It’s our end-to-end procurement model connecting buyers with certified manufacturers worldwide to ensure quality, compliance, and continuity of supply. For manufacturing standards, see WHO Good Manufacturing Practices (GMP).
About Us – Global Pharma Sourcing Specialists
From India to the World — Bridging Pharma Excellence and Global Trust.
At Cureinfirmity Pharmaceuticals (CI Pharma), we are Global Pharma Sourcing Specialists, committed to ensuring quality healthcare transcends borders.
Introducing the founder
Our Story
As Global Pharmaceutical Sourcing Specialists, Cureinfirmity Pharmaceuticals delivers compliance-driven, high-quality pharmaceutical solutions worldwide. Founded by Mayank Mittal, whose deep roots span retail to distribution, CI Pharma transforms the global sourcing experience—turning challenges of unpredictability into dependable international partnerships.
Our Mission
To provide reliable, high-quality pharmaceutical sourcing and trading solutions that enable our partners to deliver life-saving medicines to patients worldwide.
Our Vision
To be the world's most trusted pharmaceutical trading partner, setting new standards for quality, innovation, and customer service in the industry.
Our Values
Integrity, excellence, innovation, and customer-centricity guide every decision we make and every relationship we build.
Trusted Industry Relationships
Mayank Mittal
Founder & CEO
Rohit Kumar
Trusted Partner
Wasif Ahmed
Trusted Partner
Frequently Asked Questions
Because we combine supplier due diligence, regulatory alignment, QA documentation, and logistics oversight—so partners get compliant, reliable deliveries across markets. Explore our end-to-end capabilities on the Services page.
Through documented QA processes, GMP-aligned audits, certificates of analysis, stability data (where applicable), and regulator-ready dossiers (CTD/eCTD). We maintain supplier scorecards and update controls regularly.
Yes. India is a core hub, and we maintain a growing global network. Suppliers are evaluated on certifications, capacity, and regulatory history to match each target market.
Yes. We prepare/validate CTD/eCTD dossiers, variations, and market-specific documentation, reducing approval friction while maintaining compliance.
Inquiry → supplier shortlisting → QA/reg checks → negotiated terms → production oversight → QC release → compliant export, customs, and delivery. Quotes in ~24–72 hours for standard requests.