- Time:
- 12:30am-2:00am
- Description:
- Globalskywatch.com is a website documenting news and information about stratospheric geoengineering. there is a guest speaker and then open mike to discuss problems and concerns about the climate mitigation program.
- Time:
- 2:00pm-3:15pm
- Description:
- This training will teach you how to prepare for a medical staff professional review adverse action hearing, including what steps are necessary to afford the respondent practitioner due process.
Why Should You Attend:
It sometimes becomes necessary for the medical staff to recommend to the governing board that the medical privileges of a practitioner either be removed or denied. Before such an adverse action is taken, it is very important that the practitioner is afforded due process. That requires planning.. It is extremely important to have set the stage properly.
This session will provide the perspective of a hearing officer as to what steps should and must be taken before a corrective action is taken and how to prepare for the hearing. Specifically, actions that should be taken and should not be taken will be discussed.
You will learn how to prepare for a medical staff professional review adverse action hearing, including what steps are necessary to afford the respondent practitioner due process. You will learn what is required to conduct an adequate investigation, what type of notice to the affected practitioner should be given, how to develop clear and concise bylaws, fair hearing policies and other directives, and the type of documentation that is necessary to support the adverse action taken or to be taken.
Areas Covered in this Seminar:
- Clear and concise bylaws, policies and other directives
- The investigative process
- Criteria for admission to the staff
- Information required to support the application
- Membership on other staff
- References
- Following the fair hearing plan
- Notice
- Hearing
- Reasons for the adverse action
- Documentation required to support an adverse action
- Time:
- 2:00pm-3:00pm
- Description:
- A book is the best marketing investment you can make. It gives you a platform to grow your business. Everyone who reads your book is a potential customer and there is nothing more effective as a marketing giveaway than a book.
Many people dream of writing a book but most people never put pen to paper. Discover the the depth of value a book (or series of books) can create for your business.
Attendees will learn how a book:
*Can make you an instant expert.
*Can help you build a brand.
*Can drive lead generation.
*Can increase revenue with both new and old clients.
*Can help you get speaking engagements.
*Can be repurposed into many different types of content.
Whether you write the book yourself, have your clients or partners provide content, or have it ghostwritten, you will be informed and inspired by the stories and lessons of others who have had success with books.
About Your Presenter:
Mitchell Levy, CEO, Thought Leader Creator, and Publisher at THiNKaha®, has started and run fifteen firms and partnerships since 1997. He and his teams focus is to help turn corporate experts into thought leaders. He is a physical and eBook publisher (225+ titles) and an Amazon best-selling author with eighteen business books including “42 Rules for Driving Success with Books (2nd Edition)”. Mr. Levy is a frequent media guest and a popular speaker. In addition to the companies/joint ventures he's started, Mr. Levy has provided strategic consulting to over 100 companies, has advised over 500 CEOs on critical business issues through the CEO networking groups he's run, and has been Chairman of the Board of a NASDAQ listed company.
- Time:
- 2:00pm-3:00pm
- Description:
- This pharmaceutical water systems webinar training will discuss what you should do when your monitoring data tells you that you may have a significant biofilm problem. It covers how to verify that the data and your interpretation of the data are correct, as well as the location of the problem which gives you clues as to what caused the problem and its impact on manufacturing and product.
Why Should You Attend:
Unfortunately, the point when some personnel begin to think about the possibility of having biofilm is after it may have already gotten out of control. Any Gram negative microbial counts at all means you already have biofilm, but when counts approach your process control levels, it usually means that biofilm is rampant, thick and out of control. If it is not brought back under control quickly, it will get much worst.
This webinar will not only allow you to recognize when biofilm has gotten out of control, but also, very importantly, how to bring it back under control and assuring it has been effective. But these measures are generally very extreme and not something you would want to routinely execute. So finding and attacking the source of the problem will allow you to understand how to prevent it from recurring and having to go through these extreme mitigation efforts yet again.
