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Strategies To Prevent Manufacture And Distribution Of Substandard Medications

 
  February 25, 2019  
     
 
Netzealous LLC DBA - Compliance4All, Online
2019-04-10


Overview:
In this webinar we will provide you with best practices that have been proven effective, and equip you with the means to advocate for these ideas within your organization.

Why should you Attend:
If a legitimate product is not manufactured according to quality standards or becomes degraded as it travels through its supply chain, it can be ineffective at best or deadly at worst. Examples of potential dangers that can occur include temperature excursions, inappropriate use, and unsafe ingredients inadvertently added to the product.

Areas Covered in the Session:
Solutions
Maintain a robust quality system
Supplier quality
Product testing
Monitoring temperature

Who Will Benefit:
Pharmaceutical Industry
Supply Chain
Quality Assurance
Packaging and Labeling
Manufacturing
Warehousing and Distribution

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14@gmail.com
 
 
Organized by: Event Manager
Invited Speakers:
Speaker Profile:
Michael Esposito has over 30 years experience in the pharmaceutical industry and 17 years experience in GMP training and document management. He has worked for Wyeth Pharmaceuticals, Pfizer and Johnson & Johnson's McNeil Consumer Healthcare Division in a variety of areas including Packaging, project administration, Quality Assurance, Government Contracts, translations, systems training, and international operations.
 
Deadline for Abstracts: 2019-04-08
 
Registration: https://www.compliance4all.com/control/w_product/~product_id=502381LIVE?channel=hum-molgen_Apr_2019_SEO
E-mail: compliance4all14@gmail.com
 
 
   
 
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