Pharma packaging manufacturer
TiO2 for Pharmaceutical Packaging Suppliers
Pharmaceutical packaging demands USP / EP / JP pharmacopeial-grade TiO2 with batch-by-batch heavy metal testing.
Typical volume
50–1000 t/year
Qualification cycle
12–16 weeks (pharma supply qualification extended)
Business context
Pharmaceutical packaging suppliers produce HDPE/PP pill bottles, PVC/PVDC blister packs, secondary cartons. TiO2 used for opacity (protecting drugs from light) and white aesthetic.
Procurement challenges
- 01ICH Q3D elemental impurity compliance (Pb, Cd, As, Hg)
- 02USP/EP/JP pharmacopeial documentation
- 03GMP supply chain qualification (Pharmaceutical-grade audits)
- 04Batch-by-batch testing requirements
What SEMITI brings
SEMITI 996, 902, A100 with batch heavy metal testing certificates. ICH Q3D compliant grade documentation. GMP-quality packaging and handling.
Recommended SEMITI grades for pharmaceutical packaging suppliers
SEMITI 996
rutile · chloride
Universal Rutile
Our flagship chloride-process rutile — high tinting strength and broad compatibility for coatings, plastics, and inks.
SEMITI 902
rutile · chloride
Universal Coatings Rutile
Universal coatings-grade rutile — the global reference for waterborne and solventborne paints.
SEMITI A100
anatase · sulfate
Universal Anatase
Universal anatase grade for inks, paper, fiber and rubber — bright white with soft, easily-dispersed crystal.
Related technical guides
Common questions
Can SEMITI 996 meet USP <232> heavy metal limits?+
Yes — SEMITI 996 typical batch: Pb < 5 ppm, Cd < 1 ppm, As < 2 ppm, Hg < 1 ppm. All meet ICH Q3D Class 1 limits for oral/parenteral drug products.
Talk to us about your pharmaceutical packaging suppliers TiO2 procurement
Send us your current grade, volume, and qualification process. We'll respond with a substitution analysis and sample plan within 48 hours.