|The registration for this conference has ended. You may still order CDs using the form below.||RegistrationCenter|
|Thursday, September 8, 2016|
|Add to Calendar|
|1:00 PM Eastern||12:00 PM Central|
|11:00 AM Mountain||10:00 AM Pacific|
Join Mark Vermette and Lyn Agostinelli of Halloran Consulting Group as they discuss the processes and procedures of document control from a quality systems perspective. Mark and Lyn will share their decades of experience in bringing solutions, including technology, to improve document control. They also bring a concrete perspective, based on real world insights, on what the FDA expects to see during an inspection of your facility.
This 1 hour webinar will cover:
Mark joined Halloran Consulting Group in 2015 with over 25 years of experience delivering technology, consulting services, and software in the life sciences industry. He has led system implementations for Clinical Trials Management Systems (CTMS), Electronic Data Capture systems (EDC), safety systems, data warehouses, content management systems, and analytics and reporting platforms.
Prior to joining Halloran, Mark was Vice President of Infosario Customer Engagement at Quintiles, Inc., where he founded and was responsible for the professional services organization leading technology integration and services delivery. He has held similar roles at CrossPhase Consulting, Galt Associates, and First Consulting Group. Mark also served as the product manager for CRIX International, a consortium of five pharmaceutical companies, the National Cancer Institute, and FDA with a mission to develop and service a shared platform for registration of physicians conducting clinical studies. Mark holds a Bachelor of Science from Davis and Elkins College in Elkins, West Virginia.
Lyn joined Halloran Consulting Group in 2010 bringing over 27 years of experience in the life science industry and clinical practice as a registered nurse. She has significant expertise managing clinical programs in pharmaceutical and device companies. Her proven clinical and project management skills give her the versatility that makes her equally comfortable with start-ups and established organizations.
Prior to joining Halloran, Lyn was a Site Manager at Boston Scientific where she developed and launched a remote monitoring group. In this capacity she implemented processes to govern the functions and managed the CRAs performing those activities. Prior to Boston Scientific, Lyn was a Clinical Affairs Manager at AAIPharma and oversaw the day-to-day activities of Research Associates and CRAs. At AAIPharma she also held interim project management roles ensuring projects were executed on time and within budget. Earlier in her career, she was a Project Director at the Asthma Research Center at Brigham and Women's Hospital. Lyn holds a Bachelor of Science in Nursing from the University of New Hampshire.
This is the third of 5 Compliance Thru Education webinars in the next 12 months.
TWO Special Offers!
Offer #1: Register for 3 webinars and get the 4th one at half price!
Offer #2: Register for 4 webinars this year and get the 5th one free!
Please use the following form to register for this webinar. You will receive an email confirmation shortly after you complete the registration.
If you are unable to register online or do not receive your confirmation email after registering (don't forget to check your Junk email folder), please contact our Registration Desk at 866-872-5840 (international callers please dial 617-502-2061). You can also contact us by email
COST: $239. AAHP members get a $90 discount with the promo code available from the AAHP.