Our Compliance Expertise
Our Main Services
Worldwide GxP auditing — internal audits, supplier audits, remote audits, gap analysis, training, and consulting.
Learn MoreOur Facilities
Each assignment is managed by a dedicated project manager acting as your single point of contact (SPOC).
Learn MoreOur Location
Plot No. 64, 5th Floor, Arunachal Classic, KBHP 6th Phase, Kukatpally, Hyderabad, Telangana – 500085.
Learn MoreRequest an Audit
When quality issues arise, we respond swiftly to assist our GxP clients worldwide. Contact us today.
Learn MoreLatest Pharmaceutical Audit Technology & Expertise
Our auditors are seasoned GxP professionals with extensive regulatory knowledge. We offer cost-effective audit partnerships with a solution-oriented approach, serving pharmaceutical companies across the globe.
Excellence
Focused
Our Expertise
Impeccable pharmaceutical audit services tailored to your compliance needs.
GCP Audit & Monitoring
Comprehensive GCP auditing — project management, bioanalytical monitoring, and clinical phase monitoring.
View DetailsGMP Audits
GMP audits covering qualification, compliance & upgradation audits, and full GMP consulting services.
View DetailsGLP Audits
GLP audits including facility qualification, GAP analysis, study protocol/report audits, and process audits.
View DetailsQMS Consulting
Quality Management System consulting — compliance plans, QMS frameworks, and continuous monitoring.
View DetailsRegulatory Affairs
End-to-end regulatory strategy, dossier submission, eCTD publishing, and product lifecycle management.
View DetailsGxP Training
Professional GxP training programs — GMP, GCP, GLP, Data Integrity, and Auditor Qualification.
View DetailsNumbers That Speak For Themselves
Trust Us
Why People Trust Kandula Pharmavigilence
Trusted by pharmaceutical companies worldwide for our expertise, precision, and responsiveness.
Deep Knowledge
Extensive expertise in GCP, GMP, and GLP regulatory requirements across global markets.
Proven Experience
Seasoned auditors with extensive GxP experience across global pharmaceutical markets.
Rapid Response
When quality issues arise, we respond swiftly to assist our GxP clients worldwide without delay.
Exceptional Value
Highly competent auditors delivering precise results promptly at competitive, transparent cost.
Industries We Serve
Pharmaceutical Manufacturers
GMP qualification, compliance upgradation, and plant setup consulting for drug manufacturers.
Contract Research Organisations
GCP audits, clinical monitoring, and CRO/site identification for clinical trial organisations.
Research & Analytical Labs
GLP facility qualification, GAP analysis, and 21 CFR Part 58 compliance audits for labs.
Biotech & Biopharmaceutical
Regulatory strategy, eCTD dossier preparation, and lifecycle management for biotech companies.
Clinical Trial Sites
Site qualification audits, for-cause investigations, and regulatory compliance for clinical sites.
Global Market Entrants
Country-specific regulatory support for companies entering regulated and ROW markets worldwide.
What Our Clients Say
Kandula Pharmavigilence's GCP audit team was thorough, professional, and responsive. Their dedicated project manager made the entire process seamless.
Their GMP auditors helped us identify critical gaps and implement solutions that brought our facility into full regulatory compliance. Exceptional service.
Outstanding GLP audit service. Their expertise in 21 CFR Part 58 compliance saved us significant time and resources. Highly recommended.
