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ICFC
SS 620

SS 620 Good Distribution Practice for Medical Devices (GDPMDS)

SS 620 is the Singapore Standard for Good Distribution Practice for Medical Devices (GDPMDS). It ensures devices keep their quality and safety through storage, handling, delivery and traceability. Medical device dealers commonly need it for their licensing.

Group

Singapore Standards and Schemes

Standard or scheme
SS 620
Enterprise Singapore (Singapore Standards)
Type
Certifiable
Certificate issued by an accredited certification body
Group
Singapore Standards and Schemes
View all 7 →
Funding
Not on the EDGE Standards list
Non-grant engagement

What is SS 620?

SS 620 sets requirements for a quality management system for the storage, handling, delivery and traceability of medical devices in the distribution chain.

Who is SS 620 for?

Medical device importers, wholesalers, distributors and warehouses in Singapore.

Not on the EDGE Standards list

No grant found when checked - Non-grant engagement

We did not find this standard on the EDGE Standards list when we checked. Ask us about non-grant options or other schemes that may apply.

About EDGE →Information checked 11 October 2026. Grant decisions are made by the funding agency.

Impartiality

Impartiality comes first. Every engagement begins with a conflict-of-interest check. We keep consulting and auditing roles separate, and our auditors never audit, on behalf of a certification body, an organisation that ICFC has consulted on the same scope within the period set by that body.

Our certification role

We do not certify organisations ourselves; certificates are issued by accredited certification bodies or scheme owners.

How we help

01

Third-party audits

Third-party certification audits for SS 620 are delivered by our auditors on behalf of accredited certification bodies. The certificate is issued by the certification body, not by ICFC.

02

Second-party audits

Supplier and partner audits against SS 620 on behalf of your organisation, with clear findings you can act on.

03

Internal audits

First-party internal audits of your good distribution practice for medical devices by experienced auditors, combinable with other standards in one integrated audit.

FAQ

Frequently asked questions