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SS 620: 2016 GDPMDS in Singapore is a critical standard that outlines the stringent requirements distributors and importers must follow to ensure the quality, safety, and integrity of medical devices throughout the entire distribution lifecycle. By implementing SS 620: 2016 GDPMDS in Singapore, organizations can maintain strict control over storage, handling, transportation, and documentation processes, ensuring that medical devices remain safe and effective for end users. This standard also helps companies strengthen regulatory compliance and align with the expectations set by Singapore’s Health Sciences Authority (HSA). Adopting SS 620: 2016 GDPMDS in Singapore not only enhances operational reliability but also builds trust with healthcare providers, manufacturers, and patients by demonstrating a commitment to high-quality distribution practices.
SS 620: 2016 GDPMDS in Singapore will replace the HSA Good Distribution Practice for Medical Devices – Requirements, Revision 2.1 (HSA GDPMDS TS-01, R2.1) as the certification standard from 9 November 2020 onwards.
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