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Technical Support: support@ssiexport.com
Call: +91 9040 479 033
The Global Standard in
Pharmaceutical Visual Inspection
For over 15 years, SSI has been at the forefront of particulate defect preparation, inspection methodologies, and regulatory compliance, delivering industry-leading expertise across these critical areas.
Our Story
SSI (Siddhi Sai International) was founded in 2020 to solve a specific problem: every injectable drug sold anywhere in the world has to pass 100% visual inspection before release, and majority of manufacturers don’t have the defect kits, training, or in-house expertise to do it reliably.
We built that capability in India first, where we captured over 50% of the domestic market for visual inspection qualification. In 2023, we expanded internationally as SSI, and now serve pharmaceutical, biotech, and CDMO companies across APAC and beyond.
Our leadership team has 20+ years of experience in pharmaceutical visual inspection and regulatory compliance, backing every defect kit, inspection booth, and audit-readiness program we deliver.
Our Journey
A timeline of milestones that shaped SSI into what it is today.
Foundation
Gained traction with 20+ leading pharma firms through word of mouth, becoming known for kit reliability and quality
2021
Industry Recognition
Launched Siddhi Sai International to meet growing global demand, adopted by 50+ major pharma companies worldwide
2025
Expansion
2020
Siddhi Sai Global founded in India to address critical gaps in visual inspection qualification
Early Adoption
2022
Selected by PDA India Chapter for live demos and training. Expanded into hands-on workshops for pharma QC professionals
Going Global
2026 –
Working with 90+ injectable drug manufacturers across 10 countries, we are establishing regional bases to better serve customers worldwide
Our Journey
A timeline of milestones that shaped SSI into what it is today.
2020
Foundation
Siddhi Sai Global founded in India to address critical gaps in visual inspection qualification
2021
Early Adoption
Gained traction with 20+ leading pharma firms through word of mouth, becoming known for kit reliability and quality
2022
Industry Recognition
Selected by PDA India Chapter for live demos and training. Expanded into hands-on workshops for pharma QC professionals
2025
Going Global
Launched Siddhi Sai International to meet growing global demand, adopted by 50+ major pharma companies worldwide
2026 -
Expansion
Working with 90+ injectable drug manufacturers across 10 countries, we are establishing regional bases to better serve customers worldwide
Our Vision
To be the global leader in visual inspection qualification, delivering cutting-edge solutions tailored to industry needs.
Our Mission
To provide world-class visual inspection solutions that enhance pharmaceutical quality control and regulatory compliance.
Our Core Values
Precision & Compliance
We maintain the highest standards of accuracy and regulatory adherence in all our solutions.
Innovation
Continuous improvement drives our development of industry-leading inspection technologies.
Customer Focus
We build long-term partnerships by understanding and addressing each client’s unique needs.
Built for Regulatory Compliance
We are committed to ensuring the safety and integrity of parenteral products through compliance with global standards and fulfilling all regulatory requirements such as USFDA, MHRA, EU, TGA etc.
Watch our Corporate Video to see how we support our customers
Our Leadership Team
Experts with 18+ years of visual inspection & compliance experience
Pritam Pany
Chief Business Officer
Kalpesh Patel
Head of Engineering
Ms Sneha Nene
Head of Quality
Mr Munib Pathan
Senior Scientist
Mr Pradip Desai
Junior Scientist
Mr Girvat Thakor
Junior Scientist
Rahul Suryavanshi
Junior Scientist
Vikram Gohil
Junior Scientist
Rameswari Satpathy
Marketing Associate
Shakti Prasad Jena
Biz Ops Associate
Our Advisors
Debashisa Panda
DGM – Alembic Pharmaceuticals
Technical Advisor
Brig. Dr. D. B. Pany (Retd)
Strategic Advisor
Why Leading Pharma Companies Choose SSI
Years of Domain
Expertise
Hands-on experience across Production and QA teams in sterile manufacturing environments.
Engineering + Scientific
Depth
From calibrated particle insertion (50-5,000 microns) to AVI validation and building USP <1790> compliant systems.
Regulatory-Ready
by Design
Audit-aligned documentation, traceable defect libraries, and validated visual inspection frameworks.
Trusted by 90+ Pharmaceutical Manufacturing companies worldwide
90+
Injectable Manufacturers Served
20 Years
Defect Library & Expertise
11
COUNTRIES
ISO 9001
CERTIFIED
Our Valued Clients
Trusted by organizations committed to the highest standards of pharmaceutical quality and compliance.
Trusted by Leading Pharma Companies
Hear directly from pharmaceutical professionals who trust our solutions
to deliver quality, reliability, and performance.
Get in Touch
Ready to Place an Inquiry?
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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