GMP Compliance
Gap assessments and remediation aligned with FDA, EMA, WHO, and global guidelines.
- FDA
- EMA
- WHO
Industry 4.0 Ready
Precision Audits. Innovative consultancy and reliable Turnkey solutions.
Over 30+ years of global GMP expertise. We help pharma manufacturers overcome the inertia of traditional practices—delivering risk-aware audits, inspection readiness, and optimized processes.
- Years of global GMP expertise
- 30+
- Years of global GMP expertise
- Offices: Mohali, Dubai, Syria
- 3
- Offices: Mohali, Dubai, Syria
- Guidelines we audit against
- FDA · EMA · WHO
- Guidelines we audit against
GMP Compliance
Gap assessments and remediation aligned with FDA, EMA, WHO, and global guidelines.
Our Trusted Partners
Pharmacy Consultancy · Advisory · Trading
Highlights
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Inspection Readiness
Mock runs, documentation review, and CAPA guidance with ownership and timelines.
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Sourcing
Sourcing for APIs, packing materials, reagents, chemicals, and impurities.
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Sourcing of hospital equipment
- Radiology
- Neurology
- Cardiology
- Patient monitoring
- Surgery
- Pulmonology
- ENT
- Audiology
- Psychiatry
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Turnkey Project Services
- Project Planning
- Feasibility Studies
- Design
- Installation
- Regulatory Compliance
- Technology Transfer
- Operational Support
- Quality and control System
- Handover Turnkey
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Risk Assessment
Commercial, technical, and GMP risk evaluation to prioritize high-impact fixes.
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Export promotion
The services offered support the export of pharmaceutical goods overseas by providing trade advisory, logistics coordination, export promotion, and documentation assistance. This ensures a smoother and more efficient process for companies looking to expand into international markets.
About
Who We Are
PillExpress is your partner in next-gen pharmaceutical audits. Our auditors bring 30+ years of global GMP experience and practical insight to help you modernize operations—without losing compliance rigor.
We combine deep regulatory knowledge with Industry 4.0 thinking to deliver clear findings, actionable CAPAs, and sustainable quality systems.
Services
What We Do
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01
Concept to commissioning model
Feasibility, Engineering, Equipment sourcing, Construction, Commissioning, Validation, Documentation, Training & Support
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02
Annual Compliance & Advisory Contract
Project Advisory, Compliance, Training, Material Sourcing, Product Development, Quality, Operations.
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03
Project Deliverables
Monthly calendars, audits, documentation reviews, board meetings, trainings, advisory.
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FAQ
Frequently Asked Questions
Which regulatory bodies do you support?
FDA, EMA, WHO, MHRA, TGA, CDSCO, and others. Our auditors have global experience.
Do you help with audit remediation?
Yes. We provide prioritized findings and CAPA guidance with ownership and timelines.
Can you audit CMOs and suppliers?
Absolutely. We perform third-party audits and ongoing supplier qualification.
How soon can we start?
Discovery can begin immediately. Typical kick-off is within 1–2 weeks depending on scope.
Clients We Serve
Pharmacy Consultancy · Advisory · Trading