How to Select and Manage Vendors in a Regulated Environment (incl. ICH E6)

Instructor: Angela Bazigos
Product ID: 705488
  • 11
  • December 2017
  • 10:00 AM PST | 01:00 PM EST
    Duration: 90 Min

Live Online Training
December 11, Monday 10:00 AM PST | 01:00 PM EST | Duration: 90 Min

One Dial-in One Attendee
Group-Max. 10 Attendees/Location
(For Multiple Locations Contact Customer Care)
Super Deal - Get CD free!

recorded version

1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section 48 hrs after completion of Live training

Training CD / USB Drive

One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days after completion of Live training

Combo Offers

Live + Recorded Version


Live + Training CD/USB


Customer Care

Fax: +1-650-565-8542


Read Frequently Asked Questions

Buying software is a fact of life for most companies. There is fierce competition in the market, with multiple software vendors trying to convince to buy their product. How do you determine whether to buy the software or having it built in house? Or which vendor to choose? And if you buy something, how do you determine whether to have it hosted? And are there any regulations that apply to this software? And if so, what are they?

Why Should You Attend:

This presentation will give the answers to these questions; plus show you ‘hidden’ issues that will save you from:

  1. Selecting and implementing the wrong system that ends up costing more in trying to get a ‘square peg to fit in a round hole’ efforts, often resulting in cost and time overruns and finally ending up not being used by the user community.
  2. Duplicating data in systems with overlapping functionality resulting in both duplication of effort and higher incidence of errors
  3. Inadvertently acting as the vendor’s beta site
  4. Putting unnecessary work into meeting regulations

Even though this presentation focuses primarily on software, the hardware required will also be addressed.

Areas Covered in the Webinar:

  • To buy or to build?
  • Why not stay with the existing solution?
  • Who should be part of the evaluation and decision team?
  • What is involved in the assembly of selection requirements?
  • What is the vendor evaluation process?
  • How does the new software fit into your current environment without causing errors and duplication?
  • What are the regulatory requirements for:
    • An In-House Build Solution?
    • A Commercial Off The Shelf Solution?
    • A Hosted Solution
    • Hardware environment
    • Implementation Consultants?
    • How do you use Risk Assessment?
  • How do you manage consultants and vendors?
  • How do you leverage the vendors’ methodology?
  • How long does it take and what will it cost?

Who Will Benefit:

  • CEO
  • Regulatory VP
  • Quality VPs
  • IT VPs
  • Database Administrators
  • System Administrators
  • Validation Specialists
  • Security Specialists
  • Regulatory Affairs professionals
  • Quality Managers
  • Quality Engineers
  • Small business owners
  • GxP
  • Consultants
Instructor Profile:
Angela Bazigos

Angela Bazigos
CEO, Touchstone Technologies Silicon Valley Inc

Angela Bazigos, is the CEO of Touchstone Technologies Silicon Valley, Inc. "Knowledge is Power". She has 35 years of experience in the Lifesciences industry spanning GLP, GCP, GMP, Medical Devices & 21 CFR 11 and has a patent aimed at speeding up Software Compliance.

Ms. Bazigos is a Past President of PRCSQA, a member of the SQA CVIC, ASQ, DIA and RAPS. She works closely with the FDA on behalf of her clients. She consults to LifeScience Investment Groups as well as to Pharma / Biotech / Medical Device companies on compliance matters, including strategy, submissions, quality assurance and remediations following action by the FDA.

More recently, Ms. Bazigos co-authored Computerized Systems in Clinical Research / Current Data Quality and Data Integrity Concepts with FDA, DIA and Academia. She was on the board for UC Berkeley’s Business School for Executive Education in Life Sciences and is now on the Stanford Who’s Who Registry for contributions to the Lifesciences industry.

Topic Background:

Software is widely used in our industry and selection of new software or upgrade of existing software is one of the activities that crop up every year in an IT department’s task list. Our industry, has the added challenge of being subject to both regulations that add another degree of complexity to this already complex task.

Follow us :
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices
Seminars by Ex-FDA Officials

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email call +1-888-717-2436 (Toll Free).

Product Reviews

This product hasn't received any reviews yet. Be the first to review this product! Write review

Best Sellers
You Recently Viewed