BioPharm-Medicine.com
  • Home
    • About Us
    • Stories >
      • Bernadette's Story
      • Sharyn's Story
  • Roles
    • Executive Positions
    • Pharmacology/Toxicology
    • Clinical Research
    • Biostatistics
    • Data Management
    • Regulatory Affairs
    • Medical Writing
    • Medical Affairs
    • Clin. Res. Organizations (CROs)
    • Consultants & Contractors
  • Teamwork
    • Investigator's Brochure
    • Clinical Study Reports
    • Filing an NDA
    • Promotional Review Committee
  • Training
    • Common Abbreviations
    • Canadian HPFB
    • Clinical Reseach >
      • Clinical Study Reports
      • Draft PI
      • Investigator's Brochure
      • Phases of Clinical Development
    • Discovery/Design >
      • Toxicology
      • PharmacologyPK
    • The FDA >
      • The IND
      • The NDA
      • The PI
    • European Regulations
    • Safety/Pharmacovigilance
  • Resources
    • CME
    • European Agencies
    • FDA websites & Org Charts
    • Guidance Docs and Guidelines
    • Professional Organizations
    • Other Links
  • Protocol Writing


​TRAINING

​

Short courses
​
CME

The pages in this sections will provide information

​about a wide variety of topics including about:


 
 Abbreviations commonly used in industry,

 The FDA and International Regulatory Organizations

 Training programs

  Continuing Medical Education

​  Clinical Research

    Draft Package Insert

    Investigator's Brochures

    Phases of Clinical Research

Drug Discovery

    Toxicology
    
     Pharmacology


​