Delivering 
Regulatory
Excellence
100+ Satisfied Clients.
Empowering Pharma with Compliance Expertise.
Regulatory-Forward Approach
We stay ahead of evolving pharmaceutical regulations — from USFDA 21 CFR to EU GMP Annex updates — leveraging proven validation methodologies, qualification frameworks, and compliance strategies to keep your organization inspection-ready and globally competitive.
Deep Industry Expertise
With 13+ years of hands- on experience across QA, Analytical R&D, and Quality Control in USFDA and WHO- regulated environments, our team delivers validated systems, regulatory documentation, and quality-driven solutions across all areas of pharmaceutical operations.
Dedicated Ongoing Support
From laboratory establishment and equipment qualification to audit support and academic guidance — our experts are always available to address your compliance challenges, providing timely solutions that ensure uninterrupted regulatory success.
GMP / GLP Compliance
Establishment & Compliance
CSV / CSA
Equipment Qualification
QMS & Audit Support
Technical & Scientific Services
Training & Upskilling
Global Pharma Partner
Academic Guidance
21 CFR Part 11
ICH Q2(R1)
NABL Accreditation
Data Integrity
IQ / OQ / PQ
Powering Pharmaceutical Excellence Through Strategic Partnerships with Startups and Growing Organizations.
Our Mission
To provide affordable, regulatory-compliant quality and scientific solutions that strengthen pharmaceutical organization's systems — enabling operational excellence from laboratory establishment and equipment qualification to global regulatory approvals.
Our Vision
To be the most trusted compliance and scientific partner for pharmaceutical organizations in India and globally — delivering innovative validation, QA, technical, and training solutions that consistently exceed USFDA, EU GMP, and WHO standards.
Faster Results
40%
Average reduction in documentation and qualification timelines for clients versus building in-house teams
Enabling startups to raise $25M+ in venture funding.
Contact usYears Experience
13+
Combined pharmaceutical industry experience brought to every engagement — from lab setup to regulatory approvals
Tailored Compliance Solutions for Pharma Industries.
Pharma Industry Support
Comprehensive expert assistance across regulatory, technical, and operational needs — helping pharmaceutical organizations maintain compliance, resolve challenges, and achieve operational excellence at every stage of their growth.
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Establishment & Compliance
End-to-end guidance for setting up pharmaceutical operations — from lab infrastructure and SOP development to regulatory documentation and inspection-readiness aligned to USFDA, EU GMP, WHO, and Schedule M GMP standards.
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CSV / CSA & Digital Compliance
Computer System Validation and Computer Software Assurance for LIMS, CDS, and laboratory instruments — ensuring full 21 CFR Part 11 compliance, audit trail integrity, and reliable digital operations in regulated pharmaceutical environments.
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Equipment & Utility Qualification
Structured IQ, OQ, and PQ qualification protocols for analytical instruments, HVAC, purified water systems, and critical utilities — meeting USFDA, EU GMP Annex 15, and WHO regulatory expectations.
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QMS & Audit Support
Quality Management System setup, CAPA management, OOS/OOT investigation, deviation handling, and regulatory audit preparation — including pre-inspection mock audits and post-inspection response writing.
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Technical & Scientific Services
Specialized technical and scientific expertise supporting pharmaceutical development, analytical laboratory operations, method validation, and scientific documentation — from AMV protocols to technical reports for regulatory submissions.
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Training & Upskilling Programs
Industry-focused GMP/GLP training and professional development programs tailored for QA, QC, and AR&D teams — equipping freshers and experienced professionals with the regulatory knowledge and practical competencies needed to excel.
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Partner for Global Pharmaceutical Companies
Reliable execution partner services for global pharma companies operating in India — delivering regulatory support, technical expertise, and project execution within the Indian pharmaceutical ecosystem.
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Academic Guidance
Structured mentoring and career guidance for pharmacy students and life sciences graduates — helping them navigate academic pathways, research opportunities, and build meaningful careers in the pharmaceutical industry.
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Our Clients Share Their Success Stories.
InPharma Solutions set up our entire QMS — SOPs, deviation systems, qualification protocols, and audit formats — and had us inspection-ready in under six months. We sailed through our first USFDA pre-inspection without a single critical observation. Their Establishment & Compliance support is truly world-class.
The Technical & Scientific Services team at InPharma delivered AMV protocols for our HPLC and ICP-OES methods that were technically flawless and ICH Q2(R1)-compliant. Our regulatory submission passed review on the first attempt. Exceptional knowledge and professionalism throughout.
InPharma handled our complete CSV and 21 CFR Part 11 implementation with a level of rigour I hadn't seen before. Their Digital Compliance team's systematic approach to data integrity, audit trail validation, and documentation saved us months of internal effort and gave us full confidence for our US market entry.
The Experts Empowering Your Compliance Journey.
The Ultimate Pharma Compliance Resource.
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