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

Quantity Discounts
1 - 9999
1 - 9999
1 - 9999
1 - 9999
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.

FDAnews presents four back-to-back sessions dedicated to CAPA documentation and filing.  No other event in the industry has tackled this complex subject like this.

Register 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?

If you’re unsure, listen in today.

You’re going to 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 from this virtual conference encore presentation 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.

Register Today

Everyone in your organization with a role in product development, legal and regulatory affairs will benefit from taking part in this event — and they can do so at a cost that won’t break the budget. You pay a single low registration fee per facility, regardless of how many participate. So spread the word.

Sign up for CAPA Documentation and Filing: Tackling the Least Understood Parts of the Process today.

Here’s How It Works

Attendees will receive all presentations after registering.

Then, just log on to the encore presentation website provided in your registration confirmation and relax. That’s all there is to it.

Don’t take unnecessary risks.

Sign up now

  • CAPA mangers
  • QA/QC managers and directors
  • Compliance officers
  • Training managers
  • GCP, GLP or GMP professionals
  • Regulatory affairs managers
  • Quality engineers
Date: Feb. 4–22, 2013
Location: Your office or conference room (no need to travel!)
Time: Anytime

Send Your Team for Maximum Benefit
Get your team up to speed!

Significant tuition discounts are available for teams of three or
more from the same company. You must register at the same time and
provide a single payment to take advantage of the discount. Register below
by clicking on add to cart and then change your quantity in the shopping cart.
The discount will be calculated automatically.

3-4 attendees – 10%
7-9 attendees – 20%
5-6 attendees – 15%
10+ attendees – 25%

Call (888) 838-5578 in the U.S. or +1 (703) 538-7600
globally with any questions.

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Or, register by phone: toll free (888) 838-5578 (inside the U.S.) or +1 (703) 538-7600

Registrations may not be cancelled. Please contact Customer Service to make any substitutions.