Pharm-Olam provides first class services to support your needs in the clinical trial process.

• Rapid Patient Recruitment
• Monitoring
• Regulatory and Ethics Submissions
• Data Management
• Biostatistics
• Project Management
• Pharmacovigilance
• Import/Export Licenses
• Contract Negotiation and Administration
• Product Registration
• Feasibility Studies
• Protocol Design
• Investigator Identification
• DSMB Management
• Quality Control/Assurance
• Medical Writing
• CTMS
• Translations
• Case Report Form Design
• Investigator Meetings & Staff Training
• Toxicology Studies

Do you need a Regulatory or Biostatistics consultant? Our experts can assist you with all your development and commercialization needs on a local or global scale. They can diagnose and tailor solutions to your needs, from pre-clinical through the life of your product to maximize value, regulatory compliance, and quality.