Proper Execution of Annual Product Reviews

Posted By : User Ref No: WURUR47252 0
  • Image
  • TypeWebinar
  • Image
  • Location Newark, Delaware, United States
  • Price
  • Date 20-11-2019
Proper Execution of Annual Product Reviews, Newark, Delaware, United States
Webinar Title
Proper Execution of Annual Product Reviews
Event Type
Webinar
Webinar Date
20-11-2019
Last Date for Applying
20-11-2019
Location
Newark, Delaware, United States
Organize and Presented By
247compliance
Sponsored By
247compliance
Organizing/Related Departments
Medical Device
Organization Type
Event Organizing Company
WebinarCategory
Non Technical
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Medical/Healthcare/Hospital

Location
Newark, Delaware, United States
  • OVERVIEW

Annual Product Quality Review (APR) is an evaluation conducted annually to determine if there are any possible changes in the process or manufacturing of the pharmaceutical product or any change in the specifications of the product or any change in the manufacturing process. It is designed to minimize the product defects and also the risks associated with the manufacturing of the pharmaceutical product.

 

  • LEARNING OBJECTIVES
  • Discuss how to write APRs
  • Outline the requirements for APR reporting
  • Review what information to include in the reports
  • Discuss how well written APRs benefit your firm’s compliance

 

  • WHY SHOULD YOU ATTEND

This webinar will discuss the comparative evaluation about similarities and differences of requirements associated with the manufacturing of the drug product in different countries. It is also necessary to know that the regulatory requirements of different countries are different and hence this will further guarantee the quality of the pharmaceutical product.

 

  • AREAS COVERED

This webinar will review:

  • Annual Product Review definition
  • What needs to be included in the report
  • A model of an example Annual Product Review Report
  • Review of citations

 

  • WHO WILL BENEFIT?

Quality Assurance/Quality Control Directors, Managers, and Specialists 

Regulatory Affairs/Regulatory Compliance Directors, Managers, and Specialists 

Engineering/Development Directors, Managers, and Specialists

 

  • SPEAKER

Danielle DeLucy, MS, is owner of ASA Training and Consulting, LLC which provides Pharmaceutical and Biologics based companies with training and quality systems assistance in order to meet Regulatory compliance. Prior to this role, Danielle has been in the industry for 15 years serving in numerous Quality Management Roles, such as the Director of Product Quality, the oversight of Sterility Assurance practices and provided QA oversight of numerous filling and packaging operations. 

Others Details

For more detail please click on this below link: http://bit.ly/2Oh1hSG 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