Explore WHO-GMP certified oral solid dosage forms, sustained-release matrix tablets, sublingual ODTs, and specialized prescription therapeutics.



































Get verified factory pricing, PCD franchise terms, and COA dossiers directly.
All pharmaceutical tablet suppliers on TIS Nexus operate under WHO-GMP, cGMP, and ISO 9001:2015 certifications. Many facilities also hold international regulatory accreditations including USFDA, EU-GMP, PIC/S, NAFDAC, and PPB Kenya for export supply.
Yes. Verified contract manufacturers on TIS Nexus offer end-to-end PCD Pharma franchise, third-party manufacturing, custom tablet embossing, formulation development, stability testing, and private-label packaging (Alu-Alu, Blister, Strips, and Bottles).
Every batch is dispatched with comprehensive regulatory documentation, including Certificate of Analysis (COA), Batch Manufacturing Records (BMR), Finished Product Specifications, Stability Data (Zone IVb), and Common Technical Document (CTD / ACTD) dossiers for export registration.
For domestic third-party manufacturing, commercial batch MOQs generally start from 50,000 to 100,000 tablets per formulation. For export shipments, custom production runs typically require 100,000 to 500,000 tablets with bilingual packaging options.
TIS Nexus rigorously verifies every manufacturer's drug licenses (Form 25/28), WHO-GMP certificates, GST registration, and audited factory credentials. Direct factory pricing ensures transparent, reliable, and compliant healthcare supply chains.
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