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  Regulatory Affairs

  Accelerated Registration Pathways in USA and Canada for Pharmaceuticals

  $499.00 Add to cart
• 
  Pharmacovigilance

  Benefit-Risk assessment in Pharmacovigilance

  $499.00 Add to cart
• 
  Clinical Research

  Bio-Ethics, Legislations and International Guidelines

  $299.00 Add to cart
• 
  Inspections and Audits

  Chemistry, Manufacturing, and Controls (CMC) for Drug Submissions

  $499.00 Add to cart
• 
  Clinical Research

  Clinical Project Management

  $499.00 Add to cart
• 
  Uncategorized

  Clinical Research Management and Data Analysis

  $499.00 Add to cart
• 
  Uncategorized

  Clinical Research Management and ICH-GCP

  $850.00 Add to cart
• 
  Uncategorized

  Experiential Learning Internship – Preparation of an NDA in CTD format for FDA (8 weeks)

  $499.00 Add to cart
• 
  Uncategorized

  Experiential Learning Internship – Preparation of an NDA in CTD format for FDA (8 weeks)

  $499.00 Add to cart
• 
  Uncategorized

  Experiential Learning Internship – Preparation of an NDA in CTD format for FDA (8 weeks)

  $499.00 Add to cart
• 
  Uncategorized

  Experiential Learning Internship – Preparation of an NDS in CTD format for Health Canada (8 weeks)

  $499.00 Add to cart
• 
  Regulatory Affairs

  FDA’s accelerated approval process for new medicinal products

  $399.00 Add to cart