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Services

Regulatory Affairs

Regulatory Affairs

Our multi-lingual regulatory professionals assist you to prepare comprehensive regulatory dossiers and guide you through the complexities of regulatory affairs across Asian countries with effective strategies and solutions to ensure your project progresses as planned

  • Study Dossiers Preparation
  • IRB/Regulatory Authority Submission
  • Supplies Importation and Exportation
  • Pharmaceutical Product and Medical Device Registration
Site Management

Site Management

Our experiences and efficiencies in managing clinical trials with all sizes, cross-countries, complexities and diverse therapeutic areas add value to recruitment and retention processes to enable you to achieve or even shorten study enrollment timelines

  • Site Coordination
  • Subject/Patient Recruitment
  • Subject/Patient Registration
  • Clinical Supplies Management
Clinical Trial Management

Clinical Trial Management

Our high caliber project management and clinical monitoring team provide efficient and quality deliverables exceeding your expectations

  • Feasibility Study
  • Site and Investigator Selection
  • Clinical Project Management
  • Clinical Trial Monitoring
  • GCP and Quality Auditing
  • Safety and Pharmacovigilance
Biometrics

Biometrics

Our diligent biometric professionals deliver accurate data analysis, reporting and high-quality output to ensure on-time and on-cost deliverables

  • Protocol Development
  • CRF and e-CRF Development
  • Data Management
  • Statistical Analysis
  • Medical Writing
  • Study Drug Allocation
Consulting

Consulting

Our reputable consultants provide in-depth guidance and advice to meet your needs ranging from regulatory affairs, product/medical device development, to medical and healthcare market intelligence

  • Regulatory Affairs
  • Product Development Support
  • Medical Device Development
  • Medical and Healthcare Market Research