Good Laboratory Practices

GLP is a quality system concerned with the organizational process and the conditions under which non-clinical health and environmental safety studies are planned, performed, monitored, recorded, archived, and reported.

- OECD Principles

AREAS COVERED IN SESSION

• Concepts of the Good Laboratory Practice

• Principles of GLP

• Organization and Personnel

• Facilities and Environment

• Equipment and Reagents

• Test Systems

• Test and Reference Items

• Standard Operating Procedures (SOP’s)

• Performance of the Test

• Reporting of Results

• Storage and Retention of Records and Materials

• Quality Assurance Program

ABOUT THE SPEAKER

Engr. Aldwin Tagapan is an active assessment team leader/technical assessor for ISO/IEC 17025:2017, ISO 15189:2012, and ISO/IEC 17020:2012 standards of the Department of Trade and Industry Philippine Accreditation Bureau (DTI-PAB). He conducts training and workshops on Validation Test Methods, Quality Assurance, and Quality Control in Chemical Analyses, Measurement Uncertainty, ISO/IEC 17025:2017, and 2005, among many others. 

He also assists in the establishment, implementation, and maintenance of management systems for testing laboratories, medical laboratories, inspection bodies, companies, products and services, and even the company's own quality management system. 

Engr. Tagapan has in-depth experience in conducting sampling, inspection, and analyses of the different commodities ranging from food to non-food, water, air, environmental samples, energy materials, mining and mining products, pharmaceutical products, raw materials, and finished products.