Recent FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies

Added by Referral on 2018-06-15

Conference Dates:

Start Date Start Date: 2018-09-26
Last Date Last Day: 2018-09-26
Deadline for abstracts/proposals Deadline for abstracts/proposals: 2018-09-25

Conference Contact Info:

Contact Person Contact Person: Ashutos Swain
Email Email: [email protected]
Address Address: online event, Palo Alto, United States

Conference Description:

This training program will provide attendees with a better understanding of the current audit techniques used by FDA and how they have changed over the years. In addition, areas of increased regulatory scrutiny will also be discussed such as data integrity issues. Additionally, the webinar will provide an overview that companies can use to evaluate their own state of compliance by knowing what have been the most common cited GMP deficiencies over the last several years.
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