This webinar also covers the extraordinary sanitization strategies you can use to kill and remove the biofilm, and importantly, verifying the success of your efforts. These efforts are far more involved than routine microbial controls, so effective prevention is far better and cheaper than mitigating it after it has gotten out of control.
Areas Covered in this Webinar:
- Are you sure there is a problem?
- What is the scope of the problem?
- What caused the problem?
- What can remediate the problem?
- What can prevent its recurrence?
- Are you sure it worked?
- Prevention is far easier than remediation!
- Time:
- 5:00am-5:30am
- Description:
- Monthly webinars for entrepreneurs.
30 minutes of helpful + uncomplicated
business advice each month.
For free.
I know you’re busy.
And I know you don’t have time for sales pitches disguised as information.
The Training Circle is a monthly call for entrepreneurs + small businesses.
No sales pitches, no padding.
Just quick, instantly-implementable ideas for your business.
- Time:
- 1:00pm-2:00pm
- Description:
- In a live webinar, Chris Ling, Financial Controller at British Gas, will explain how the company has re-examined its finance processes, and simplified these to improve performance for the business and its stakeholder groups.
Chris will share his tips on:
• how Finance can take on the business partnering role;
• how to maximize efficiencies through an enterprise-wide (end-to-end) view on processes;
• how to drive integrated process improvements on-site and offshore;
• how to drive a culture of continuous improvement through Finance transformation.
- Time:
- 2:00pm-3:30pm
- Description:
- This training on fraud awareness program will discuss recent history and profile of fraud cases and will help attendees understand specific processes and techniques needed to be effective when providing assistance on fraud issues.
Why Should You Attend:
Many organizations don’t think about the fraud issue until something has occurred or been identified and they need someone to perform an investigation. Inherently, organizations strive to ensure the individuals they hire are honest and ethical. In the same vein, executives often find themselves avoiding the open topic of fraud awareness because of the concern that “fraud awareness may lead to people committing fraud”. However, this very fact can itself contribute to an atmosphere that allows inappropriate behavior to happen. Depending upon the fraud perpetrated, the professional who takes on the investigative and examination role may vary. However, all compliance and risk professionals can perform a vital role in their organizations’ anti-fraud program.
Most organizations would agree that pro-active identification of risks is more beneficial than reactive mitigation. Similarly, pro-active process for training and educating the employee population about fraud can serve a much greater benefit than simply reacting to identified instances.
This webinar will discuss recent history and profile of fraud cases and how the fraud triangle can be utilized in awareness and mitigation techniques. It will also discuss fraud concerns for 2013 and the key concepts of fraud awareness. It will make attendees familiar with the root causes of fraud and compliance and risk professionals’ role in communicating and training on fraud awareness.
Areas Covered in the Webinar:
This session will cover the following learning objectives:
- Recent history and profile of fraud cases
- How the fraud triangle can be utilized in awareness and mitigation techniques.
- Understanding and identifying those process most susceptible to fraudulent activity.
- Fraud red flags and process awareness.
- Fraud concerns for 2013 and key concepts for fraud awareness
- Understanding the fraudsters profile and the root causes of fraud
- The compliance and risk professionals role in communicating and training on fraud awareness
- Time:
- 3:00pm-4:30pm
- Description:
- Starts Tuesday, April 2, 2013, weekly
12 weeks, 11am-1230pm EDT, on your Desktop
Conducted by Steve Bender
Discounts available for groups
Free registration or cash back available for referrals
Graduation certificates available
To watch free orientation video: http://www.qualityconn.com/Webinar-Free-CSTE-Intro-Dec-5-2012.htm
The CSTE Common Body of Knowledge (CBOK) skill categories have been selected to address the challenges faced by today’s software testers. The Web-based CSTE Exam Study Course is a live, facilitated discussion and presentation of the ten CBOK skill categories. The course reinforces current knowledge, re-introduces concepts that may not be used everyday, explains the rationale for use, and highlights both multiple choice and essay type sample examination questions and responses.
