La norme internationale ISO/CEI 17025:2017 précise les normes générales de travail des laboratoires de manière compétente, impartiale et cohérente. Il fixe les critères fondamentaux d’exécution des essais et des étalonnages. Les lignes directrices comprennent les essais et l’étalonnage effectués au moyen de procédures normalisées, non normalisées et en laboratoire.

An FDA certificate, also called an “FDA label”, is an official seal of approval. It must be placed on any product that has been approved by the FDA. If you are looking to sell your product in the United States, then chances are your product will require FDA certification because all products sold in the United States must meet certain standards and regulations.

Halal fait référence à une large gamme de produits et de services que les musulmans utilisent régulièrement. Les clients musulmans préfèrent les articles qui adhèrent à la loi islamique.

Delegates will be prepared to draft an audit report on the correct implementation and maintenance of a management system after completing this ISO 50001 training course. Delegates will also gain an understanding of auditing procedures in accordance with ISO 19011.

ISO – International Organization for Standardization is an independent organization that sets out standards for businesses in terms of quality, safety, and environment of the management system. IAS audits and issues certification towards such standards.

For a product to be accepted into the European business market, it must have CE certification. CE certification guarantees that the product and its packaging meet European safety and quality requirements. CE Certification certifies to buyers that a product has been created in conformity with European health, safety, and environmental requirements.

GMP certification requirements include design validation, process validation, facility validations, personnel training requirements, lot release testing requirements, complaint handling procedures, and equipment maintenance/calibration requirements.

The IRCA accredited ISO Lead Auditor Training Courses are for corporate professionals who wish to further their careers by performing internal and third-party audits. Third-party certification bodies and corporate companies may hire individuals who have completed this ISO auditor training course as lead auditors to assure compliance with international standards.

La FDA est également chargée de réglementer la fabrication, la commercialisation et la distribution des produits du tabac afin de protéger la santé publique grâce à un contrôle approprié de ces produits.

La norme internationale ISO 13485 établit des critères pour les entreprises qui offrent des matériels médicaux et de l’équipement pour améliorer leurs systèmes de gestion de la qualité. Il précise les mesures de contrôle visant à réduire les défauts de fabrication et de fonctionnement du système. Cette norme garantit également que la qualité du matériel médical continue d’être améliorée.