- 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-3:10pm
- Description:
- This clinical compliance training will examine how compliance professionals and clinical research professionals can work together in a Community Health System (CHS) setting, get their arms around the risks associated with federal and statutory regulations and manage them effectively.
Why Should You Attend:
Community Health Systems are by nature complex organizations.
This complexity increases daily with current trends as these systems merge, consolidate and expand. Arguably more “open” systems than academic centers, they often host clinical research and research procedures in multiple settings, sometimes without their knowledge.
Complex and risk-laden financial relationships also develop as multiple parties execute contracts that may or may not address or protect the concerns of the CHS. This dramatically increases risk related to the Anti-Kickback Statute, the False Claims Act, HIPAA, Medicare Secondary Payer Rule and the Stark Rule.
This session will examine how compliance professionals and clinical research professionals can work together to get their arms
around these risks and manage them effectively.
Learning Objectives:
At the end of this session, attendees will be able to:
- Distinguish risks peculiar to Community Health Systems engaged in clinical research
- Create a work-list of risk items related to clinical research to investigate and manage effectively
- Develop an approach to clinical research that allows physician/investigators to engage and continue in clinical trials while effectively managing related risks
- Time:
- 2:00pm-3:15pm
- Description:
- This webinar will cover how to handle the investigatory interviews to find out the truth. The session will discuss the difference between misinterpreted recollection vs. purposeful distortion and how to get to the bottom of the situation.
Why Should You Attend:
Employers conduct investigations for a variety of reasons; employee complaints, background checks, allegations of misconduct, losses of various types. The shared primary purpose of these investigations is the same - to find out the true facts of a situation to determine a course of action to take - or to not take.
In these investigations, employers often depend heavily upon employee’s recollections. Most employees will do their best to be forthcoming, and recount truthful and factual information to the best of their abilities. So how do you know when you’ve got all the accurate facts? That all witnesses have been forthcoming? Or haven’t purposefully given misrepresentations of the facts? If you’re talking to someone to find out what they know, that you don’t - how would you know what information if any that a witness distorted, left out or used to purposefully misinform? How is an investigator to know the difference between someone’s inaccurate recollections vs. purposeful misrepresentation?
By attending this webinar you will be able to understand the aforementioned and handle the investigatory interviews.
Areas Covered in the Webinar:
- How to tell the difference between misinterpreted recollections vs. purposeful distortion or even providing misinformation.
- Telling the difference between a witness’s selective memories vs. human forgetfulness.
- Finding out if the investigator didn’t ask an understandable, good question vs. a witness’s purposeful omission.
- How to start an interview so most witnesses will be truthful and forthcoming from the beginning.
- How to get to facts that were omitted whether purposefully or not.
- Getting to the bottom of inference and untangling the web of deception.
- The best defense is a good offense mindset – Interviewing those who disorder, complicate, blow up and back track.
- Leave the TV shows out - The 5 best ways to tell if someone is lying to you.
- How to ask good questions to get good answers.
- Time:
- 2:00pm-3:30pm
- Description:
- This OSHA inspection webinar will cover aspects of an OSHA inspection from how establishments are targeted, how to limit the scope of an inspection or investigation, how not to self-incriminate, and when and how to appeal.
Why Should You Attend:
An OSHA inspection can be a costly and disruptive experience for any employer, especially if that employer has not dealt with the Agency, does not have an in-house safety professional or attorney. An OSHA inspection that goes badly essentially says the employer has a defective safety program, is not sufficiently focused on the safety and health of its employees, or is willfully or flagrantly exposing its workers to harm.
This OSHA inspection webinar will cover methodology of an OSHA inspection from how establishments are targeted, how to limit the scope of an inspection or investigation, how not to self-incriminate, and when and how to appeal. We will cover the 10 most common mistakes that often lead to bad outcomes in the event of an OSHA inspection. Understanding how to avoid these (mentioned below) pitfalls will result in fewer citations and smaller penalties:
- Not knowing the enforcer and the applicable regulations/standards.
