Regulatory Training and Education Programs

Improve your internal product development capabilities by gaining knowledge and resources from our experienced consultants

Regulatory workshops

The primary objective of our customized regulatory workshops is to share opportunities for you to benefit from our scientific and regulatory expertise. Our expertise has been gained from four decades of hands-on interactions with the FDA and global regulatory agencies to prepare and submit regulatory documents. You will gain the knowledge needed to  improve your internal capabilities and maintain approvals throughout the entire product lifecycle.

The four workshops we most often provide are:

  • U.S. Pharmaceutical Development and Regulatory Systems
  • Quality and Current Good Manufacturing Practices (CGMP) Workshop:  U.S. General Regulatory Systems and CGMP
  • Scientific and Regulatory Affairs Workshop:  U.S. General Regulatory Systems and Investigational New Drug (IND) Application
  • Scientific and Regulatory Affairs Workshop:  U.S. General Regulatory Systems and New Drug Application (NDA)

Cardinal Health will work with you to build a customized workshop that is deisgned to meet the needs of your team.

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Learn how we can help guide your product to regulatory approval.

913.451.3955
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