Packaging and Labeling in Pharmaceutical Product Development – Best Practices

Posted By : User Ref No: WURUR44656 0
  • Image
  • TypeWebinar
  • Image
  • Location Newark, Delaware, United States
  • Price
  • Date 17-10-2019
Packaging and Labeling in Pharmaceutical Product Development – Best Practices, Newark, Delaware, United States
Webinar Title
Packaging and Labeling in Pharmaceutical Product Development – Best Practices
Event Type
Webinar
Webinar Date
17-10-2019
Last Date for Applying
17-10-2019
Location
Newark, Delaware, United States
Organize and Presented By
247compliance
Sponsored By
247compliance
Organizing/Related Departments
Food and Drug Administration
Organization Type
Event Organizing Company
WebinarCategory
Non Technical
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Food Processing

Location
Newark, Delaware, United States
  • OVERVIEW

Occupying a critical position in the success or failure of any pharmaceutical product launch, Packaging and Labeling form a bridge between the conception of a product and its realization and distribution. Their activities are also crucial for compliance with regulatory agency requirements.
Still, their importance is often underestimated, especially in the planning phases, which leads to unnecessary increases in cycle time, costly errors, delays in product availability, or product recalls due to noncompliance. 
 

  • LEARNING OBJECTIVES

 

  • After completing this course, you’ll be able to:
  • Articulate Packaging and Labeling’s role in product development
  • Ensure adherence to regulatory agency requirements
  • Anticipate potential obstacles in marketing, medical affairs, regulatory, legal or quality assurance

 

  • WHY SHOULD YOU ATTEND

Understanding the packaging and labeling process in the larger product development process will provide you an advantage in achieving success.

  • AREAS COVERED

 

  • After completing this course, you’ll be able to:
  • Articulate Packaging and Labeling’s role in product development
  • Ensure adherence to regulatory agency requirements
  • Anticipate potential obstacles in marketing, medical affairs, regulatory, legal or quality assurance

 

  • WHO WILL BENEFIT?

 

  • Operations Departments
  • Regulatory Affairs Departments
  • Labeling and Packaging Departments
  • Quality Assurance Departments
  • Production Control Departments
  • Packaging Technology Departments
  • Labeling Coordination Departments
  • Package Engineering Departments
  • Packaging Operations Departments
  • Project Management
  • Sales and Marketing Departments
     
  • SPEAKER

Michael Esposito has 30 years experience in the pharmaceutical industry and 13 years of 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.

Others Details

For more detail please click on this below link: http://bit.ly/33iaeB3 Email: [email protected] Tel: +1-(510)-868-1040

Registration Fees
Available
Registration Fees Details
Live session for 1 participant $199 Live + Recorded Session $269 Live + Transcript $249 Live + Training CD Free shipment within 72 hours from the date of webinar completion. $450 On Demand Options Transcript $179 Downloadable recorded session $239 Training CD Free shipment within 72 Hours, from the date of webinar completion $350 Group Session unlimited participants + Recorded $799
Registration Ways
Email
Phone
Website
Other
Address/Venue
  247compliance 2035 Sunset Lake, RoadSuite B-2, Newark, Delaware - 247compliance  Pin/Zip Code : 247compliance
Official Email ID
Contact

     +1-(510)-868-1040