical lab investigations to ensure the participants' safety. GLP regulations are solely focused on quality control; they are not concerned with the technical or scientific content of the research or how valuable the investigations are. Please continue reading to find out what GLP is and how it relates to your lab balances and scales!

WHAT DOES GOES GLP MEAN?

The GLP's five central tenets are:

• Resources: The research employees' duties must be detailed, and their credentials and training must be verified. Additionally, equipment must be in good operating order and adhere to a certification, maintenance, and calibration program.

• Characterization: Gaining as much knowledge as possible about the resources employed in your study is essential.

• Rules: To ensure that the results are repeatable, each test should be carried out using protocols and established standard operating procedures.

• Results: The study's techniques and conditions must be reflected in the raw data, and the final report, which is typically given to authorities, must include a description of how the analysis was carried out as well as the data's scientific interpretation. For a few years, easily accessible archives of the original data must be kept.

• Quality Assurance: To help ensure compliance with GLP requirements, GLP mandates that an entire team of independent personnel is assigned to a study.

What advantages does GLP have?

• between the time a document is created and when it is stored or deleted, there is a clear flow of traceability through a thorough trial.

• Improved confidence in the accuracy and dependability of laboratory data

• improved ability to deliver accurate findings on the first try

• Through the GLP system, laboratory activities' total productivity is increased, and brand reputation is improved thanks to good laboratory management.

• Reduced requirement for redoing work Significant decrease in time spent looking into instances or operations that don't generate money.

In Kenya, how do you obtain GLP Certification?

Contact the best GLP Consultant in Kenya at contact@factocert.com or through www.Factocert.com so that consulting experts can give you a project plan that will work if you are having trouble putting this GLP Certification management system into practice or are unsure how to obtain GLP Certification in Kenya.

Conclusion:

Guaranteeing the integrity and quality of test findings related to non-clinical safety studies is one of the core goals of the Principles of Good Laboratory Practice (GLP).

A set of guidelines known as good laboratory practice, or GLP Certification in Kenya, is meant to guarantee the integrity and quality of non-clinical laboratory investigations used to support research or marketing authorizations for goods subject to GLP government regulation.