General Inquiries: info@ssiexport.com
Technical Support: support@ssiexport.com
Call: +91 9040 479 033
We help fulfill injectable drug manufacturers comply with all regulatory requirements such as USP <1790>, <790>, EMA Annex-1, EP 2.9.20, EP 5.17.12, JP 6.06, MHRA, TGA and other global regulatory standards.
Trusted by
90+ Drug Manufacturers Globally
Comprehensive Defect kits with particle defects, cosmetic defects and good containers.
Visual Inspection Booth compliant with USP <1790> and optional 21 CFR Part 11 audit trails and electronic records
For qualification of leak testing equipment with ultra fine holes.
Precisely measured particles for in-house seeding and testing.
End-to-end support for setting up manual, semi- automatic, or automated visual inspection facilities.
Customized on-site training for Production and QA Teams.
ID of foreign particles using advanced techniques such as Confocal Microscopy, Raman Spectroscopy, FESEM – EDX, XRD, XRF, FTIR etc.
For testing mechanical function of your pharmaceutical equipment such as labelling, capping and packaging machines.
We participate in leading industry events, exhibitions, and regulatory forums worldwide.
Taipei, Taiwan
22 – 23 Sep 2026
Coex, Seoul
28 – 30 Oct 2026
Incheon, S. Korea
03 – 04 Nov 2026
Tokyo, Japan
16 – 17 Feb 2027
Explore real-world success stories demonstrating measurable improvements in pharmaceutical inspection processes.
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Hear directly from pharmaceutical professionals who trust our solutions to deliver quality, reliability, and performance.
Trusted by organizations committed to the highest standards of pharmaceutical quality and compliance.
Explore the latest advancements in inspection technology and their impact on pharmaceutical manufacturing.
SSI provides Visual Inspection Qualification Kits,Defect Kits, Knapp Kits, Manual Visual Inspection Booths, CCIT Positive Control samples and calibrated particles, along with consulting for facility setup, documentation review, inspector training and auditing, and particle characterization/analytical services for foreign-particle identification.
SSI supports clear and amber glass vials, lyophilized vials, pre-filled syringes, cartridges, ampoules, BFS containers/bottles, 3-piece ophthalmic bottles, IV bags, dry powder injections, FFS respules and all other difficult-to-inspect formats.
SSI can support the entire visual inspection lifecycle, including baseline/risk assessment, AVI feasibility review, facility/process development, FAT/SAT support, inspector qualification and requalification and supplying defect kits, inspection booths, CCIT positive controls, followed by particle identification services to reduce particle excursion.
Yes. SSI can supply qualification/defect kits for existing AVI systems and can support qualification, gap assessment and other parts of an established visual inspection program.
Let’s make your Visual Inspection Program Audit – ready
info@ssiexport.com
Phone
+91 9040 479 033
+91 9040 479 033
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