Core Expertise

Training
Comprehensive training across GMP, GDocP, QMS, CSV, QRM, Cleaning Validation, and Schedule M compliance, delivered on-site, virtually, or as customized workshops for teams at every level.


Validation
End-to-end validation across computer systems, cleaning processes, and facilities, ensuring product quality and regulatory compliance at every stage of manufacturing.
Expert regulatory audits and risk assessments to ensure full compliance with Schedule M, WHO, US FDA, EMA, ICH, and other international GxP standards — safeguarding operational integrity across your operations.
GMP Auditing

Engineered for Compliance
We bridge the gap between complex regulatory frameworks and operational excellence. Our approach integrates clinical precision with rigorous quality risk management, ensuring your pharmaceutical processes meet the highest industry standards for safety and efficacy.
COMMITMENT
Advanced Consulting for the Life Sciences
ComplianceCompassPharma was founded on the principle that precision is the cornerstone of pharmaceutical excellence. We provide a clinical approach to GxP consulting, ensuring that every regulatory interaction and quality risk management decision is backed by rigorous data and a deep understanding of the global regulatory landscape.

Testimonials

"Understanding how US FDA auditors actually think changed how our team prepares documentation."
Vaibhav Saswadkar
Assistant Manager, Top Pharma MNC

"Our documentation review process improved noticeably. I'd recommend this training without hesitation."
Gourav Naik
QMS officer at Markson Pharma Pvt. Ltd

"Breaking down ALCOA++ against our actual batch records helped us spot gaps we hadn't noticed in years."
Sonali Patil
Executive Production(MES) at Encube Ethicals Ltd, Goa

"We came away with a much sharper eye for spotting gaps before an external auditor does.An excellent choice for any organization serious about closing gaps before the next inspection."
Anil Panigrahi
Assistant Manager at Sanofi, Goa
GxP COMPLIANCE • GMP AUDITING • VALIDATION • REGULATORY AFFAIRS
