ISO Certification Process

The is an internationally recognized standard that sets out requirements for a quality management system. For pharmaceutical companies, this certification is particularly important, as it ensures that their products are manufactured in compliance with international standards. To obtain ISO certification, a pharmaceutical company must undergo a rigorous auditing process, which includes a review of the company's quality management system and an assessment of its manufacturing processes. Once the company is deemed compliant, it is issued an ISO certificate, which is valid for a set period of time. This certificate serves as proof that the company's products meet international quality standards.