Hello Everyone,

I wanted to give everyone the chance to join a free webinar packed with information about video marketing and how to make sales in this industry.

Time and Date: October 12, 2011 6:00 PM - 7:30 PM PDT

Hosted by Blake Goodwin. He is an entrepreneur and CEO of Video Optimize LLC specializing in Video Marketing for small businesses. He is giving away trade secrets and showing people how to start their very own marketing business. If you are interested in attending and want to sign up please go to http://www.blakegoodwin.com/join

There is a limited number of seats so please join early. If the webinar is full, I will post a message on the page linked above to let you know.

Note: This webinar starts at 6:00PM PST. This is not in the morning despite what it says in the title.

Who: Param Singh, vice president of clinical trial management solutions, BioPharm Systems

Adrian Hampshire, managing director, EMEA, BioPharm Systems

Paul Dobrowolskyj, senior consultant, Oracle Health Sciences

What: Webinar: "Business and Operational Risks in Clinical and Safety: Applying Appropriate Technology and Approaches to Mitigate Risk"

All business processes are subject to some level of risk. Key to the long term viability of any company is the critical need to identify the risks, quantify them, minimize them, and have a clear plan for dealing with any residual risks.

Organizations try to mitigate risks by implementing systems that support the company's business processes. Commercial software systems that are available from vendors such as Oracle include many capabilities which, if implemented properly, greatly reduce the risks in the business process.

The implementation of complex systems is, in itself, a risky process. Organizations like BioPharm Systems have been able to use their wide range of experience to develop pre-configured and pre-validated solutions that help reduce the risks during the implementation of a clinical trial management system (CTMS) and a safety system.

This one and a half-hour webinar will provide an overview of business risks related to clinical and safety systems and will illustrate how the risks inherent in implementing complex CTMS and safety systems can be significantly reduced.

When: Thursday, November 17, 2011 @:

7:00 a.m. US Pacific time
8:00 a.m. US Mountain time
9:00 a.m. US Central time
10:00 a.m. US Eastern time
15:00 UK time
16:00 Central European time

Webinar Information: To register for this complimentary webinar, go to: https://cc.readytalk.com/r/bf2hph6dutcu

Building an engaging cross-channel experience for your customers is more challenging than most organizations first think. Creating truly engaging customer interactions that capture interest and convert more business means addressing both outward facing customer experiences and the internal tools used in crafting the experiences.

Join us on Wednesday, November 9, 2011 at 11:00 am Eastern to learn more about:

• Customer engagement expectations

• Best practices for multi-channel experiences

• The engagement ecosystem? How does it all come together?

• Tools and technologies to help you capture and convert more business

• Tools and techniques for measuring success

Who is this session for?

This session is designed for medium to large organizations that are looking to create a new level of connection with their customers and manage cross-channel relationships. It is ideally suited for marketers, executives, and web managers.

Native Apps and HTML 5 web apps are two of the greatest technologies available now, for building solutions to reach and engage with Smartphone users.

Both technologies are providing some unique possibilities that can be leveraged for market research and consumer insights in the mobile world.

How do they compare in terms of taking advantage of Smartphone capabilities and user experience?

How easy or difficult are they from a solution development and maintenance standpoint?

What can the native apps do that web apps can’t and vice versa?

Which one should we choose for what purpose?

Is there a definite winner among these two?

Come; join us for these 45 minutes of hashing out the pros, cons and the overall approach that makes best sense.

The webinar is followed by a 15 minutes Q&A. So get ready not just to listen, but ask questions!

Who should attend?

* Consumer Insights and Market Research professionals
* Decision makers for Market Research / Survey platforms
* Decision makers for Mobile initiatives in consumer / market research field

Registration URL: https://www3.gotomeeting.com/register/176523182
Company URL: http://www.ipinionsurveys.com/

Why do we want to use Confirmed Opt-In?

Tune in to this webinar to find out exactly what Confirmed Opt-In is, what it does and why we want to use it in our email campaigns.

