ChemPharm
超越合规
ChemPharm 专注于亚洲市场，拥有不断扩展的专业知识，在法规事务、合规、验证、培训和灵活资源配置方面提供无与伦比的咨询服务。
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
我 们的独特之处是什么？
经验丰富的团队
我们的高级顾问均拥有超过 30 年的专业经验，并与 FDA 直接合作，此外还有专门的顾问提供支持。
敏捷且个性化的服务
我们提供敏捷的响应速度和及时的服务保证，通过个性化的关注和量身定制的方法，优先考虑客户的需求。
行业认可的解决方案
我们提供高效、经济的解决方案，并拥有业内认可度和广泛的人脉网络作为后盾。
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.”
