Diagnostica for Medical Reagents and Bioproducts received ISO 9001:2015 Certification

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Diagnostica for Medical Reagents and Bioproducts has completed the Surveillance audit and received a favourable recommendation for the continuation of their IAS-accredited ISO 9001:2015 Certification for Quality Management System (QMS).

The scope of the management system includes the Diagnostic Kit Medical Reagents & Bioproducts.

Apart from this, Diagnostica for Medical Reagents and Bioproducts can also apply for ISO 14001:2015 Certification for Environmental Management System (EMS) to implement eco-friendly manufacturing practices and achieve sustainable growth.

The organization can apply for ISO 41001:2018 Certification for Facility Management – Management System and ISO 13485:2016 Certification for Medical Devices – Quality Management System (MD-QMS) to provide clients, customers and stakeholders more hassle-free services to ensure their safety and well-being.  

Benefits of ISO 9001:2015 Standard for Diagnostica for Medical Reagents and Bioproducts

The following are the benefits of ISO 9001 for Quality Management System (QMS) for Diagnostica for Medical Reagents and Bioproducts. These are as follows :-

ISO 9001 enables Diagnostica for Medical Reagents and Bioproducts to streamline various business operations and processes to implement standardized procedures to minimize waste and optimize resource use.

ISO 9001 implementation ensures consistent quality control across Diagnostica for Medical Reagents and Bioproducts. Thus, it enhances reliability and quality to meet customer specifications and boost customer satisfaction. 

ISO 9001:2015 standard demonstrates Diagnostica for Medical Reagents and Bioproducts compliance with industry standards and regulatory requirements. It also helps the organization mitigate non-compliance risks and strengthen its credibility and market trustworthiness.

Conclusion

Diagnostica for Medical Reagents and Bioproducts received ISO 9001:2015 for Quality Management System (QMS) certification to demonstrate its commitment to quality and regulatory compliance in the medical device industry. Moreover, the certification strengthens the organization’s position in the global market by ensuring the safety and effectiveness of its products.

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