Get ready for an in-depth explanation about Confirmed Opt-In as well as hints and tips to ensure you get the highest amount of subscribers confirming to your list while at the same time making sure you don’t send any unsolicited email.

About the organization

Since 1998, Aweber has been a leader in the email marketing software field. Providing quality autoresponder services, newletter email marketing, email marketing analytics, html email templates & more, Aweber helps businesses stay in touch with the customers.

In this webinar we’ll review five key steps to get you on your way to getting a leg-up on your competition. If you’re looking to formulate a comprehensive competitive strategy or just to build competitive intelligence into your current marketing plan, this webinar will help you gain insight into how to use competitive intelligence tools to stay informed and adjust for shifts in your industry.

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.

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.

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.

Summary
This webinar will discuss current regulatory and quality requirements for reduced testing of components used in pharmaceuticals and medical devices. Reduced testing will be viewed from current industry practice, the regulations, and quality principles. The reduced testing lifecycle we studied and reviewed. This includes such topics as component specifications, material qualification, supplier auditing and qualification, collaborative laboratory testing, certificates of analysis, material validation sampling, analyzing testing, qualification, and disqualification. Examples of systems will be shown. This webinar will primarily use graphics, especially flowcharts, to demonstrate the principles and increase in understanding of the topics.

Details
Reduced testing test permits a medical product manufacturer to reduce testing of incoming components provided there are adequate controls on specification control, material qualification, supplier qualification & monitoring, material validation, and collaborative testing. Industry practice in the performance of reduced testing has resulted in new and modified expectations and requirements.

The benefits of systematic reduced testing program include increased compliance, smaller inventory cycles, less testing, less handling, and increased productivity and efficiency.

As industry has been looking to reduce costs, improve efficiency, the FDA has begun to more closely scrutinize the industry’s effort to make certain that the above mentioned controls are in place. In this effort the FDA is focusing on supplier control and sampling issues.
Why should you attend :

Reasons for attending this webinar include the following:
To understand the compliance and quality requirements for reducing incoming material testing on pharmaceutical and medical device components.
To gain knowledge applicable to the control and qualification of suppliers that will increase compliance and improve efficiency
To reduce costs and increase efficiency in the handling of incoming materials and components.

Areas Covered in the Session:

Advantages and disadvantages of reduced testing
Basic review of quality systems.
Brief review of regulatory requirements.
Differences between suppliers and contractors.
Interdepartmental roles in establishing and maintaining a reduced testing program.
A study of the reduced testing lifecycle in graphical format , including specification control, material qualification, researching and selecting suppliers, supplier auditing (including selection of audit team members) and qualification, corrective actions, handling certificates of analysis, maintaining supplier quality and control, supplier change control, and handling problems suppliers.
Logistics of implementing a reduced testing plan

Who will benefit:

Quality Control
Laboratory Manager
Warehousing Purchasing Managers
Procurement Managers
Laboratory Analyst
Cost Accounting

About the speaker:

Howard enjoys sharing his 30 years plus experience in starting up, developing, implementing, managing, and remediating pharmaceutical and medical device quality systems. One of his favorite areas is material and supplier control from which he receives great satisfaction in applying his knowledge for improvement.
He has a BS in Biology/Chemistry and Political Science as well as work toward an MBA. His ability to quickly learn the technology is demonstrated by his success in applying quality assurance principles to a wide range of pharmaceuticals and medical devices. He is a Certified Biomedical Auditor (CBA), Certified Quality Manager (CQM), and Quality Auditor (CQA). His technical education is further complemented by his Political Science degree helping him understand the regulatory process; his work toward an MBA provides business insight. He is a member of ASQ, PDA, AAMI, RAPS, and SQA.
He strongly believes that Quality is very influential in shaping successful operations. He knows how to use his leadership abilities to build organizational relationships that make systems operate effectively as well as to develop and empower people.