CAPA Documentation and Filing Tackling the Least Understood Parts of the Process

Held Jan. 31, 2013

You could have the world’s greatest surveillance network to alert you to CAPA problems, your failure investigation teams could be top-notch, but if you fail to write clear and concise reports, include the right level of documentation and file these CAPAs so they’re easily handed to the FDA during an inspection, you’ve failed.

On Thursday, Jan. 31, 2013, FDAnews presented four back-to-back sessions dedicated to CAPA documentation and filing.  No other event in the industry has tackled this complex subject like this.

Order Today

A top-notch investigation is no good if your report is not clear and concise enough to pass FDA scrutiny. Would your CAPA documentation pass FDA scrutiny?

You will master CAPA documentation and filing compliance in just one day.  Here’s how.

You’ll hear from four experts on FDA documentation regulations, filing systems, report preparation, and best practices for correcting mistakes.  You’ll come away knowing how to transform your CAPA documentation and filing problems into successes.

Get answers to your toughest documentation questions — in just a day.  No travel required.  Gather your colleagues for the best, and most cost effective, training in the industry.

Order your CD/Transcript of CAPA Documentation and Filing: Tackling the Least Understood Parts of the Process today.

  • CAPA mangers
  • QA/QC managers and directors
  • Compliance officers
  • Training managers
  • GCP, GLP or GMP professionals
  • Regulatory affairs managers
  • Quality engineers

Phone: toll free (888) 838-5578 (inside the U.S.) or +1 (703) 538-7600