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Proper Management of Regulatory Inspections

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Website http://bit.ly/2ooxA31 | Edit Freely

Category Regulatory inspection, fda inspection readiness, Management of Regulatory Inspections, Quality Assurance, Regulatory agency inspections

Deadline: May 11, 2017 | Date: May 11, 2017

Venue/Country: New Hyde Park, U.S.A

Updated: 2017-04-20 17:47:27 (GMT+9)

Call For Papers - CFP

Overview:

The purpose of the Regulatory inspection is an activity that should demonstrate that your company is operating according to the proper CFR requirements and maintaining a state of compliance. The key to a successful audit is being able to communicate how your quality systems assure this state of control. Many times, the arrival of a Regulatory Investigator is a daunting experience for some. This webinar, you will learn how to properly alert key members that an investigator has arrived, the proper protocol for setting up the Inspection room and any associated “war” rooms that will support the inspection, and how to manage requests from the investigators in a timely and accurate manner. This preparation minimizes stress and disorder during the inspections.

Why Should You Attend:

To learn the how to set up support groups/rooms for the inspection.

Learn how to properly communicate with the inspector.

To be able to organize requests from the inspectors and process them in a timely and accurate manner.

Know what is expected of you and your company.

Learn what not to say or do during an inspection.

To learn how to use your internal Quality Assurance groups to help identify issues prior to an inspection.

Areas Covered in this Webinar:

Pre-planning and preparation activities

What to do when the investigator arrives

What documents to have ready and on hand

Assignments and responsibilities for the inspection

A review of Inspection Do's and Don'ts

The Opening and Close-out Sessions

Learning Objectives:

Upon completion of this session, attendees will learn the proper way to set up for a Regulatory Inspection, ensuring the inspection flows smoothly throughout the duration, and the proper way to speak to inspectors while they are performing the audit.

Who Will Benefit:

Site Quality Operations Managers

Quality Assurance personnel

Plant Managers and Supervisors

Manufacturing Superintendents and Managers

Individuals whose job knowledge and/or expertise may be called upon during an audit

Regulatory Affairs Managers

Speaker Profile:

Danielle DeLucy, MS, is an Independent Consultant to the Biologics and Pharmaceutical Industries.

Danielle DeLucy, 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:

http://bit.ly/2ooxA31

Email: referrals@complianceglobal.us

Toll Free: +1-844-746-4244

Tel: +1-516-900-5515

Fax: +1-516-900-5510


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.