Accreditation

 

Potential objectives:

  1. To provide participants with a foundational understanding of the relevant literature, policies, and laws surrounding pharmaceuticals in the era of corporate science
  2. To equip participants with the knowledge and skills required to understand and assess regulatory documents, address reporting biases, and evaluate regulatory sources
  3. To inform participants of the legal and ethical context surrounding clinical trial data transparency; including: the changing regulatory environment, the comparison of pharmaceutical regulation models across jurisdictions, and conflicts of interest
  4. To provide participants with a broader understanding of the social and political context surrounding clinical trial data transparency

Accreditation

TBD