Why DIQC Life Sciences

DI Quality Certification Services Pvt. Ltd. can support your organization to improve organizational performance and mitigate risks via ISO 13485 and applicable regulatory standards.

• Medical devices industry is a growing on the paramount.
• There is huge demand for the product to be tested by competent laboratories for to meet the manufacturing requirements and saturator requirements for product approval and release.
• Accredited laboratories with competent expertise in meeting testing requirements as manufacture and regulator need is the huge gap.
• Testing need will go raise up to 50% of existing upon MDD shift
• DIQC-LS has vision to the establish a topnotch facilities and expertise in the team to fulfills the customer needs and requirements of notified body

Lifesciences Division

Business Opportunity

• Medical devices manufactures Class I,II,III with scope of ISO 13485, CE, MDD,MDR all over India and abroad
• Pharmaceutical Industries . IP, USP, BP, CDSCO