- Time:
- 5:00pm-5:30pm
- Description:
- Join us for a 20 minute webinar as we focus on the issues a "seat of the pants" estimating practice has and how cost estimating software such as Costimator can help overcome these problems.
- Time:
- 7:00pm-8:00pm
- Description:
- You are invited to LeadMaster's webinar that takes place every Tuesday at 11:00am PST/2:00pm EST
LeadMaster is an affordable web-based Lead Management System which enables companies to close the loop between marketing and sales.
See an overview of LeadMaster's capabilities
This webinar will demonstrate how to:
- Navigate the LeadMaster system
- Use LeadMaster based on role, i.e. Sales Manager, Marketing Manager, Sales Rep
- Assign and distribute leads
- Create and send e-mail marketing and lead nurturing
- Manage opportunities and quotes
- Build workflow automation
Register for the next webinar at this link http://www.leadmaster.com/LeadMaster-Library/Tues-Webinar/webinar.html
- Time:
- 8:00pm-8:40pm
- Description:
- Steps Your Business Can Take to Mitigate the Risks and Ensure a Smooth Transition to The Cloud
This webinar is for executives who are serious about cloud computing, but are unsure of how to securely and efficiently make the transition.
We've done the reseach for you.
When researching cloud options, it's important to understand the risks, bottlenecks, and productivity traps of moving to a cloud computing provider.
During this webinar, you'll learn:
1.The Signs It’s Time To Migrate To The Cloud
2.Steps To Managing Cloud Expectations
3.How to Identify & Mitigate the Cloud Risks
4.How to Ensure a Smooth Transition To The Cloud
(If you're a cloud computing beginner, you may want to start with our 'Cloud Computing 101' webinar)
- Time:
- 10:00pm-11:00pm
- Description:
- This webinar series is for anyone, young or old, who is interested in learning how to create economical and professional podcasts for distribution through hosted podcasts sites as well as iTunes.
Learning how to do podcasts could be the first step
for you to transform your life!
"4 Step By Step Webinars to Podcast Your Way to Riches"
May 28, 2013
June 4, 2013
June 12, 2013
June 18, 2013
At 6:00 pm PST
Reserve your spot at
- Time:
- 1:00am-4:00am
- Description:
- Shalonda 'Treasure' Williams is honored to invite you to the Motivation For Today Empowerment Call. Every Wednesday night at 9 p.m. EST, you will join Coach Treasure, as she is affectionately called, as she equips, inspires, motivates, encourages and even challenges you to live out your best life yet! The life where you know just who you are and what you have to offer! Each week there will be a different topic fir to empower You to T.A.P. into your true worth... Spirit! Soul! & Body! Join us on facebook for a daily dose of motivation and for call updates!
- Time:
- 2:00pm-3:30pm
- Description:
- This training on data security will provide the tools to design and implement effective IT control structures and audit programs to help comply with the current data privacy and confidentiality regulations.
Why Should You Attend:
With the growth of social media networking and use of computer systems in storing confidential data, non-compliance with privacy laws in various countries has led to record penalties. Management and auditors of organizations using cloud computing or other technologies to store confidential data/personal information of individuals have an obligation in terms of legislation to ensure the confidentiality as long as the data remains within their sphere of responsibility. Failure to do so can have major implications in terms of both reputational risk and even long-term survival of an organization. Internal audits play a vital role in ensuring corporate compliance and ongoing effectiveness of appropriate control structures.
This training will explain the methods to comply with current data privacy regulations. It will help the attendees in understanding and implementing an effective control structure and internal audit program within the organization. It will also discuss the auditor’s role in evaluating privacy control structures and the use of continuous monitoring in order to comply with privacy legislation.
Areas Covered in the Webinar:
This webinar will discuss the following topics:
- Current privacy legislation.
- Designing an effective control structure.
- The effect on risk of developments within information technology.
- The auditor's role in evaluating privacy control structures.
- Implementing an effective audit program.
- The use of continuous monitoring.
