Verify WHO-GMP status of every source facility before listing
We are the paperwork, the verification, and the cold box.
A NewMet Health does not manufacture medicines, and does not practise medicine. What we do is the unglamorous middle: confirming that a facility is certified, that a batch is what it claims to be, that a prescription is valid, that a country’s import rules are satisfied, and that a temperature-sensitive product arrives still fit to use.
What we do, and what we refuse to do.
Facilitation services in this category vary enormously in how carefully they operate. Stating the boundary publicly is the only way for a patient to hold us to it.
what we do
What we refuse to do
How a manufacturer earns a place on this site
Our supply base sits primarily in South Asia, where a mature generics industry produces to international standard for both domestic and export markets. Presence in that industry is not itself a qualification — these four criteria are.
Current certification
WHO-GMP certification verified as current, not historical. Certificates are re-checked each supply cycle rather than filed once.
Criterion 01
Export track record
Demonstrated regulated-market export history, which implies inspection exposure beyond the domestic regulator alone.
Criterion 02
Batch documentation
Willingness to supply a certificate of analysis tied to the specific batch shipped — not a generic product specification sheet.
Criterion 03
Cold-chain capability
For refrigerated products, validated packing and handling at the facility, with documented conditions from release to dispatch.
Criterion 04
How clinical content on this site is written
Health content that people act on carries a different obligation than marketing copy. These are the rules our own writers work to — published so you can check whether we are following them.
01
A named reviewer, with credentials
Every clinical page carries the name, qualification, and review date of the licensed professional who signed it off.
02
Gaps are shown as gaps
Where we lack verified data, the page says so. We do not substitute confident phrasing for a missing source.
03
Manufacturing claims stay separate from approval claims
WHO-GMP certification describes a facility. Regulatory approval describes a product in a jurisdiction. The two are never merged into one reassuring sentence.
04
Cost is never used as persuasion
Price may be stated as a fact when you ask. It is not used as an adjective to make a clinical decision feel easier.
05
No manufactured social proof
No testimonials, no star ratings on prescription medicines, no transformation photographs. None of it would be verifiable, so none of it appears.