ANDA Submission and GDUFA Guidance

  • 329.00 Dollar US$
  • Published date: September 22, 2020
    • Palo Alto, California, United States

In order to properly, effectively, and efficiently bring generic drugs and medicinal products to market, it is crucial to anyone interacting with the submittal process to understand how the process is structured and functions

Result 0 votes
Ashutos Swain
0 votes

Useful information

  • Avoid scams by acting locally or paying with PayPal
  • Never pay with Western Union, Moneygram or other anonymous payment services
  • Don't buy or sell outside of your country. Don't accept cashier cheques from outside your country
  • This site is never involved in any transaction, and does not handle payments, shipping, guarantee transactions, provide escrow services, or offer "buyer protection" or "seller certification"

Related listings

  • Medical Claims Boot Camp

    Medical Claims Boot Camp

    Drug Development Fremont (California) August 7, 2020 545.00 Dollar US$

    This course covers the fundamentals of medical billing, coding, and reimbursement by explaining how all of these components work together. Emphasis will be placed on the practical application of the latest industry knowledge and standards, with the g...

  • Fraud & Abuse, Stark & Anti-Kickback Issues

    Fraud & Abuse, Stark & Anti-Kickback Issues

    Drug Development Fremont (California) December 4, 2019 139.00 Dollar US$

    Overview: The presentation will provide an overview of the Federal Stark and Anti-Kickback laws and corresponding regulations including the history and purpose of these laws. The presenter will provide the background upon which these laws were determ...

  • 6-Hour Virtual Seminar on Batch Record Review and Product Release

    6-Hour Virtual Seminar on Batch Record Review and Product Release

    Drug Development Fremont (California) July 3, 2019 545.00 Dollar US$

    Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records. Additionally, there must be written procedures for a batch record review process that demonstrate c...