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« Wednesday October 27, 2010 »
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Monitoring Impurities in Pharmaceutical Products to meet ICH Q3 A/B Requirements - Webinar By ComplianceOnline
Start: 10/27/2010 10:00 am
End: 10/27/2010 11:00 am

 This pharma training will discuss how to monitor impurities in pharmaceutical products as per ICH Q3 A/B requirements and learn how to measure the thresholds to report for regulatory submission.
 
Learning Objectives:
Upon completion of this session, attendees will understand regulatory requirements in the monitoring of pharmaceutical impurities. Participants will gain practical knowledge about key considerations when reporting impurities for regulatory submission. This session will also discuss observations and infractions that were obtained due to recoding impurities in pharmaceutical labs.
Areas Covered in the Seminar:

  • Understand regulatory expectations.
  • Discuss warning letters and citations.
  • Understand regulatory requirement guidelines surrounding impurities in API and Drug Products.
  • Review ICH Q3A for controlling impurities in API and Q3B for impurities in Drug Products.
  • Understand different thresholds to report for regulatory submission.

Who Will Benefit:
To get the most out of the course, we highly recommended that you have at least two years of pharmaceutical analysis or drug development experience.

  • R&D analysts
  • QA and QC Managers
  • Regulatory scientists
  • Directors

 

The Case for Social Media Management and Archiving
Start: 10/27/2010 10:00 am
End: 10/27/2010 11:00 am

A live Webinar sponsored by FaceTime, Smarsh and Messaging News

Date & Time:

Wednesday, October 27, 2010
1:00pm EDT / 10:00am PDT / 18:00pm BST / 19:00 CET

Speakers:

  • Michael Osterman, Principal, Osterman Research, Inc.
  • Norv Leong, Product Marketing Manager, FaceTime
  • Sam Kolbert-Hyle, VP/Business Development & Strategic Initiatives, Smarsh

We will randomly select one registrant for this Webinar to receive an Apple iPad. The winner will be announced during the live event.

Register now for “The Case for Social Media Management and Archiving”

The use of social media in companies has literally exploded over the past few years in virtually every organization. Yet relatively few organizations understand how it is being used, many are taking on needless legal, compliance, and reputational risks, and most IT professionals have not made the return-on-investment case internally for social media management and archiving solutions.

Join us for a special Osterman Research and Messaging News panel Webinar focused on why organizations should monitor and archive social media content and how you can justify implementing a solution in your organization.

Attendees will be able to articulate the ROI case internally for archiving and risk mitigation arguments that should be used to help quickly gain control of social media content while still experiencing its benefits. Discover:

  • What are the risks associated with doing nothing to manage the use of these tools in a corporate environment?
  • What are the best practices around social media policies and options to consider for your organization?
  • What are some of the leading solutions available to help you manage and archive social media content, and to ensure that social media is not used in violation of corporate policies?
  • What are some of the key regulations which govern social media and its archiving?
  • What are the latest trends in social media and management and archiving of this content?

In short, understand why you need to archive and manage social media, how to make the ROI case for it internally, and have the opportunity to ask your top social media management questions of our experts.

Register now for “The Case for Social Media Management and Archiving”

QSR Device Inspections – Transition from “Barely Surviving” to “Gaining Control” - Webinar By ComplianceOnline
Start: 10/27/2010 10:00 am
End: 10/27/2010 12:00 pm

 This Medical Device Quality System training will discuss how to Create an adequate quality system that meets FDA’s requirements and Effectively prepare for upcoming Quality System Regulation (QSR) inspections.
 
Areas Covered in the Seminar:

  • Definition of Quality System Regulations (QSR).
  • Who must comply fully vs who is allowed to partially comply to QSR.
  • Definition of QSR’s four main subsystems:
    • Management Control
    • Corrective and Preventive Action (CAPA)
    • Design Controls
    • Production and Process Controls (P&PC)
  • Definition of Satellite subsystems.
    • Medical Device Reporting
    • Corrections and Removals
    • Medical Device Tracking
    • Sterilization Process Controls
  • Tips on establishing an effective quality system for the design, production and distribution of your device.
  • Overview of Quality System Inspection Technique.
  • Typical Quality System deficiencies noted in Warning letters.
  • Techniques used in inspection planning.
  • Factors involved in selection process.
  • Overview of FDA regulations and guidelines used for inspections.
  • Inspection documentation and proper follow-up procedures.
  • Tips for Preparing for Quality System Inspection/

 

FREE Webinar: Generate Quality Sales Leads Using Webinars
Start: 10/27/2010 11:00 am

Generate Quality Sales Leads
~Using Webinars

Webinars are a low cost way to generate qualified sales leads. Delivered as educational marketing, they also position you as an authority in your field, creating respect and instilling trust in your audience. Bottom line, it gives your sales efforts a running start.

What You Will Learn:
• The benefits of educational marketing
• The rules of lead generation webinar engagement
• The steps to create a well organized follow-up process
• The best methods to cost-effectively attract webinar registrants

Who Should Attend:
• Sales and Marketing professionals who know the value of their customer
• Management who wants their sales staff closing, not cold calling
• Executives who understand long-term leadsource ROI

All Attendees will receive: a copy of “40 FAQs About Lead Generation Webinars"

About the Presenter:
Don Cameron, Marketing Strategist and founder of Interactive Telesis and ConferTel, has helped hundreds of organizations generate non-dues revenue by delivering educational webinars to their members in addition to helping businesses use an educational marketing approach to cost-effectively generate qualified sales leads.

Webinar on Business Continuity with Virtualization on Oct 27, 2010
Start: 10/27/2010 11:12 pm

Register for the webinar on Business Continuity with Virtualization and how to maximize performance while Minimizing TCO on Oct 27th 2010. Once registered you will receive an email confirming your registration with information you need to join the Webinar.

Most IT managers are continuing to look for ways to save money in the IT enterprise. One of the chief concerns for IT professionals is implementing a Business Continuity/Disaster Recovery solution. This webinar is designed to show you how to manage Business Continuity with Virtualization.

Raj Kosuri, CTO and Terell Jones Director of Infrastructure for Ecomnets, the industry's leading authorities on Green IT infrastructure design and management will discuss:
• Why use virtualization as a business continuity strategy?
• How does it maximize performance?
• How does it minimize TCO?

Who Should Attend: Professionals new to virtualization including: CEO, CIO, CTO, CFO, CSO, COO, IT Managers, Data Center Managers, Facilities Managers, Business Managers

About EcomNets:

EcomNets Green IT Solutions can help you save energy costs, save cooling costs, and reduce your carbon footprint. EcomNets are experts in PC Power Management, Virtualization, Cloud Computing, Data Center Best Practices, and Electronic Waste Management. EcomNets can help you easily develop a Green IT strategy compatible with your business processes. EcomNets Green IT Solutions delivers fast, flexible, and affordable solutions, helping you drive consistent and measurable improvements in your Green IT Initiatives.

www.EcomNets.com

Register for a session now by checking a date below:

Wed, Oct 27, 2010 11:00 AM - 12:00 PM EDT
https://www1.gotomeeting.com/register/238994081

Wed, Dec 1, 2010 11:00 AM - 12:00 PM EST
https://www1.gotomeeting.com/register/869060065

Wed, Jan 12, 2011 11:00 AM - 12:00 PM EST
https://www1.gotomeeting.com/register/210026305

Once registered you will receive an email confirming your registration with information you need to join the Webinar.

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