Taktly by industry

Pick your industry. See the patterns Taktly catches.

Different regulators, different vocabulary, same failure modes. Taktly grades your CAPA, root cause, and DMAIC work against the exact patterns FDA / USDA / GFSI auditors cite in your segment.

Pharma & Biotech

Sterile fill-finish, biologics, vaccines, cell & gene, API, generics, CDMOs. Graded against 21 CFR 211, 21 CFR 820, ICH Q9 / Q10 / Q7, EU GMP Annex 1.

See the audit patterns

Medical Device

Class II / III devices, IVDs, combination products, implantables. Graded against 21 CFR 820 (QSR), ISO 13485, ISO 14971, MDR / IVDR.

See the audit patterns

Food Manufacturing

RTE, beverage, dairy, meat & poultry, ingredient, co-manufacturing. Graded against FSMA, HACCP, USDA FSIS, GFSI (BRCGS, SQF, FSSC 22000).

See the audit patterns