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    • eCTD Guidance & Submission
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Our Services

At BioPharma Global, we take pride in offering unparalleled expertise that meets your needs in variety of service offerings with competitive pricing that won’t stretch you budget.

  • FDA and EMA Regulatory Affairs Submissions 
  • FDA and EMA Regulatory Strategy Development
  • Medical Devices and Combination Products Services
  • FDA Orphan Drug Designation (OOD)
  • Investigational New Drug Application (IND)
  • Fast Track Designation
  • Breakthrough Therapy Designation
  • Electronic Common Technical Document (eCTD)
  • Rare Pediatric Disease Designation (RPDD)
Biopharma Global - FDA & EMA Regulatory Affairs Consulting Services
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