- Time:
- 2:00pm-3:30pm
- Description:
- This training on FDA cGMPs for Dietary Supplements and Nutraceuticals will discuss current FDA regulations, GMP requirements and techniques to be compliant using easier, shorter and convenient strategies. Case studies of FDA audit experiences will be presented for easy understanding.
Why Should You Attend:
In the last 4 years the number of FDA warning letters to manufactures of dietary supplement manufacturers have seen a significant increase. FDA now requires manufacturers of dietary supplements to follow GMP requirements closer to those for drugs than those for foods. These requirements include stricter documentation, standardized processes, use of trained personnel, adequately designed facilities, quality testing, packaging and shipping, and audit trails of processes. These requirements have created lots of anxiety in an industry filled with small businesses with few products, and international companies marketing in the US.
If you are a manufacturer, importer, supplier, stocker, marketer, shipper, or user of dietary supplements, this training is for you. The webinar will describe the US GMP requirements and discuss techniques to be compliant using easier, shorter and convenient strategies. The presenter will discuss ways to demonstrate compliance to the current regulations and regulatory trends for the near future. Common findings and possible solutions will be discussed. Case studies will be presented for audit experiences in many countries including US, China, Israel, Taiwan, and India.
Areas Covered in the Seminar:
- Key manufacturing issues related to dietary supplements and nutraceuticals.
- Raw material sourcing, validation, accountability, and documentation techniques.
- Facility design and planning issues.
- SOP and training requirements.
- How do these changes impact products currently in the market.
- Techniques to ensure compliance at international manufacturing sites.
Learning Objectives:
Learn how to be compliant with current GMP requirements in the US for dietary supplements in less than an hour to increase credibility of existing products and make it easier to launch more products in the US market in the near future.
- Time:
- 8:00am-9:00am
- Description:
- Are you ready to grow your business yet in order to do this you need more income?
Do you want more clients - knowing you can serve them, but the thought of having to sell your services in order to get them makes you just cringe?
Do you break out in the cold sweats whenever you get ready for a conversation with a potential client?
Or worse yet...
Do you avoid having sales conversations altogether, if you can?
If so, then guess what? You've got a case of the Divinely Broke™ Sales Dilemma. (Didn't know there was a name for it, didja?)
But here’s the good news: you can overcome it!
I’ll be sharing how on a complimentary, dare I say yummy training call on Tuesday, June 18th at 4:00 pm Eastern.
http://divinelyintuitivebusiness.com/sacred-sexy-sales-preview-call
If you’re ready to unlock the secrets to having fabulously fun sales conversations, then get signed up and my Divine team will get you the call-in details right away.
- Time:
- 2:00pm-3:00pm
- Description:
- This webinar will provide perspective on how cosmetic companies should label their products for the US market, and what needs to be considered in order to substantiate the advertising claims being made for such products.
Why Should You Attend:
The cosmetic product industry is growing rapidly in the United States with an increasing population of consumers taking an active role in maintaining and improving their physical appearance. The expansion of product offerings in this category has been met by an increase in monitoring and enforcement by the FDA and FTC, especially as ingredient technologies and formulations deliver therapeutic benefits. It is therefore important for cosmetic companies to ensure their product labels and accompanying claims are fully compliant with applicable statutes and regulations.
This session is designed for cosmetic companies, and is focused on helping those companies develop product labels and advertising claims that comply with applicable statutory and regulatory requirements. The webinar will also provide a perspective on how regulatory compliance can be built into company programs to support the development and launch of cosmetics in the US.
- Time:
- 2:00pm-3:00pm
- Description:
- This HR compliance training will clearly explain how you can adapt compliant HR best practices in setting up a virtual workplace plan. It will discuss the key elements, dos and don’ts of effective HR program implementation in a virtual workplace environment.
Why Should You Attend:
Technology at lightning speed continues to reduce the global gap and virtual workplaces are everywhere as an expectation and is even used in some companies as a way to reduce overhead costs. Some employees have never known any kind of workplace but a virtual one. Working virtually has overnight become so mainstream that in some respects you're almost considered "old school" if your business doesn't at least allow it for some jobs.
