Finecert

JP Nagar, Bangalore, Karnataka

ISO 17025 is the main international standard for general necessities for the competency of testing and calibration laboratories. ISO/IEC 17025:2017 is the most recent version of ISO 17025, updated from 2005. In major countries, ISO/IEC 17025 is the standard most labs should hold certification in order to be deemed technically competent. There are several commonalities with the ISO 9001 standard, however ISO/IEC 17025 is more specific in needs for competency, and applies on to those organizations that turn out testing and calibration results and relies upon additional technical principles producing several advantages for laboratories. This international ISO 17025 standard is applicable to all or any laboratory no matter size or the extent of the scope of testing and calibration practices. Its utilized by laboratories to develop their management system for quality, body and technical operations.

Good manufacturing practice (GMP) is a thought that ensures the product is systematically made and controlled consistent with quality standards. Its designed to reduce the risks to the patient concerned in any pharmaceutical production. GMP constitutes the license to work in pharmaceutical production and is a core condition worldwide. However, rules and interpretations disagree from country to country and alter often. Therefore, having absolutely trained consultants at hand to assist with the implementation of those rules is extremely necessary. GMP covers all aspects of production; from the beginning materials, premises and instrumentality to the training and personal hygiene of employees. Detailed, written procedures are essential for every method that would have an effect on the standard of the finished product.

HACCP stands for Hazard Analysis and critical control points. A food safety management system based on the principles of HACCP is a systematic approach to identifying and dominant hazards, whether microbiological, chemical or physical, that might create a threat to the assembly of safe food in easy terms, it involves identifying what might fail during a food system and planning a way to stop it.There are seven core HACCP principles Hazard AnalysisCritical control PointsCritical LimitsCritical control point MonitoringCorrective ActionsVerificationRecord Keeping

Iso/iec 27001 is an information security standard, part of the iso/iec 27000 family of standards, of which the last version was published in 2013, with a few minor updates since then. It is published by the international organization for standardization (iso) and the international electrotechnical commission (iec) under the joint iso and iec subcommittee, iso/iec jtc 1/sc 27.Iso/iec 27001 specifies a management system that is intended to bring information security under management control and gives specific requirements. Organizations that meet the requirements may be certified by an accredited certification body following successful completion of an audit.Most organizations have a number of information security controls. However, without an information security management system (isms), controls tend to be somewhat disorganized and disjointed, having been implemented often as point solutions to specific situations or simply as a matter of convention. Security controls in operation typically address certain aspects of it or data security specifically; leaving non-it information assets (such as paperwork and proprietary knowledge) less protected on the whole. Moreover, business continuity planning and physical security may be managed quite independently of it or information security while human resources practices may make little reference to the need to define and assign information security roles and responsibilities throughout the organization.

ISO 13485 is an international standard that specifies the quality management system necessities for organizations committed medical devices at any stage of the product lifecycle. This is able to embrace the planning, development, production, storage, distribution, installation, service and technical support of the device. The ISO 13485:2016 revision is the third edition of the standard and supersedes the previous ISO 13485:2013. This latest revision of the standard contains substantial updates relating to risk-based quality processes, supplier management, and strict adherence to regulative necessities. This standard is also applied to parties that offer material, product or services to the organization and is applicable to organizations of all sizes massive and little. Additionally, any processes needed to get or maintain compliance with the ISO 13485:2016 standard thats not performed inside the organization, remain the responsibility of the organization and should be enclosed among the quality management system. The organization should monitor, management and guarantee correct maintenance of the external processes.

The Conformity European (CE) Mark is outlined as the European Unions (EU) obligatory conformity marking for regulation the products sold-out within the European Economic space (EEA) since 1985. The CE marking represents a manufacturers declaration that product go with the EUs New Approach Directives. These directives not solely apply to product within the EU however con jointly for product that are manufactured in or designed to be sold-out within the EEA. This makes the CE marking recognizable worldwide even to those unacquainted with the EEA.A CE Mark is a symbol that has to be mounted to several product before theyll be sold-out on the European market. The mark indicates that a product:Fulfills the necessities of relevant European product directivesMeets all the necessities of the relevant recognized European consonant performance and safety standardsIs suitable and cannot endanger lives or property

ISO 17025 is the main international standard for general necessities for the competency of testing and calibration laboratories. ISO/IEC 17025:2017 is the most recent version of ISO 17025, updated from 2005. In major countries, ISO/IEC 17025 is the standard most labs should hold certification in order to be deemed technically competent. There are several commonalities with the ISO 9001 standard, however ISO/IEC 17025 is more specific in needs for competency, and applies on to those organizations that turn out testing and calibration results and relies upon additional technical principles producing several advantages for laboratories. This international ISO 17025 standard is applicable to all or any laboratory no matter size or the extent of the scope of testing and calibration practices. Its utilized by laboratories to develop their management system for quality, body and technical operations.