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HACCP stands for Hazard Analysis and Critical Control Point. HACCP is a system that identifies critical points in the production chain at which controls can be applied to prevent or eliminate contamination by pathogens, including bacteria, viruses, parasites, and other microorganisms. HACCP Certification also attempts to prevent problems with pesticides, food allergens, decomposition, and undesirable flavors or odors.

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Boost up your auditing skills and enhance your confidence to conduct a full audit of the Environmental Management System (EMS) based on ISO 14001 with the iso 14001 lead auditor training course. Improve your knowledge and skills to plan, conduct, as well as to manage an audit of EMS in compliance with ISO 14001. Also, develop your existing auditing skills and become an IRCA certified ISO 14001 Lead Auditor with this course

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The ISO 9001 lead auditor certification course provides delegates with the skills and knowledge required to audit ISO 9001:2015 quality management systems. This ISO 9001 training course is designed for experienced quality professionals who wish to become ISO 9001 lead auditors.

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CE stands for “ConformiteEuropene,” which translates to “European Conformity.” This mark is required for products to be accepted into the European business market. CE certification ensures that the product and its packaging comply with European safety and quality standards.

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ISO 9001 certification is one of the most widely recognized quality management system standards in the world. The standard is used by organizations in a wide range of industries, and achieving ISO 9001 certification  can help businesses improve their operations, expand their customer base, and grow more profitably.

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ISO certification is a third-party verification that a business or organization meets the international standards set by the International Organization for Standardization (ISO). ISO is an independent, non-governmental organization that develops and publishes international standards for various industries and sectors.

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The international standard ISO 13485 provides requirements particularly to improve the quality management ISO 13485 Certification system of the organizations that provide medical devices and equipment. It specifies control measures to reduce operational errors in the manufacturing process and system.