- Not understanding how inspections are targeted.
- Not recognizing that an employer can be liable for a hazard to another employer’s workers.
- Not knowing what to do if an inspection is anticipated.
- Not knowing or understanding the reason or probable cause for the inspection.
- Now knowing how to limit the scope of an inspection.
- Not strategically managing the inspection as to where the inspector goes, what he/she gets to look at, handling employee interviews, etc.
- Not effectively managing documentation requirements and generating incriminating reports that can be requested by OSHA.
- Not knowing what to do when citations are received.
- Not knowing the appeals process and how to defend against a citation.
- 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:
- 7:00pm-8:00pm
- Description:
- This free tele-class will be held on Tuesday, July 16th from 3pm to 4pm, EST.
This summer learn how to connect with your body and feel beautiful inside and out. Become comfortable with your body, wherever you are!
This one-hour teleclass will teach you two techniques that will carry you through the summer barbecues, beach parties, pool lounging events and beyond. After this free tele-class you will:
• Maintain control of your eating patterns during any event.
• Feel relaxed with your body, feeling joy plus control when in new environments.
• NOT go home feeling guilty.
• Discover how to defeat your stress patterns during the summer
No need to ever worry about sabotaging you and your body. This is a time to relax and enjoy the slower summer months. Bring your body along for the ride with confidence and lightness.
ENJOY the summer with a smile and be in control of your eating habits with a healthy lifestyle that is easy to maintain.
866-762-6224
- 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:
- 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-3:00pm
- Description:
- This webinar on international product registrations will discuss how to develop a plan, implement medical device and pharmaceutical registrations in a timely, efficient manner to help reduce your company's time to market. Best practices in document legalization will be covered too.
Why Should You Attend:
International product registration has changed with the advent of new regulations across the globe. Requirements have changed, more documentation is needed in some cases. In Hague convention member states and non-Hague member states, companies can lose revenue simply by not having the right legalized documents.
The process for approval or clearance of devices outside the USA varies from regulatory body to regulatory body. In some cases, products achieve regulatory approval in an efficient and timely manner. In others, including the US FDA, companies may face a protracted and delayed approval process. Furthermore, recent scrutiny by US regulators and legal authorities is making it more uncertain for companies attempting to gain market access in foreign countries.
This training will provide a guide to facilitate international registrations and reduce time to market by two months. Learning the relevant regulatory requirements and the appropriate document legalization path will speed up the pathway.
Learning Objectives:
Participants in this class will learn how to develop a plan, implement product registrations in a timely, efficient manner to help reduce their companies time to market.
- Time:
- 8:00pm-9:00pm
- Description:
- Register now to learn: How the consumer has changed the way they buy and how selling is adapting to these changes How this has impacted marketing The need for schema cracking ideas – what this means and how it works – Dove example What thought leadership is and what it isn't - a few definitions How and where to start on your thought leadership journey The importance of the right culture to stimulate and promote thought leadership Why content is so important in lead nurturing and lead generation; the difference between content and thought leadership content
- Description:
- Experience the Rollins MBA from the convenience of your home or workplace. Interact online with staff and learn how the Rollins MBA can prepare you to take control of your career.
Time: 9 a.m. or 1 p.m. EST (Each session is 30 minutes.)
- Time:
- 2:00pm-3:00pm
- Description:
- This webinar will provide a comprehensive overview of FDA regulations for cosmetic products. It will help you understand how to be compliant in manufacturing, labeling and advertising of cosmetic products, and thereby ensure successful FDA and state inspections.
