fayemunoz's blog

What is ISO Lead Auditor Training?
ISO Lead Auditor Training is a program that provides participants with the skills and knowledge necessary to conduct ISO lead audits. The program covers topics such as auditing principles, auditing techniques, and auditing standards. It also teaches participants how to prepare and conduct an audit, and how to write an audit report.
Importance

Overview of the ISO 45001 Standard
ISO 45001 is an international standard for occupational health and safety management systems (OHSMS). It was published in March 2018 and replaces the former OHSAS 18001 standard. Certification to ISO 45001 demonstrates that an organization has implemented a comprehensive OH&S management system that meets the requirements of the standard. Certification to ISO 45001 is not mandatory, but it can be an important way to demonstrate that an organization is committed to safety and has implemented a robust OH&S management system.

What is ISO 20000 Certification?
ISO 20000 is a worldwide standard that specifies the criteria for IT service management. Organizations that achieve ISO 20000 certification have demonstrated that they have implemented a best-practice service management system (SMS) and are capable of providing consistent, high-quality IT services.
Why ISO 20000 Certification?

What is ISO 9001 Lead Auditor Training?
ISO 9001 Lead Auditor Training is a program that teaches individuals how to audit organizations for compliance with the ISO 9001 quality management standard. The course covers all aspects of the auditing process, from planning and conducting a lead audit to issuing a report.
Importance

What is ISO 17025 Certification?
ISO 17025 is a quality management system standard that specifies the requirements for the design, development, implementation, operation, and maintenance of a laboratory quality management system. Laboratories that achieve ISO 17025 certification demonstrate that they are capable of consistently producing accurate and reliable test and calibration results.
Why is ISO 17025 Certification Important?

What is BRC?
The British Retail Consortium (BRC) is a global organization that sets voluntary standards for the food industry. Their goal is to ensure that the food products that are sold in stores are safe and meet certain quality requirements. To achieve this, the BRC has developed a certification program that companies can pursue to show that they comply with the organization's standards.
What is BRC Certification?

What is cGMP?
cGMP stands for "Current Good Manufacturing Practices." It is a set of regulations enforced by the FDA that ensure pharmaceuticals are manufactured safely and consistently. To be certified as cGMP-compliant, a facility must meet rigorous standards for quality and safety.
What is cGMP Certification?
cGMP certification is a voluntary recognition through which a pharmaceutical company can demonstrate that it meets the FDA's cGMP regulations. To become certified, a company must undergo an extensive audit of its manufacturing process and facilities.

Defining ISO 14001
The ISO 14001 standard is a globally known standard for environmental management systems. It provides a framework that organizations can use to improve their environmental performance. ISO 14001 Certification ensures that an organization has implemented an effective environmental management system and meets the requirements of the standard.
Importance

Overview of ISO 27001 Certification
An ISO 27001 Certification is an internationally recognized certification demonstrating that a company has implemented and follows a comprehensive information security management system. The ISO 27001 standard is based on a number of best practices for information security management, including risk assessment, security control implementation, and continual improvement.

What is CE Certification?
CE certification is the process of verifying that a product meets the essential health and safety requirements set by the European Union. The CE mark is proof that a product has been assessed and meets these requirements. Products carrying the CE mark can be sold in all EU member states. The CE Marking Directive sets out the specific requirements products must meet in order to be CE certified. These requirements cover a wide range of issues, including product safety, electromagnetic compatibility, environmental impact, and health and safety.