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Proper Execution of Annual Product Reviews
Presented By 247compliance
Wednesday, November 20th at 1:00pm EST
Online sale ends: 11/20/19 at 12:00pm EST
247compliance.com
247compliance 2035 Sunset Lake, RoadSuite B-2, Newark, Delaware - 247compliance
newark, DE 19702
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Talent

Danielle DeLucy

Description
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. 


For more detail please click on this below link:
Email: support@247compliance.com
Tel: +1-(510)-868-1040


Presented By

1:00pm to 2:00pm
Doors open at 1:00pm

General Admission: $199.00

Age
All Ages

247compliance.com<br> 247compliance 2035 Sunset Lake, RoadSuite B-2, Newark, Delaware - 247compliance<br> newark, 19702

+1-(510)-868-1040

Medical Devices

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UPCOMING EVENTS
Friday, November 15th

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Friday, November 15th

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PAST EVENTS
Wednesday, November 13th

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Wednesday, November 13th

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Wednesday, November 13th

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