WHO-GMP Certified Commercial Supply

VEERIX-TRYPSIN Tablets Contract Manufacturing & CDMO

Veerix Biotech is a WHO-GMP certified third-party pharmaceutical manufacturer and CDMO partner producing VEERIX-TRYPSIN Tablets (TRYPSIN, BROMELAIN & RUTOSIDE TRIHYDRATE TOTAL PROTEOYTIC ACTIVITY NOT LESS THAN 1095 FIP UNITS / TABLETS (PAPAIN METHOD) ENTERIC COATED TABLET) within the Others therapeutic class, with complete Certificate of Analysis (CoA), stability studies, and regulatory dossier compliance for domestic Indian and global export markets.

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Technical Specifications & Formulation Details

Product NameVEERIX-TRYPSIN Tablets
Active CompositionTRYPSIN, BROMELAIN & RUTOSIDE TRIHYDRATE TOTAL PROTEOYTIC ACTIVITY NOT LESS THAN 1095 FIP UNITS / TABLETS (PAPAIN METHOD) ENTERIC COATED TABLET
Therapeutic SegmentOthers
Dosage FormTablets
Primary Packaging10*10 Tablets
Quality StandardIP / BP / USP Pharmacopeial Standard, WHO-GMP Certified
Manufacturing FacilityTahliwal Industrial Area, Tehsil Haroli, Una, Himachal Pradesh & Coimbatore, Tamil Nadu
Regulatory DocumentationBatch Release CoA, Method of Analysis (MOA), Accelerated & Real-time Stability Data, CTD Module 3

Commercial Supply Capabilities for VEERIX-TRYPSIN Tablets

Veerix Biotech provides end-to-end commercial supply and technical scoping for VEERIX-TRYPSIN Tablets in the Others class. From pre-formulation screening and pilot batch validation to automated blister packaging, serialisation, and multi-market regulatory clearance, our direct facilities and audited partner network ensure seamless execution.

  • Custom private label packaging with brand foil printing and anti-counterfeit features
  • Batch volume scalability: from pilot validation batches to large-scale commercial export runs
  • Dedicated QA/QC release testing including HPLC assay, dissolution testing, and microbial limits
  • Strict confidentiality with mutual non-disclosure agreement (NDA) upfront
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