Sidapharm Achieves MDSAP – ISO 13485 Certification

We are proud to announce the successful completion of our MDSAP – ISO 13485 certification for the Brazilian and Canadian markets.

This significant milestone is a clear reflection of our unwavering commitment to quality, safety, and regulatory compliance in the field of medical devices.

What is MDSAP?

The Medical Device Single Audit Program (MDSAP) allows a single regulatory audit to satisfy the requirements of multiple jurisdictions, including the United States, Canada, Brazil, Japan, and Australia. Certification to the ISO 13485 standard, in combination with MDSAP requirements, ensures that our products meet the highest international standards for quality and safety.

Why is this important?

This certification:

• Expands our presence in global markets, enabling us to reliably serve our customers in Brazil and Canada.
• Strengthens our credibility with partners, healthcare providers, and regulatory authorities.
• Demonstrates our ongoing commitment to quality excellence and innovation.

A Big Thank You to Our Team!

This achievement would not have been possible without the dedication, collaboration, and professionalism of our entire team. We sincerely thank every member of the Sidapharm family who contributed to reaching this goal with consistency and determination.

At Sidapharm, we continue to invest in quality and move confidently toward the future of global healthcare