At Sterinzo Pharma Technologies, we empower pharma organizations from emerging innovators to global leaders by delivering strategic, operational, and regulatory solutions designed for modern healthcare challenges.
Identifying, evaluating, and partnering with suitable third-party service providers (CRO & CMO) to outsource pharmaceutical activities like Formulation development, Analytical method development & validation, API or formulation manufacturing, Clinical trials & bioavailability/ bioequivalence (BA/BE) studies, Regulatory dossier preparation and submissions.
Bridges R&D, manufacturing, and regulatory affairs — ensuring that what’s developed in the lab can be manufactured reliably, compliantly, and cost-effectively at commercial scale.
Assisting pharmaceutical companies ensure their products, processes, facilities, and documentation comply with national and international regulatory requirements
Delivering niche knowledge and skills for critical assignments
At Sterinzo Pharma Technologies, we are more than consultants — we are your trusted collaborators in achieving pharmaceutical excellence. Here’s why leading pharma companies choose to partner with us:
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✅ Specialized Expertise in Pharma & Biotech
With deep-rooted expertise across oncology injectables, oral solid dosages, ophthalmic, biosimilars, cytotoxic facilities, and complex generics, we understand the unique technical, regulatory, and commercial challenges of modern healthcare markets.
✅ End-to-End Solutions Under One Roof
From product development, CMO/CRO management, regulatory affairs, compliance audits, to pharma talent solutions, we deliver comprehensive services tailored to your project’s life cycle — from R&D to commercialization.
✅ Regulatory Insight Across Global Markets
We help you navigate complex global regulations including USFDA, EU-GMP, WHO, TGA, and CDSCO India, with robust dossier preparation, regulatory strategy, inspection readiness support, and post-approval lifecycle management.
✅ Data Integrity & GMP Compliance Specialists
We strengthen your operational foundation by providing mock audits, data integrity gap assessments, GMP training programs, and compliance consulting to meet evolving regulatory expectations.
✅ On-Demand Pharma Talent Solutions
Access a network of highly qualified experts— from interim plant heads, validation managers, regulatory affairs professionals, to audit-ready QA/QC specialists — for short-term projects, audits, or specialized consulting roles.
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