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.
Highlights
Gap assessments and remediation aligned with FDA, EMA, WHO, and global guidelines.
Mock runs, documentation review, and CAPA guidance with ownership and timelines.
Sourcing for APIs, packing materials, reagents, chemicals, and impurities.
Radiology , neurology, cardiology, patient monitoring, surgery , Pulmunology , ENT ,Audiology, Psychiatry
Project Planning , Feasibility Studies , Design , Installation , Regulatory Compliance , Technology Transfer , Operational Support , Quality and control System , Handover Turnkey
Commercial, technical, and GMP risk evaluation to prioritize high-impact fixes.
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
EtaashLife 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.
More About EtaashLife
Services
01.
Feasibility, Engineering, Equipment sourcing, Construction, Commissioning, Validation, Documentation, Training & Support
02.
Project Advisory, Compliance, Training, Material Sourcing, Product Development, Quality, Operations.
03.
Monthly calendars, audits, documentation reviews, board meetings, trainings, advisory.
FAQ
FDA, EMA, WHO, MHRA, TGA, CDSCO, and others. Our auditors have global experience.
Yes. We provide prioritized findings and CAPA guidance with ownership and timelines.
Absolutely. We perform third-party audits and ongoing supplier qualification.
Discovery can begin immediately. Typical kick-off is within 1–2 weeks depending on scope.
