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FDA Trends for CSV Compliance and Enforcement | Boston Seminar 2018

Start Date : July 25, 2018
End Date : July 26, 2018
Time : 9:00 am to6:00 pm

Phone : 800-447-9407
Email : globalcompliancepanel@gmail.com

Location :
Four Points by Sheraton Boston Logan Airport Revere, MA 407 Squire Rd, Revere, Massachusetts 02151, United States

Website

Description

Course "FDA Trends for Computer System Validation (CSV) Compliance and Enforcement" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.


Overview:


FDA requires that all computer systems used to produce, manage and report on "GxP" (GMP, GLC, GCP) related products be validated and maintained in accordance with specific rules. This seminar will help you understand the FDA's current thinking on computer systems that are validated and subject to inspection and audit.


As a "GxP" system following Good Manufacturing, Laboratory and Clinical Practices; the computer system must be validated in accordance with FDA requirements. If electronic records and/or electronic signatures (ER/ES) are incorporated into the system, FDA's CFR Part 11 guidance on ER/ES must be followed.


This seminar will focus on the key areas that are most important, including security and data integrity. Implementing and following the System Development Life Cycle (SDLC) methodology is the best approach for Computer System Validation and maintaining data integrity. The life cycle approach takes all aspects of validation into account throughout the life of the system and the data that it houses. The data is a key asset for any FDA-regulated company and must be protected through its entire retention period.


Why you should attend:


FDA requires all computer systems that handle data regulated by the Agency to be validated in accordance with their guidance on computerized systems. This guidance was first issued in 1983, and the main points of focus remain consistent today, despite the number of years that have passed and the technology changes that have taken place.


The guidance was revisited for its application to the medical device industry, as the first issuance addressed pharmaceuticals. In 1997, 21 CFR Part 11 was issued to address electronic records and signatures, as many laboratories and other FDA-regulated organizations began seeking ways to move into a paperless environment. This guidance has been modified over the years to make it more palatable to industry, and this includes discretionary enforcement measures. The intent was to avoid creating a huge regulatory compliance cost to industry that was initially preventing companies from embracing the technology.


This session will provide some insight into current trends in compliance and enforcement. Some are based on technology changes, and these will continue to have an impact as new innovations come into use in the industry.


Areas Covered in the Session:





Who Will Benefit:


Personnel in the following roles will benefit:



Agenda:


Day 1 Schedule




Lecture 1 (90 Mins):





Lecture 2 (90 Mins):





Lecture 3 (90 Mins):





Lecture 4 (90 Mins):



Day 2 Schedule




Lecture 1 (90 Mins):





Lecture 2 (90 Mins):





Lecture 3 (90 Mins):





Lecture 4 (90 Mins):



 


Speaker


Carolyn Troiano





Carolyn Troiano has more than 35 years of experience in Computer System Validation in the pharmaceutical, medical device, tobacco and other FDA-regulated industries. She is currently an independent consultant, advising companies on FDA compliance, Computer System Validation and large-scale IT system implementation projects. Carolyn participated in the Industry/FDA partnership that developed 21 CFR Part 11, the FDA's guidance on electronic records and electronic signatures (ER/ES).


 


Location:  Boston, MA Date: June 25th & 26th, 2018 and Time: 9:00 AM to 6:00 PM


Venue:  WILL BE ANNOUNCED SOON


 


Price:


Price: $1,295.00 (Seminar Fee for One Delegate)


Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*


Register for 10 attendees Price: $7,122.00 $12,950.00 You Save: $5,828.00 (45%)*


Register now and save $200. (Early Bird)


Until May 10, Early Bird Price: $1,295.00 From May 11 to June 19, Regular Price: $1,495.00


Sponsorship Program benefits for “FDA Trends for CSV Compliance and Enforcement” seminar


For More Information- https://www.globalcompliancepanel.com/control/sponsorship 


Contact us today!


NetZealous LLC DBA GlobalCompliancePanel


john.robinson@globalcompliancepanel.com  


Toll free: +1-800-447-9407


Phone: +1-510-584-9661


 Website: http://www.globalcompliancepanel.com


 


Registration Link - https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901786SEMINAR?SEO


 


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Registration Info

https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901786SEMINAR?meetings4docs_june_2018_seo

Contact the Organizer

Organized by

Organized by globalcompliancepanel

NetZealous LLC DBA GlobalCompliancePanel ,
161 Mission Falls Lane,suite 216

FDA requires that all computer systems used to produce, manage and report on "GxP" (GMP, GLC, GCP) related products be validated and maintained in accordance with specific rules

Tel: 8004479407
Mobile: 8004479407
Email: globalcompliancepanel@gmail.com
Website: https://www.globalcompliancepanel.com


Event Categories: Health & Nutrition and Physical Medicine.




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