Tag Archives: FDA Form-483

Sizing up the Dark Side: An overview of the NBJ Dark Issue

Date/Time: March 30, 2016, 2:00pm ET / 12:00 MT

Cost: $95

Description:

The Dark Issue is the most talked about issue in NBJ history and we’re ready to talk about it some more. Join us March 30 at 2 p.m. eastern standard time for a webinar examining some of the biggest challenges facing the supplement industry. Topics to be discussed include:

  • Adulteration in the supply chain
  • Best use of scientific studies
  • Spiking in sports medicine
  • GMP violations and FDA Warning Letters
  • Retailers as gatekeepers
  • What the industry is doing to hold onto consumer trust
  • What a new approach to regulation could mean

The first quarterly webinar of 2016 will feature presentations and discussion with:

Steve Mister
President
Council for Responsible
Nutrition
Todd Harrison
Supplements Lawyer
Risa Schulman
Science Consultant
Tap~Root
Marian Boardley
GMP Specialist

Bring questions!

The presentations will be followed by what we expect to be a lively Q&A. The Dark Issue webinar is free to subscribers, or with a purchase of the Black Issue Extended Edition. Or buy a seat for $95.

FY2015: Dietary Supplement cGMPs – FDA Inspection Observations

FDA released new spreadsheets for FY 2015 (10/1/2014 – 9/30/2015) which have now been incorporated into my charts.

BySubpart-cGMP-21CFR111

The total number of observations found during cGMP inspections at dietary supplement firms has declined from FY 2014 (the peak was in FY 2013). Production and Process Control (Subpart E) citations continue to dominate, consisting of ~30% of the problems found. In FY 2015, finished product specifications for identity, purity, strength, composition (and for limits on contaminants) remained the most frequent item (as it was in FY 2014) but by a greater margin. Identity testing of components, followed by batch record requirements, continue to top the list of inspectors’ favorite inspection findings.

FDA releases updated Inspection Classifications for FY 2015

FY2015-1

For those of you who track this stuff, FDA just released new inspections classifications data that can be found at: http://www.fda.gov/ICECI/Inspections/ucm222557.htm

The above chart shows FY2015 inspection classifications in all CFSAN project areas (foods, cosmetics, dietary supplements) and their outcomes  (OAI – Official Action Indicated; VAI – Voluntary Action Indicated; NAI – No Action Indicated)  OAI and VAI means that a 483 was issued in a particular project area, NAI means basically a clean inspection.

FDA: Preliminary FY 2015 483 Data at Rocky Mountain DS Forum

Based on preliminary FY 2015 data released by FDA’s Denver District at the Rocky Mountain Dietary Supplement Forum in Boulder, Colo. last week, Form-483 citations are down overall for dietary supplement firms, and there has been a shift from focusing on identity testing of ingredients (although this is still a very common and important finding) toward observations related to setting specifications for finished products.  This trend continues from FY 2014.  Data are preliminary because FY 2015 was not yet closed when the data were gathered (closes Sept 30, 2015).  I will be publishing complete FY 2015 figures when they become available from FDA’s website.  In the meantime, here is a chart based on last week’s data and historical 483 observations from 2009-2014, ordering is based on preliminary FY 2015 frequency.

FY 2015 Form 483 preliminary

Note: there are a total of 11 CFR sections listed above (as presented by FDA representatives)

Webinar: FDA Inspections & Emerging cGMP Compliance Issues for Dietary Supplements

The American Herbal Products Association (AHPA) will present a two-hour educational webinar titled “FDA Inspections & Emerging cGMP Compliance Issues for Dietary Supplements – Recent 483s,” on Thursday, October 1, 2015, from 1:00-3:00p.m. ET.
A regularly occurring event and part of the association’s cGMP Compliance Series, this two-hour, webinar is designed to help those businesses in the dietary supplement industry understand the elements of 21 CFR 111/current Good Manufacturing Practices (cGMP) regulations that are most focused on during recent FDA inspections. This knowledge will assist business with better allocating their compliance resources.
Veteran industry legal experts will provide attendees with an insider’s view of current cGMP enforcement landscape. AHPA staff will offer a detailed analysis of the association’s repository of inspection data, widely regarded as the most in-depth in the industry and which includes actual FDA 483 Inspection reports, Observation forms, and establishment inspection reports (EIRs).
Topics:
  • What aspects of the cGMP are you responsible for during an inspection?
  • FDA “Hot buttons” during inspections and what can be done to prepare as well as mitigate
  • Detailed analysis of recent (2014-present) FDA inspection reports
  • What the inspection reports teach and how to appropriately respond to a Form FDA 483
  • Answers to your questions during the Q&A session
Presenters:
  • Tony Young, Kleinfeld, Kaplan & Becker/AHPA General Counsel
  • Marian Boardley, Marian Boardley Consulting, LLC
  • Merle Zimmermann, Ph.D., AHPA
Moderator:
  • Jane Wilson, AHPA
A 20-30 minute Q&A session will follow the speaker’s presentations to allow attendees to anonymously ask specific questions about FDA inspections, enforcement actions, and related matters.