Live Webinar Proper Execution of Annual Product Reviews
01:00 PM EDT | 10:00 AM PDT | 12:00 PM CDT Duration 60 Minutes
Webinar Includes : All the training handouts , Certificate ,Q/A and 60 mins Live Webinar.
Join This course On March 01, 2017 at 01:00 PM EST at 01:00 PM EST | 12:00 PM CST | 10:00 AM PST
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.
Why Should You Attend?
This webinar will give a brief overview of the general procedure for the preparation and documentation of the Annual Product Quality Review and also focuses on the regulations and the regulatory requirements as per US and Europe. It will also 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.
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 Professionals
-- Quality Control Professtionals
-- regulatory affairs
-- supplier audit groups
Industries who can attend
This 60-minute online course is intended for professionals in the Medical Device, Biotechnology,Pharmaceutical Industry. Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel.