Methodology

How product-listing information is checked and labelled

A product’s presence in a directory is an identification record—not independent proof of approval or equivalence.

Last updated: October 1, 2026

Minimum listing fields

We aim to record the represented active ingredient, brand name, manufacturer or supplier, strength, dosage form, pack information, image source and the date the data was checked.

Cross-checking

Names, strengths and pack details are compared across the supplied dataset and available source material. Ambiguities, duplicate-looking listings and source conflicts are flagged or excluded rather than silently resolved.

Regulatory verification

Unless a specific regulator record has been checked and cited for a product and jurisdiction, the page must not imply that the product is approved there. Regulatory status varies by country and should be confirmed with the relevant national medicines authority.

Equivalence and authenticity

Listing the same active ingredient does not establish pharmaceutical equivalence, bioequivalence, manufacturing quality, authenticity, safety or clinical effectiveness. MedFactHub does not perform laboratory testing or supply-chain authentication.

Questions about this policy?

Contact info@medicineforworld.com.bd.