What is GLP in finance?
What is GLP in finance?
Microfinance industry witnessed 84 per cent year-on-year growth in aggregate gross loan portfolio (GLP) of microfinance institutions in second quarter of the financial year 2016-2017, says a report.
What is GLP and GMP?
“GMP” is Good Manufacturing Practices, and “GLP” is Good Laboratory Practices. Both the GMP and the GLP are regulations that are governed by the Food and Drug Administration (FDA). These regulations are imposed for ensuring the safety and integrity of drugs.
What does GLP stand for in education?
General Learning Program (GLP) Elementary Special Education Programs.
What are the principles of GLP?
The Principles of Good Laboratory Practice (GLP) are a managerial quality control system covering the organisational process and the conditions under which non-clinical health and environmental studies are planned, performed, monitored, recorded, reported and retained (or archived).
Why do we need GLP?
In the experimental (non-clinical) research arena, good laboratory practice or GLP is a quality system of management controls for research laboratories and organizations to ensure the uniformity, consistency, reliability, reproducibility, quality, and integrity of products in development for human or animal health ( …
Why is GLP important?
Good Laboratory Practice embodies different principles which are designed to ensure and promote consistency, quality, safety, reliability and integrity of chemicals during non-clinical and laboratory testing. Nevertheless, GLP isn’t limited to chemicals only.
What are SOPs in laboratory?
Standard operating procedures (SOPs) incorporating safety and health considerations must be developed and followed when laboratory work involves the use of hazardous chemicals, especially “particularly hazardous substances.” SOPs are written instructions that detail the steps to be performed during a given experimental …
Why should you practice safety in the laboratory?
By becoming familiar with the laboratory you’re working in and always following proper safety procedures, you can help to prevent or eliminate hazards. You will also know the proper steps to take in the unfortunate event that something does go wrong.
What is good laboratory practices PPT?
GLP is a formal regulation that was created by the FDA (United states food and drug administration) in 1978. 3. Definition of GLP • GLP embodies a set of principles that provides a frame work within which laboratory studies are planned performed, monitored, and archived and reported.
What is Good Laboratory Practices guidelines?
Good laboratory practice or GLP is a set of principles intended to assure the quality and integrity of non-clinical laboratory studies that are intended to support research or marketing permits for products regulated by government agencies.
What is GLP Slideshare?
Good Laboratory Practice • Good Laboratory Practice is a quality system concerned with the organizational process and the conditions under which a study is planned, performed, monitored, recorded, archived and reported.
What is OECD GLP?
The OECD Principles of Good Laboratory Practice (GLP) ensure the generation of high quality and reliable test data related to the safety of industrial chemical substances and preparations. The principles have been created in the context of harmonising testing procedures for the Mutual Acceptance of Data (MAD).
What is NABL accreditation Slideshare?
2. About NABL NABL is an autonomous society providing Accreditation (Recognition) of Technical competence of a testing, calibration, medical laboratory & Proficiency testing provider (PTP) & Reference Material Producer (RMP). NABL stands for National Accreditation Board For Testing And Calibration Laboratories.
How do I get NABL certified?
The CAB is required to apply on (www.nablwp.qci.org.in) in the prescribed application form (NABL 151 for testing laboratories, NABL 152 for calibration laboratories, NABL 153 for medical laboratories, NABL 180 for Proficiency Testing Providers (PTP), NABL 190 for Reference Material Producers (RMP), NABL 154 for …
What are the benefits of NABL accreditation?
Benefits of NABL for healthcare providers
- Superior competence in the process of calibration.
- Potential increase in business due to customer confidence and satisfaction.
- Recognition and greater reach of products in domestic & international markets.
- Saving of time and money from reduced retesting of products.
What is accreditation of laboratory?
Laboratory accreditation is a widely accepted process of evaluation of a laboratory’s quality, performance, reliability and efficiency. It is a means to promote and enforce better quality in laboratory testing and to ultimately reduce testing errors.
What is ISO laboratory accreditation?
The accreditation body is responsible for assessing the quality system and technical aspects of your system to determine your compliance to the requirements of ISO/IEC 17025. It is the accreditation body that ultimately decides whether or not a laboratory is complying with the standard.
How do you certify a lab?
Direct certification typically requires the laboratory to submit an application that would include the following: legal name of the laboratory; laboratory location information; laboratory personnel qualifications including education and experience, type of analysis and methodology for which they are seeking …
What are quality standards in a lab?
Quality standards are an integral part of the quality system. They are designed to help laboratories meet regulatory requirements, including local health regulations, and monitor laboratory functions, thereby ensuring laboratory safety and consistency of performance.
How can I improve my lab quality?
Here’s a 7 step guide to help you improve your lab efficiency without taking shortcuts that reduce quality.
- Human resources.
- Equipment optimisation.
- Upgrade from paper.
- Get advice from your peers.
- Workspace organisation.
- Enhance your stock control.
- Write everything down (in detail) – but not on paper!
- Comments.
How do you write a lab quality manual?
Goals and objectives of laboratory • Mission/vision statement • Scope of the quality manual–areas to which this QM applies; include a statement that quality is everyone’s responsibility • Description of how the manual will be maintained, reviewed and updated • Quality policy • State the purpose for the quality manual.
What is a quality manual?
The quality manual is a document that describes the quality management system of an organization (ISO 15189). Its purpose is to: • clearly communicate information • serve as a framework for meeting quality system requirements • convey managerial commitment to the quality system.
How do you write a quality manual?
What Should Be Included In A Quality Manual?
- Introduction & Scope.
- Quality Management Principles.
- References and Definitions.
- Context of the Organization.
- Leadership.
- Management System Planning.
- Support.
- Operation.
What are the QMS documents?
Elements and requirements of a QMS
- The organization’s quality policy and quality objectives.
- Quality manual.
- Procedures, instructions, and records.
- Data management.
- Internal processes.
- Customer satisfaction from product quality.
- Improvement opportunities.
- Quality analysis.