Clinical Data Systems,Webinar on Clinical Data Systems,Online Webinar on Clinical Data Systems,Clinical Data,FDA

Clinical Data Systems Regulated by FDA - online live webinar on January 2018 by Netzealous LLC DBA - Compliance4All

Webinar Information


Clinical Data Systems Regulated by FDA


Webinar Title
Clinical Data Systems Regulated by FDA
Event Type
Webinar
Webinar Date
12-01-2018
Last Date for Applying
11-01-2018
Location
Fremont, California, United States

Publish / Maintain / Marketing / Hosted By
Organization Name / Organize By
Netzealous LLC DBA - Compliance4All
Organizing/Related Departments
Trainings for all Industries
Organization Type
Organization/Company
Webinar Category
Both (Technical & Non Technical)
Webinar Level
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Accounting/Financial/Banking/Insurance

Manufacturing

Medical/Healthcare/Hospital

Location
Fremont, California, United States
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Overview:  
Companies engaged in the conduct of human clinical trials must adhere to specific government regulatory requirements.Certain documents, content and images related to a clinical trial must be stored and maintained, and depending on the regulatory jurisdiction.

Why should you Attend:
You should attend this webinar if you are responsible for establishing or maintaining a TMF, or providing quality assurance for data included in the file. This webinar will also benefit those involved in the conduct of clinical trials, audit and inspection of clinical trial study data and records, and submission of filings to regulatory agencies that involve clinical trial data. 

Areas Covered in the Session:

  • Learn what content is required for a TMF for a clinical tria
  • Learn about best practices and industry standards
  • Understand the importance of developing an effective Standard Operating Procedure

Who Will Benefit:

  • T Support Staff
  • QC/QA Managers and Analysts
  • Clinical Data Managers and Scientists
  • Compliance Managers and Auditors
  • Lab Managers and Analysts
  • Computer System Validation Specialists
  • GMP Training Specialists

Speaker Profile:
Carolyn (McKillop) Troiano has more than 35 years of experience in the tobacco, pharmaceutical, medical device and other FDA-regulated industries. She has worked directly, or on a consulting basis, for many of the larger pharmaceutical and tobacco companies in the US and Europe, developing and executing compliance strategies and programs.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

Others Details

For more details and updates please visit website.

Registration Fees
Available
Registration Fees Details
One Dial-in One Attendee Price: US$150.00
Registration Ways
Email
Phone
Website
Address/Venue
Online 
Official Email ID
support@compliance4All.com
Contact
Event Manager

Netzealous LLC DBA - Compliance4All 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA. Phone: +1-800-447-9407 Email: support@compliance4All.com

support@compliance4All.com

     18004479407
   Fax No: 302-288-6884
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