Concept of glp
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The document defines Good Laboratory Practice (GLP) and describes its key principles and objectives. GLP provides a framework for conducting non-clinical health and environmental safety studies to ensure reliability and reproducibility. The main elements of GLP include qualified personnel, adequate facilities and equipment, standard operating procedures, test and control article handling, and documentation and record keeping. GLP aims to assure accurate study results and promote international acceptance of safety tests.
Concept of glp
- 1. Concept of GLP Sivasankar. P P-2113
- 2. What is GLP • Definition GLP embodies a set of principles that provides a framework within which laboratory studies are planned performed, monitored, reported and archived. (Medicines and Healthcare products Regulatory Agency-UK) • GLP is a quality system concerned with oqganizational process and the conditions underwhich non clinical health and environmental safety studies are planned ,performe, monitored , recorded, archived and reported (OECD,1997) • It should not be confused with laboratory safety • it is a system for quality to ensure the uniformity, consistency, reliability, reproducibility • Applicable to non clinical studies
- 3. Objectives of GLP • Two standard 1. U.S (FDA regulated, 1978) 2.OECD (International standard,1981) Assurance of true result. GLP is to certify that every step of the analysis is valid or not. Assures data is traceable. Promotes international acceptance of tests.
- 5. Basic elements in GLP • Personnel Sponsor Management Study director Quality Assurance • Facility Laboratory Operation Animal care Equipment Reagents Storage 5 • Documents Protocols Standard Operating Reports Archiving • Test and control articles Characterization Handling Storage
- 6. 1. Personnel • In order to conduct GLP study Should have the Knowledge of the GLP principles. 1)There should be sufficient . 2)The personnel should be qualified. • Sponsor: person who initiates & supports nonclinical laboratory study, a person who submits nonclinical study to FDA or testing facility that initiates & conducts the study. • Facility management: Responsibilities of facility management is well defined. They designate a study director, as well as assure quality assurance unit is available, test and control articles are characterized
- 7. Contd… • Study director: He has overall responsibilities for technical conduct safety studies, as well as interpretation, analysis, documentation and reporting of results. • Quality Assurance unit: The quality assurance unit (QAU) serves an internal control function. It is responsible for monitoring each study to assure management that facilities, equipment, personnel, methods, practices, records, controls, SOPs, final reports (for data integrity), and archives are in conformance with the GLP
- 8. 2.Maintenance & Calibration of Equipment • Equipment shall be adequately inspected, cleaned & maintained • Equipment used for assessment of data shall be tested, calibrated and/or standardized • Scales & balances should be calibrated at regular intervals (usually ranging from 1-12 months)
- 9. 3.Reagent/ Materials Certification • This policy is to assure that reagents used are specified in the standard operating procedure. • Purchasing and testing should be handled by a quality assurance program. Requirements: • Reagents and solutions shall be labeled • Deteriorated or outdated reagents and solutions shall not be used • Include Date opened • Stored under ambient temperature
- 10. 4. Statistical Procedures for Data Evaluation • Statistical procedures are not simply chosen from a text book • Practitioners in a particular field may adopt certain standards • which are deemed acceptable within that field. • Regulatory agencies often describe acceptable statistical procedures.
- 11. 5. Test and control articles • Control articles or reference substances as they re-called in the OECD principles are of utmost importance as they are commonly used to calibrate the instrument. • Main requirements for control articles are: the identity, strength, purity, composition and other characteristics should be determined for each batch and documented. • The stability of each test and articles should also be determined. • Certified reference standards can be purchased from appropriate suppliers. If standards are not available , the recommendation is to take a lot of your own material and analyze, certify and use it as the standard.
- 12. 6.Analyst Certification • Some acceptable proof of satisfactory trainingand/or competence with specific laboratory procedures must be established for each analyst. • Qualification can come from education, experience or additional trainings, but it should be documented • Sufficient people • Requirements of certification vary
- 13. 7.Laboratory Certification • Normally done by an external agency • Evaluation is concerned with issues such as • Adequate space • Ventilation • Storage • Hygiene
- 14. 8.Standard operating procedures (SOP) • Written procedures for a laboratories program. • They define how to carry out protocol-specified activities. • Most often written in a chronological listing of action steps. • They are written to explain how the procedures are suppose to work • SOP • Routine inspection, cleaning, maintenance, testing and calibration. • Actions to be taken in response to equipment failure. • Analytical methods • Definition of raw data • Keeping records, reporting, storage, mixing, and retrieval of data
- 15. Contd… • Statistical procedures for data evaluation opinion from the expert it should be acceptable by the regulatory agency • Instrumentation validation • For any analytical laboratory the frequency for calibration, re-validation and testing depends on the instrument and extent of its use in the laboratory • Whenever an instrument’s performance is outside the “control limits” reports must be discontinued • Equipment records should include: Name of the equipment and manufacturer Model or type for identification Serial number Date equipment was received in the laboratory Copy of manufacturers operating instruction (s)
- 16. 8.Documentation and Maintenance of Records • Maintenance of all records provide documentation which may be required in the event of legal challenges due to repercussions of decisions based on the original analytical results. • General guidelines followed in regulated laboratories is to maintain records for at least five years • Length of time over which laboratory records should be maintained will vary with the situation
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