But as more and more employees flood into a hodgepodge of largely individually negotiated work "agreements", the problems can begin. It seemed easy - employees could just work in a different place, but actually it turned out to be a different way of working. So as they say - fail to plan, then plan to fail.
This HR compliance webinar will discuss in detail the compliance hotspots and considerations of different HR laws implementation in a virtual environment. From job identification issues, existing policy revisions, clarifying performance expectations, having to plan communications, and different methods of employee selection, it will cover all important matters that need careful consideration and planning in a virtual workforce.
It will help attendees to identify how to foster teamwork between people who never traditionally meet or even seen each other.
Areas Covered in the Seminar:
- They Did WHAT? Compliance hot spots and considerations; exempt/non-exempt timekeeping, FMLA, safety, data security and more.
- Not all high performance translates to a virtual workplace - identifying virtual high performers, both new hires and within existing employees.
- Out of sight doesn't have to equal out of mind. Managing performance from afar through objectives and expectations.
- Reorganizing current virtual arrangements and setting up processes for new ones. Tips for transitioning workforces.
- When "working in your pajamas" doesn't. Pitfalls of virtual workplaces.
- Making time to communicate. Dos and Don'ts for a virtual manager.
- How to foster teamwork between people who never traditionally met or even seen each other.
- How to move people back to a traditional workplace or move them on.
- Time:
- 11:00pm-11:20pm
- Description:
- How to Generate Thousands of Potential Leads on Twitter
In this short, but effective 17 minute FREE webinar you will leave knowing how to:
- Identify laser focused leads
- 3 easy ways to increase your visibility on Twitter
- Avoid the #1 mistake small businesses make on Twitter
This webinar is perfect for entrepreneurs and small business owners who have been frustrated with their results or lack of results on Twitter. Limited places available, reserve your spot by registering TODAY.
When: Thursday, June 6th, 1:00 EST, 7:00pm CET
- Time:
- 8:00am-9:00am
- Description:
- Are you ready to grow your business yet in order to do this you need more income?
Do you want more clients - knowing you can serve them, but the thought of having to sell your services in order to get them makes you just cringe?
Do you break out in the cold sweats whenever you get ready for a conversation with a potential client?
Or worse yet...
Do you avoid having sales conversations altogether, if you can?
If so, then guess what? You've got a case of the Divinely Broke™ Sales Dilemma. (Didn't know there was a name for it, didja?)
But here’s the good news: you can overcome it!
I’ll be sharing how on a complimentary, dare I say yummy training call on Tuesday, June 18th at 4:00 pm Eastern.
http://divinelyintuitivebusiness.com/sacred-sexy-sales-preview-call
If you’re ready to unlock the secrets to having fabulously fun sales conversations, then get signed up and my Divine team will get you the call-in details right away.
- Time:
- 2:00pm-3:00pm
- Description:
- This webinar on clinical study design will explore the differences among superiority, Non-inferiority (NI), and equivalence trials, including development of the precise research questions necessary to making a decision about appropriate clinical designs.
Why Should You Attend:
Randomized Control Trials (RCT) aimed at showing superiority remain the gold standard in clinical trial research, but are not appropriate for trials in which the aim is to show that a new treatment is equivalent or at least non-inferior to the current standard of care. The design of non-inferiority (NI) and equivalence trials is not as straightforward as that of the RCT superiority trial, and requires precise definitions of the interval of equivalence and/or region of non-inferiority.
In this session, we will explore the differences among superiority, NI, and equivalence trials, including development of the precise research questions necessary to making a decision about appropriate clinical designs. You will learn how to determine the appropriate interval of equivalence or acceptable “margin” of inferiority and also design appropriate hypothesis tests and their statistical interpretation. We will discuss how bio-creep can occur in NI trials and how you can avoid it. We will also examine details of representative studies and review relevant FDA guidances.
