About Us
About Us
Farmacious is a specialized consultancy focused on Computerized System Validation (CSV) and GxP Compliance Operations for the pharmaceutical industry.
Backed by 22+ years of experience, our founder has led major initiatives across Formulation, API, Oral Dosage, Inhalation, and Topical product segments.
He has been a pioneer in setting up CSV Master Plans and IT Quality Systems, and has successfully designed, validated, and implemented 50+ computerized systems, completing 300+ projects across global markets including US, EU, Australia, and Africa.
With a strong track record in regulatory inspections like USFDA, EU GMP, TGA, ANVISA, WHO, CDSCO, and NAFDAC, and driven by deep domain expertise and proven leadership, Farmacious delivers compliance-driven digital solutions.
About Us
Farmacious is a specialized consultancy focused on Computerized System Validation (CSV) and GxP Compliance Operations for the pharmaceutical industry.
Backed by 22+ years of experience, our founder has led major initiatives across Formulation, API, Oral Dosage, Inhalation, and Topical product segments.
He has been a pioneer in setting up CSV Master Plans and IT Quality Systems, and has successfully designed, validated, and implemented 50+ computerized systems, completing 300+ projects across global markets including US, EU, Australia, and Africa.
With a strong track record in regulatory inspections like USFDA, EU GMP, TGA, ANVISA, WHO, CDSCO, and NAFDAC, and driven by deep domain expertise and proven leadership, Farmacious delivers compliance-driven digital solutions.
Ankit Kumar Jain
Founder & Partner
About the Founder
Ankit Jain is a Pharmacy graduate with over two decades of rich experience in pharmaceutical Quality Systems. He brings a unique combination of expertise in pharmaceutical operations and IT systems. He began his career in 2003, focusing on core pharmaceutical quality functions, and expanded into IT systems in 2012. He has played a vital role in building and strengthening Computerized System Validation (CSV) practices in line with GAMP 5 principles. His work includes developing Validation Master Plans (VMPs) and procedures to ensure robust control over GxP-relevant IT systems.
Ankit has contributed to the successful implementation of a wide range of GxP computerized systems, including TrackWise®, LIMS, ERP, chromatography data systems, Document Management Systems (DMS), Learning Management Systems (LMS), Risk Management Systems (RMS), and Robotic Process Automation (RPA). His approach consistently balances regulatory compliance with business efficiency
During his tenure at Arcolab, he was part of the senior leadership team that shaped the organization’s quality vision. He led key digital transformation initiatives such as paperless validation and secured, organization-wide access to controlled documents.
His professional journey also includes significant experience with Cipla, Ranbaxy, Sun Pharma, Strides, and Glenmark. In these roles, he worked across various quality domains including Quality Operations, Quality Systems, Qualification and Validation, Audit and Compliance, and Batch Release
Ankit is a Certified Quality Auditor from the American Society for Quality (ASQ) and a certified trainer. He has effectively represented systems and processes before regulatory bodies with clarity, confidence, and credibility.
GxP SYSTEMS
ADVANTAGE GxP SYSTEMS
- Digitally signed entries and records using Class-3 Digital Signature Certificates
- Audit-ready documentation
- Seamless accessibility
- Find document and search content in no time
Hands-on experience in validating and integrating systems like:
eQMS, SAP, LIMS, LMS, DMS, CDMS, PLC, IPC, and more. This means:
Minimal operational disruption
Stronger cross-system compliance
Enhanced Control over process
Our unique blend of deep pharma knowledge + strong IT expertise helps you:
Establish collaboration between QA and IT
Implement smart, scalable, and compliant systems
Future-proof your digital infrastructur
Work with experts who’ve successfully implemented technologies like RPA, Microsoft BizTalk, and Big Data in regulated environments, so you save time, reduce manual errors, and increase efficiency.
With over a decade of proven CSV expertise, we help you:
-Avoid common pitfalls
-Pass audits smoothly
-Get your systems right the first time
Not only operate with full efficiency and reliability, but also confidently showcase your digital systems and win trust of regulators.
- Schedule a Consultation
Schedule a one-on-one consultation with our experts to explore how Farmacious can support your CSV and GxP compliance projects. No obligation—just clarity and guidance.
