ISO certification Services

Introduction of ISO 22301:2019 The first edition of ISO 22301 was launched in May 2012. it had been the primary truly internationally accepted standard on business continuity, and it consists of requirements to implement a Business Continuity Management System consistent with ISO Annex SL. As such, it stood in line with its prominent predecessors like ISO 9001 and ISO/IEC 27001. What is good in ISO 22301-2019? Here may be a summary of current modifications and similarities as compared to the first version: The PDC model diagram was deleted, as diagrams are hard to standardize and typically cause endless discussions and interpretations. Clauses 4 to 10 cover the components of PDCA, as before. There are not any normative references during this document. The terms and definitions were updated to incorporate the ISO Online Browsing Platform and therefore the IEC Electropedia ; both are web-based information platforms. In clause 3 “Terms and Definitions” several terms were ...

What is GMP Certification? Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. The main risks are: unexpected contamination of products, causing damage to health or even death; incorrect labels on containers, which could mean that patients receive the wrong medicine; insufficient or too much active ingredient, resulting in ineffective treatment or adverse effects. GMP covers all aspects of production; from the starting materials, premises and equipment to the training and personal hygiene of staff. Detailed, written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process ...

What is HSE-MS? HSE-MS (Health Safety & Environment Management System) is set of Guideline developed for considering environmental protection, Occupational Health and Safety at work as important as providing quality products. Normally department focus on Quality and Products, but HSE specifies that Health and Safety management must be implied in organization, special for the Chemical Industry. Background of HSE:  HSE MS came into the picture after few serious incidences were occurred in chemical industry like  Bhopal disaster (India) (1984) and Seveso disaster (Italy) (1976)  due to failure of the Management System. Bhopal Disaster (India) 1984:  Bhopal Gas Tragedy was world's worst industrial disaster, a gas leak incident, which happen in heart of the India and killed approximately 3,787 to 19,000+ people which happen on 2–3 December 1984 at the Union Carbide India Limited (UCIL) pesticide plant in Bhopal, Madhya Pradesh, India. This loss can nei...

ANTI-BRIBERY MANAGEMENT SYSTEM LEAD AUDITOR TRAINING A well-managed organization is expected to have an agreement plan supported by right management systems to assist it in complying with its legal obligations and commitment to integrity. An anti-bribery policy is a component of an overall compliance policy. The anti-bribery policy and supporting management system helps an organization to let alone or moderate the costs, risks and damage of involvement in bribery, to promote trust and self-confidence in business dealings and to improve its reputation. This document reflects worldwide good practice and can be used in all jurisdictions. It is applicable to small, medium and large organizations in all sectors, including public, private and not-for-profit sectors. The bribery risks facing an organization vary according to factors such as the size of the organization, the locations and sectors in which the organization operates, and the nature, scale and complexity of the organization...

Course Description BCMS (Business Continuity Management System) 22301:2012 Lead Auditor Training is a 5-day instructor-lead course. The course is constructed around a case study and each activity is applied to the case study as we move through the course. There are more than 25 auditing activities as well as multi-media that provide practice applying and gain in an understanding of the requirements of ISO 22301 and BCMS auditing practices. Also included are small “quizzes” taken during the course after each section. The purpose of the quizzes is to help attendees measure what they know and what requires further study. What is Training Objectives? ISO 22301 refresh/review the structure & requirements of ISO 22301:2012.To enable delegates understand Key concepts in Business Continuity Management System auditing. To impart/enhance practical auditing skills to become internationally recognized certified Auditor/Lead Auditor. To enable the delegates to plan, conduct & m...

ISO 13485:2016 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. Such organizations can be involved in one or more stages of the life-cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities (e.g. technical support). ISO 13485:2016 can also be used by suppliers or external parties that provide product, including quality management system-related services to such organizations. Requirements of ISO 13485:2016 are applicable to organizations regardless of their size and regardless of their type except where explicitly stated. Wherever requirements are specified as applying to medical devices, the requirements apply equally to associated services as supplied by the organizatio...