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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.

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.
Importance

What is CE marking?

What is ISO 27001 Lead Auditor Training?
ISO 27001 Lead Auditor Training is an intensive program that provides participants with the skills and knowledge necessary to perform lead audits for organizations that have implemented the ISO 27001 Information Security Management Standard. The course is designed for experienced auditors who wish to become certified as ISO 27001 Lead Auditors.
Importance

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 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.

What is Meant by a Quality Management System?
A quality management system (QMS) is a set of business processes and procedures that helps an organization ensure that it meets the highest quality standards. ISO 9001 certification is an internationally recognized certification for quality management systems. Having this certification can help your business attract new customers, improve employee morale, and boost profits.
Importance