A product will only be supplied when it has passed through IDA Foundation’s entire quality system and meets all required standards and relevant international requirements.

Samples of products are analysed for compliance with the quality standards of IDA Foundation and WHO/GMP. These standards often exceed requirements as outlined in the British Pharmacopoeia or the United States Pharmacopoeia.

To approve a product, we undertake the following actions:
• Assessment of product dossier, including product
  specifications, API quality and source, stability data,
  manufacturing procedure, bioequivalence study, packing, Certificate of Pharmaceutical Product (CoPP)
  according WHO certification scheme.
• Test sample for compliance to specifications.
• Development of labels and leaflets in one to four languages (English, French, Spanish and Portuguese).