Beyond Compliance
Specialising in the Asia market with expanding expertise, ChemPharm provides unparalleled consulting in Regulatory Affairs, Compliance, Validation, Training and Flexible Resourcing.
Our Services
Comprehensive regulatory and compliance support from first gap assessment to full audit readiness for pharma, biotech, medical device, and TCM companies across Asia.
Compliance
Gap analyses, QMS development, and GMP/GDP/GLP/GCP compliance, backed by independent audits.
Regulatory Affairs
Regulatory guidance from product development through submission, ensuring compliant market entry.
Validation
Process, equipment, facility, and software validation — from strategy through documentation.
Training
GMP, QSR, GDP, and GLP training that prepares your team for FDA inspections.
Flexible Resourcing
Remote or on-site expert support, scaled to your project's exact needs.
Global Presence
Singapore
From our base in Singapore, ChemPharm has grown to support clients across Asia — with new markets on the horizon.
China
Hong Kong
Japan
Vietnam
Malaysia
Our Edge
Experienced Team
Our senior consultants each bring over 30 years of expertise and direct collaboration with FDA, supported by additional dedicated consultants.
Agile & Personalised Service
We offer agile responsiveness and guaranteed timely service, prioritising client needs through personalised attention and a tailored approach.
Industry Recognised Solutions
We provide efficient, cost-effective solutions backed by our industry recognition and extensive network of relationships.
Client Success Stories
100+
“The methodical approach and strategic growth insights have been provided to over 100 customers since the inception of Chempharm."
30+
“With over 30 years of combined pharmaceutical expertise, we have successfully guided our clients through complex regulatory and market challenges.”
40%
“We achieved a 40% increase in strategic growth within a single year through Chempharm's expert consulting and methodical industry expertise.”
