Frequently Asked Questions
Common questions about our pharmaceutical consulting and GxP compliance services.
What services does Sentria Life Science provide?
Sentria Life Science delivers end-to-end pharmaceutical consulting services including GxP compliance, Regulatory Affairs, Pharmacovigilance, Clinical Research Support, Computer System Validation (CSV), Medical Writing, SOP Development, Quality Management Systems, and inspection readiness solutions for pharmaceutical, biotechnology, CRO, CDMO, and healthcare organizations worldwide.
Which regulatory standards do you support?
Our solutions are aligned with FDA, EMA, MHRA, CDSCO, ICH, WHO, and PIC/S expectations — delivering risk-based, inspection-ready outcomes with global regulatory expertise across every engagement.
Do you work with startups as well as large enterprises?
Yes. We offer flexible engagement models designed to support emerging biotech startups, SMEs, and established multinational pharmaceutical organizations at every stage of the product lifecycle.
How can I request a consultation?
You can fill out our contact form, email us at sentrialifescience@gmail.com, or call +91 820 073 6086. Our team will respond promptly to discuss your compliance and consulting needs.
What is your approach to GxP audits?
We conduct risk-based GxP audits across GMP, GCP, GLP, GDP, and GVP domains, identifying gaps and providing actionable recommendations to ensure sustainable compliance and inspection readiness.
Do you provide pharmacovigilance and QPPV services?
Yes. Our evidence-based pharmacovigilance services include ICSR case processing, literature searches, aggregate reporting, signal management, risk management, QPPV services, and medical information support — all aligned with FDA, EMA, MHRA, WHO, and ICH requirements.