Compliance Automation

Automate your pharmaceutical compliance processes with real-time monitoring, reporting, and validation to stay audit-ready and fully aligned with global standards.

Call Us when you Need Help!
24/7 Support: +1 - 2093219310

Streamline Your Pharmaceutical Compliance

ZaiFi Tech’s Compliance Automation solutions help pharmaceutical companies simplify complex regulatory processes. Our system ensures end-to-end compliance with global standards, including cGMP, FDA 21 CFR Part 11, and EU GMP Annex 1, by automating monitoring, reporting, and validation tasks. This minimizes manual effort and human error—keeping your operations audit-ready at all times.

Data Integrity and Real-Time Monitoring

Our platform ensures data accuracy, traceability, and transparency throughout your compliance journey. With real-time monitoring and automated alerts, you can proactively identify deviations, maintain cleanroom standards, and respond instantly to compliance risks. Designed with pharmaceutical-grade security, our solution keeps your operations compliant and efficient.

Why Choose Us

At ZaiFi Tech, we go beyond compliance — we deliver smart, automated, and globally trusted solutions that empower pharmaceutical companies to meet regulatory standards with confidence. Our approach combines scientific precision, advanced technology, and international expertise, ensuring your operations stay efficient, compliant, and future-ready.

1
Global Compliance Alignment
100% aligned with FDA, EU GMP, and WHO compliance standards
2
Science-Driven Frameworks
Built on risk-based, science-driven CCS frameworks for precision and reliability in every process.
3
Real-Time Insights
Offers real-time compliance dashboards and reporting tools to keep you audit-ready anytime.

FAQs

There are many questions about the service, we have selected frequently asked questions about this service. If you do not see your answer, please contact us.

What is compliance automation?
Compliance automation uses technology to manage and monitor regulatory requirements automatically, reducing manual checks and ensuring consistent adherence to standards.
Is your solution suitable for small and mid-size pharma companies?
Yes. Our system is scalable and customizable to fit organizations of all sizes—from small manufacturing units to global enterprises.
How does compliance automation improve data integrity?
It eliminates manual data entry, ensuring that all records are accurate, timestamped, and tamper-proof, meeting FDA and GMP audit requirements.
Can it integrate with our existing systems?
Absolutely. Our platform integrates seamlessly with ERP, MES, and environmental monitoring systems for unified compliance management.

Why Choose Us?

Built for pharmaceutical industry compliance
Meets cGMP, FDA 21 CFR 211.28 & EU GMP Annex 1 standards
Based on risk-based, science-driven CCS frameworks
Trusted by global pharmaceutical leaders
Supported by teams in India & USA for global reach

Company Profile

Are you having health problems? Contact us today!

Address Business
4425 Fremont California USA
Contact With Us
Mail Us: contact@zaifitech.com
USA +1 - 2093219310
Working Time
Monday - Saturday: 7.00am - 19.00pm
Sunday: 8.30am - 19.30pm
x

We always support in emergencies, contact us immediately if you are experiencing any serious health problems.

Contact With Us!

Address: 4425 Fremont California USA

Support mail: contact@zaifitech.com

Opening Hours: Mon -Sat: 7.00am – 19.00pm

USA +1 – 2093219310
India +91-7330812365