Drug Development Services Malaysia

We leverage our experience to share unique perspectives and ultimately deliver your results. Partner with our Malaysian team to access solutions from our neighboring operational units and global resources.

• Nonclinical Development: Our dedicated CFDA GLP certified facility in Shanghai, China features a number of accreditations to fulfill global quality standards (FDA, OECD, etc.). Teaming up with Covance global resources and partners in China, we offer solutions for a full range of safety assessments needed by IND filing and FIH. Specific solutions for small molecules and biologics include:
  • Lead Optimization
  • Safety Assessment
  • Bioanalysis
  • Drug Metabolism and Pharmacokinetics
  • Chemistry, Manufacturing and Controls
• Clinical Testing - Central Laboratory Services: Trust in the experience of the Singapore central lab to deliver consistent, quality data and on-time data transfers for faster submissions. Operating since 2000, we offer one of the biggest central laboratories in the world, serving 16 countries in the Asia Pacific region.
  • Core Laboratory Testingservices:
    • Genomics Services
    • Special Chemistry
    • Immunochemistry
    • Hematology
    • Flow Cytometry
    • Specimen Management and Biorepository
    • Safety Testing
  • Anatomic Pathology
  • Biomarker Services
  • Scientific Consultation
  • Data Management
  • Project Management
  • 调查员网站增刊ort
  • Global Logistics
• Clinical Trial Support:Improve operational efficiencies and accelerate your timeline with our streamlined start-up process.
  • Early Clinical/Phase IIa
    • Clinical Pharmacology
    • Early Patient Studies
    • Clinical Trial Project Management and Monitoring
    • Complete PoC^®
  • Phase IIb/III
    • Xcellerate^®Clinical Trial Optimization^®
    • Clinical Trial Management
    • Xcellerate^®Monitoring
    • Drug Safety
    • Functional Service Provider
  • Life Cycle Management
  • Clinical Data Analysis and Reporting
  • Regulatory

Ensure your locally-based and large-scale global studies meet international standards with help from our local scientific experts.

• Regulatory expertise: Get experienced consulting with your regulatory submissions from our regional team of experts.
• Site monitoring: Ensure patient safety, data quality and your study’s integrity with our holistic site monitoring solutions.
• Project management: Receive expert guidance through any phase of your clinical trial by working alongside our dedicated project managers.

While Malaysia is still an emerging area for clinical trial activity, recent government support suggests a future increase in clinical research sites. Other considerations include:

• Integrated resources: The government continues to develop a comprehensive network of its healthcare facilities and form partnerships with private hospitals.
• Attractive patient pool: A large and diverse multi-ethnic population comprises an attractive patient base for clinical trials.

With our unique combination of regional knowledge and global experience, we’re ready to work together and explore what’s possible. Learn more about how we can deliver your results.