Effective Training Programs
Global Medical Device QMS Certification
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We at DI Quality Certification Services Pvt.Ltd. provide Audit and Certification services of Third party Audit, Certification, Surveillance and Recertification services for ISO 9001 (Quality Management System) and ISO 13485 (Medical Devices QMS).
DI Quality Certification Services Pvt. Ltd. has a qualified and skilled team to nurture and impart knowledge, conduct trainings, courses and workshops regarding the national and international standards and regulations of Medical Devices. Our training courses are developed by subject experts to help client organizations to enable sustainable business development and competitive advantage.
DI Quality Certification Services Pvt. Ltd. (DI QCS) is an independent legal entity (CIN U73100TN2021PTC144132). DI QCS provides third party certification services (Quality Management System certification in ISO 9001 and ISO 13485) and training services. DI QCS is solely responsible for all its certification activities. DI QCS is responsible for, and retains authority for its decisions relating to certification, including the granting, refusing, maintaining of certification, expanding or reducing the scope of certification, renewing, suspending or restoring following suspension, or withdrawing of certification.
System Certification is third party stamp of approval that an organization's management system conforms to specified standards. Certification enables companies to enhance their reputation and open up new markets, or simply ensure that they are able to operate.
We are committed to comply with requirements of ISO 17021, applicable International Accreditation Forum Mandatory Documents (IAF MDs), and other applicable normative documents.
Our competent team aims to provide efficient and excellent audit and certification services to our client's management systems in the medical industry, so as to fulfil their requirements of ISO 13485 (Medical Devices QMS) standards.
DI Quality Certification Services Pvt. Ltd. can support your organization to improve organizational performance and mitigate risks via ISO 13485 and applicable regulatory standards.
Your organization can benefit from our extensive pool of experts beyond theoretical knowledge, our team has practical experience in fields non-active, active and in-vitro medical device auditing & certification.Our network of technical experts provides additional support in the form of industry and specialist knowledge.
QMS certification allows systematic application of management policies, procedures and practices to the tasks of analysing, evaluating, controlling and monitoring risk
Organization can leverage their certified QMS status for a seamless transition into specialized certifications such as EU MDR, EU IVDR, Indian MDR, USFDA etc.
Quality management certification provides a competitive edge in market. It communicates high standards of products and services to medical device industry.
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New Door No:18, 86th Street, 18th Avenue,
Ashok Nagar, Chennai – 600083,
Tamil Nadu , India
2nd Floor, office number
232,
VTP Trade Park, Katraj-Hadapsar Road,
Undri, Pune-411060,
Pune , India
