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UID:2140535:Event:63351
DTSTAMP:20260509T203041Z
SUMMARY:Cosmetics - How Are they Regulated?
DESCRIPTION:This webinar will provide a comprehensive overview of FDA 
 regulations for cosmetic products. It will help you understand how to 
 be compliant in manufacturing, labeling and advertising of cosmetic pr
 oducts, and thereby ensure successful FDA and state inspections.\n\nWh
 y Should You Attend:\nBeing unaware of the regulations that apply to t
 he cosmetics industry is a tenuous position to be in. Should your prod
 ucts come under scrutiny, will you be able to pass FDA and state inspe
 ctions or will your business be in jeopardy?\nThis presentation will h
 elp the management and staff of cosmetics companies to understand the 
 regulations and how they apply to their products. It will help attende
 es gain a strong understanding of what is involved in becoming complia
 nt in manufacturing, labeling and advertising of cosmetic products. At
 tendees will learn the importance of documenting and following up on c
 onsumer complaints, the marketing errors to avoid, the value of tracki
 ng lots, maintaining retention samples, having a quarantine area and i
 ts purpose, the necessity in using good manufacturing practices (GMP) 
 in the manufacturing of cosmetics and the possibility of needing a qua
 lity testing program.\nWhether you are a contract manufacturer or make
  your own products, compliance with GMPs will ensure quality productio
 n, and minimize corporate risk. Safeguarding consumer health is a key 
 priority. Compliance will also ensure successful FDA and state inspect
 ions. This session will include the key principles of GMP as defined b
 y FDA as well as incorporate FDA regulatory inspection strategy to ide
 ntify areas of common deficiency.\nAreas Covered in the Webinar:\n\nDi
 fferences between drugs and cosmetics.\nGood Manufacturing Practice (G
 MP).\nRole of quality Assurance in the manufacturing process.\nRespons
 ibilities of management in FDA compliance.\nImportance of a good produ
 ct surveillance program.\nEducation of employees on GMPs and complaint
  handling.\nActivities that are common to manufacturing processes.\nLi
 nking responsibility to these activities.\nState Health Departments an
 d their relationship with FDA.\nCase study on the manufacture of a cos
 metic from raw materials to sale.\n\nWho Will Benefit:\nThis webinar w
 ill provide valuable assistance to the following personnel:\n\nBusines
 s owners\nManagers in manufacturing and customer service\nNew staff in
  manufacturing\nQuality Assurance\nAdministrative managers in charge o
 f operations\nRegulatory Compliance Associates and Managers\n\nInstruc
 tor Profile:\nSusan Augello-Vaisey,M.S. is the owner and Senior Consul
 tant at Pharma Consulting Solutions, LLC. She is a consultant in the c
 osmetic and pharmaceutical industry and is the author and presenter of
  multiple GMP and GCP compliance related courses and programs. She has
  successfully led small cosmetic firms through the metamorphosis from 
 total non-compliance with imminent shut-down through system developmen
 t and company education to regulatory compliance. These changes result
 ed in improved company compliance and increased market value.\n\nFor m
 ore information visit https://medtechiq.ning.com/events/cosmetics-how-
 are-they-regulated
DTSTART;TZID=America/New_York:20140312T100000
DTEND;TZID=America/New_York:20140312T110000
CATEGORIES:pharmaceutical
LOCATION:Online Event
WEBSITE:http://www.complianceonline.com/ecommerce/control/trainingFocu
 s/~product_id=702311?channel=medtechiq
URL:http://www.complianceonline.com/ecommerce/control/trainingFocus/~p
 roduct_id=702311?channel=medtechiq
CONTACT:+1-650-620-3915
ORGANIZER;CN=ComplianceOnline:https://medtechiq.ning.com/profile/Refer
 ral512
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562006613?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
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