Trending FDA 483 Report Sample

Do NOT wait for the FDA to come a-knocking!

Pharmaceutical manufacturers often wait until after an FDA inspection to invest in quality assurance and regulatory compliance systems. However, investing in GMP Trends has proven to reduce 483’s and improve quality structures. Receiving an FDA 483 warning letter could lead to a shut down of a pharmaceutical manufacturing facility, and the resulting loss of production would have an extremely negative financial impact.

GMP in the pharmaceutical industry, or Good Manufacturing Practices, is nothing to be taken lightly. Learn from the mistakes of other manufacturers – Take a proactive approach to your quality systems and be prepared for your next inspection to prevent FDA 483 warning letters. Download a sample 483 report below to learn how GMP Trends can help you stay compliant withe FDA.

Get access to our Biweekly Trending 483 Report.

GMP Trends is an FDA Compliance Platform, providing relevant, real-time, and unbiased information reports trending USFDA 483-inspection observations. Our team understands the dynamic between the operational executives and the quality assurance teams, because we’e been there. Read the GMP Trends Report today, and leverage your efforts to safeguard product quality.

For over 40 years, GMP Trends has served as a regulatory intelligence resource for quality assurance, regulatory compliance, and R&D professionals in the pharmaceutical and medical device industries. GMP Trends’ Reports will help you formulate quality strategies, learn from the mistakes of other firms, and best prepare for stressful and tedious FDA inspections.

Sample Biweekly Trends Report delivered to your inbox!

The twice-monthly GMP Trends report contains curated 483-observations, delivering only the essential information to keep you in compliance and up to date on the most recent actions of the FDA. Regain your Confidence In Compliance with GMP Trends and download a sample biweekly GMP Trending 483 Report from today.

Get access to our Biweekly Trending 483 Report.

Become A Subscriber And Stay Ahead of the FDA

To get the most out of GMP Trends®, sign up to one of our subscription packages for valuable, up-to-date information you won't find anywhere else! Every subscription provides the most frequently cited FDA 483 observations taken from recent FDA Inspections. The non-essential information is redacted to streamline the facts in an easily readable format. Join the thousands of professionals who rely on GMP Trends® to keep them informed of the latest FDA Enforcement Trends!