Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Advertising

Event Details

Filter
WorldWebinar

Dietary Supplements CGMPS - 21 CFR 111 Compliance


Add this event to your calendar: iCal   Google Calendar

Who should attend?

Senior Management in Dietary Supplements Industry QA/RA R&D Engineering Marketing Consultants Others Tasked with Product, Process, Validations, CGMP Responsibilities Interested Consumer Groups Medical and Other Healthcare Professionals, Staff and Office Personnel Start-Ups

Details

Overview

21 CFR part 111 ("the DS CGMP rule") requires persons who manufacture, package, label, or hold a dietary supplement to establish and follow current good manufacturing practice-the CGMPs. This is to ensure the quality of the dietary supplement and to ensure that the dietary supplement is packaged and labeled as specified in the master manufacturing record.

This webinar will discuss basic Dietary Supplement CGMP of Part 111 and related requirements, to include:

Quality Management System / QA / QC

Personnel, Facilities, Equipment

Software controls

Production and Process Controls

Holding and Distribution

Complaints and Returns

Records

Why should you Attend

FDA regulates dietary supplements under a different set of regulations than those covering "conventional" foods and drug products. Under the Dietary Supplement Health and Education Act of 1994 (DSHEA), Congress defined the term "dietary supplement", and requires that every supplement be labeled a dietary supplement. Beyond that, the industry was only subject to voluntary quality management systems and controls / GMPs, until the Dietary Supplements CGMPs were published as a "final rule" by the FDA, 21 CFR 111, in 2007.

Failure to follow these requirements results in products being termed "adulterated" or "misbranded" by the Agency. There is confusion in the industry as just what type of manufacturing controls and record keeping, and labeling content is required by the FDA, and this confusion continues to cause regulatory problems for many new and established companies in this industry.

Areas Covered in the Session

History of Dietary Supplement regulation in the U.S

The Dietary Supplement Health and Education Act (DSHEA)

The key requirements of the Dietary Supplements CGMPs, 21 CFR 111

Required steps for CGMP compliance

Problem areas, common pitfalls

Implementation: Systems, templates and tools

Prices

$150

Contact

Joseph Wilcox
traininngdotcom@gmail.com

Advertising
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.