Areas Covered in the Webinar:
- Overview and comparison of NI, equivalence, and superiority study objectives and designs.
- Zeroing in on the specific clinical question to be asked.
- Choosing the appropriate design to answer the specific clinical question.
- How to determine the appropriate interval of equivalence or acceptable “margin” of inferiority.
- Appropriate hypothesis tests and statistical interpretation. (for nonstatisticians)
- Risk of “BioCreep” and other controversies associated with these alternative approaches.
- FDA guidance and CONSORT considerations.
- Time:
- 2:00pm-3:00pm
- Description:
- This webinar on clinical study design will explore the differences among superiority, Non-inferiority (NI), and equivalence trials, including development of the precise research questions necessary to making a decision about appropriate clinical designs.
Why Should You Attend:
Randomized Control Trials (RCT) aimed at showing superiority remain the gold standard in clinical trial research, but are not appropriate for trials in which the aim is to show that a new treatment is equivalent or at least non-inferior to the current standard of care. The design of non-inferiority (NI) and equivalence trials is not as straightforward as that of the RCT superiority trial, and requires precise definitions of the interval of equivalence and/or region of non-inferiority.
In this session, we will explore the differences among superiority, NI, and equivalence trials, including development of the precise research questions necessary to making a decision about appropriate clinical designs. You will learn how to determine the appropriate interval of equivalence or acceptable “margin” of inferiority and also design appropriate hypothesis tests and their statistical interpretation. We will discuss how bio-creep can occur in NI trials and how you can avoid it. We will also examine details of representative studies and review relevant FDA guidances.
Areas Covered in the Webinar:
- Overview and comparison of NI, equivalence, and superiority study objectives and designs.
- Zeroing in on the specific clinical question to be asked.
- Choosing the appropriate design to answer the specific clinical question.
- How to determine the appropriate interval of equivalence or acceptable “margin” of inferiority.
- Appropriate hypothesis tests and statistical interpretation. (for nonstatisticians)
- Risk of “BioCreep” and other controversies associated with these alternative approaches.
- FDA guidance and CONSORT considerations.
- Time:
- 2:00pm-3:00pm
- Description:
- This webinar will help you understand the rationale for Generic Drug Product Development via an ANDA Filing and the potential added value of a Paragraph IV Application, exclusive to the US market.
Why Should You Attend:
The unique market positioning opportunity of a Paragraph IV Application in the US Market allows global Generic Product Manufacturers to develop useful Drug Products (even those with high barriers to entry e.g. transdermals) to offer significant value to patients prior to Branded Patent Expiration on providing a Certification of Non-Infringement and an automatic 30 month stay prior to approval.
This 60-minute webinar will help you understand the rationale for Generic Drug Product Development via an ANDA Filing and the potential added value of a Paragraph IV Application, exclusive to the US Market. The mechanism of a Paragraph IV Filing will be discussed using case studies to demonstrate the creation of value prior to Patent Expiration as a unique opportunity exclusive to the US Market.
Areas Covered in the Webinar:
- Strategic Planning for an ANDA vs Paragraph IV
- Efficient Implementation and Communication with the FDA.
- Content and Format of ANDA’s
- Plan for FDA-Sponsor Meetings
- FDA Expectations and CMC Data including Bioavailability/Bioequivalence
- Outline of Paragraph IV Applications and Case Studies
- Time:
- 2:00pm-3:30pm
- Description:
- This webinar on project management in human resources will focus on key project management skills for the HR professional. You will learn proven, successful techniques for detailed, systematic, team-involved planning and effective implementation.
Why Should You Attend:
You as an HR leader play a major role in shaping your company’s strategy as well as ensuring that the strategy is carried out as planned. While there is much written about the creation of strategy, there is little written about implementation.
In this 90-minute webinar training, we will talk about strategic and effective management and implementation of programs and ways in which you, as an HR professional, can facilitate both in your company. More specifically, this session will focus on how project management is becoming a critical success factor in the overall HR organizational strategy.