Question 1

How do I verify a certification?

Accepted Answer

Every certification comes with a certificate number and issuing body. Contact us with your NDA/CDA in place and we'll provide the full certificate, audit report, and chain-of-custody documentation for your compliance team to review.

Question 2

What is a DMF and why does it matter?

Accepted Answer

A Drug Master File (DMF) is a confidential submission to the FDA describing facilities, processes, or materials used in manufacturing. DMF Type III covers packaging materials. Having an active DMF means pharmaceutical customers can reference it in their ANDA/NDA filings, saving 6-12 months of supplier qualification.

Question 3

Are certifications valid globally?

Accepted Answer

FDA and ASTM are US-focused but recognized globally. ISO, FSC, GRS, and ISCC are international standards. EN 13432 is EU-specific. EU PPWR is EU regulation. We maintain certifications for all major markets: North America, EU, and Middle East.

Question 4

How often are certifications renewed?

Accepted Answer

ISO certifications are audited annually with full recertification every 3 years. FSC is audited annually. FDA DMF is updated as materials change. GRS and ISCC PLUS are audited annually. All certificates are current and active.

Certifications You Can Trust.<br/>No Greenwashing. No Vague Claims.

Questions About Our Certifications

Need certification documentation for your compliance team?