IMPLEMENTATION TRAINING What is Implementation Training? This course is designed to assist candidates to implement a process-based quality system in accordance with the standard. Learning outcome: Understand the origin of quality and particularly, the ISO series of the standards. I Understand how the clauses of the standard carpet are implemented in an effective and user-friendly […]
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INTERNAL AUDIT TRAINING What is Internal Audit Training? The internal auditing of your quality management system course is designed to prepare you to schedule, plan and conduct ISO internal auditing in compliance with the requirement of standards. This fast paced course includes case studies and exercises to help you fully understand auditing process. We cover
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LEAD AUDITOR TRAINING What is Lead Auditor Training? A five-day course provides training to ensure that the participant thoroughly understand the role and acquires the expertise in effectively establishing, implementing, maintaining and Auditing Management system. At the end of the course the participant will be able to: • Understand the purpose of standards and their
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ANSI/ESD S20.20 AND IEC61340-5-1 ESD What is ANSI/ESD S20.20 AND IEC61340-5-1 ESD? China has become the most important electronic product production base in the world. However, when it comes to on-site audits, many enterprises are often rejected due to electrostatic discharge management problems, which causes faults in electronic products after they reach the market. ANSI/ESD
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GDP CERTIFICATION – GOOD DISTRIBUTION PRACTICES What is GDP? Good Distribution Practices (GDP) is a quality system for warehouses and distribution centers dedicated to medicines. Internationally accepted pharmaceutical GDP regulations stipulate that distributors of pharmaceutical products must align their operations with the standards. The scheme ensures that consistent quality management systems are in place throughout
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WHO GMP CERTIFICATION What is WHO GMP? Good Manufacturing Practices (GMP, also referred to as ‘cGMP‘ or ‘current Good Manufacturing Practice‘) is the aspect of quality assurance that ensures that medicinal products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the product specification. GMP defines
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GLP CERTIFICATE – GOOD LABORATORY PRACTICES What is 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 (including pharmaceuticals) through non-clinical safety tests; from physiochemical properties through acute to
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GMP CERTIFICATION – GOOD MANUFACTURING PRACTICES What is GMP? GMP stands for Good Manufacturing Practice, & the term is used globally for managing the control and management of manufacturing, testing, and overall quality of pharmaceutical products. It defines certain guidelines that talk about the quality assurance approach. GMP certification ensures that products are produced following
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HACCP – HAZARD ANALYSIS & CRITICAL CONTROL POINTS What is HACCP ? Hazard Analysis Critical Control Points (HACCP) is an internationally recognized method of identifying and managing food safety-related risk and, when central to an active food safety program, can provide your customers, the public, and regulatory agencies assurance that a food safety program is
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ISO 9362:2014 – BUSINESS IDENTIFIER CODES What is ISO 9362:2014? ISO 9362 defines a standard format of Business Identifier Codes (also known as SWIFT-BIC, BIC, SWIFT ID, or SWIFT code) approved by the International Organization for Standardization (ISO). It is a unique identification code for both financial and non-financial institutions. The acronym SWIFT stands for the Society for Worldwide Interbank Financial Telecommunication. The ISO has designated SWIFT as
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