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
Therapeutic Brochures

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.

 

 


Company Overview   |   Services  |  Operations   |   Case Studies   |   Careers  |  Investigators  |   Contact

© 1994 - 2009 Pharm-Olam International. All Rights Reserved.