Why Should You Attend:
This presentation will help the management and staff of cosmetics companies to understand the regulations and how they apply to their products. We will help you gain a strong understanding of what is involved in becoming compliant in manufacturing, labeling and advertising of cosmetic products. Attendees will learn the importance of documenting and following up on consumer complaints, the marketing errors to avoid, the value of tracking lots, maintaining retention samples, having a quarantine area and its purpose, the necessity in using good manufacturing practices (GMP) in the manufacturing of cosmetics and the possibility of needing a quality testing program.
This session will include the key principles of GMP as defined by FDA as well as incorporate FDA regulatory inspection strategy to identify areas of common deficiency.
Areas Covered in the Seminar:
- Differences between drugs and cosmetics.
- Good Manufacturing Practice (GMP).
- Role of quality Assurance in the manufacturing process.
- Responsibilities of management in FDA compliance.
- Education of employees on GMPs and complaint handling.
- Activities that are common to manufacturing processes.
- State Health Departments and their relationship with FDA.
- Case study on the manufacture of a cosmetic from raw materials to sale.
- Time:
- 6:00pm-7:30pm
- Description:
- Are you a coach, consultant, speaker, trainer, author, or other expert looking to grow your income and influence? The opportunity to get paid handsomely for your expertise while impacting others is not only within your reach right now — it’s also a lot closer than you think.
For one-time only, Angelique Rewers, known by many as "The Corporate Agent," is offering a complimentary LIVE tele-seminar to show you how to target the thousands of REAL companies (with REAL budgets) who are looking for experts just like you RIGHT NOW.
You’ll discover how you can add an additional 6-figures-plus in income a year to your business… AND reach hundreds or even thousands of people with your message. Plus, you’ll learn exactly what you can do to get these high-paying clients to CONTINUE to invest with you at a level you may not have believed possible.
“How to Quickly & Easily Add an Extra 6-Figures (or More) a Year to Your Business By Speaking to Corporate Audiences!”
Thursday, July 18, 2013
2:00 PM Eastern Time
11:00 AM Pacific Time
==> Register NOW at: http://www.thecorporateagent.com/add6figures/
- Time:
- 2:00pm-3:30pm
- Description:
- This training on OSHA workplace electrical safety requirements will provide an overview of the application and requirements of 29 CFR 1910 Subpart S. It will discuss the electrical safety topics that have been interpreted and reviewed in OSHA letters of interpretation.
Why Should You Attend:
OSHA Electrical Safety (29 CFR 1910 Subpart S) requirements are gaining increased visibility in today’s workplace.
The course module will examine the basics of implementing Federal OSHA electrical safe work requirements. It will review the applicability of the National Fire Protection Association (NFPA) consensus standard Electrical Safety in the Workplace, NFPA 70E and survey priority topics of implementation. It will also discuss OSHA formal letters of interpretation and will provide an overview of the content of NFPA70E (2012) specifically examining the concept of approach boundaries and their relationship to hazard assessment and requirements for personal protective equipment (PPE).
Learning objectives:
At the conclusion of the module, students should be able to:
- Define electrically energized work and an electrical exposure.
- Understand in general terms Subpart S and NFPA70E (2012).
- Gain familiarity with key implementation topics such as electrical testing and work, permit requirements, safe approach boundaries, arc flash calculations and required personal protective equipment.
Areas Covered in the Webinar:
- Federal OSHA Electrical Safety (29 CFR 1910 Subpart S)
- National Fire Protection Association (NFPA), NFPA70E
- Time:
- 2:00pm-3:00pm
- Description:
- This clinical compliance webinar will discuss the elements of a Trial Master File (TMF) and show how to set-up and maintain the TMF to ensure it can pass inspection by a clinical trial monitor or auditor.
Why Should You Attend:
- How would you handle missing elements of a regulatory file?
- Who is responsible for which essential elements in a TMF?
- How do you handle versioning of protocols in a TMF?
This course will go over the essential documents which make up the Trial Master File. The presenter will help you understand the fundamentals of the set-up and maintenance of the TMF so you can ensure that when a monitor or auditor visits, the appropriate documentation will be easily located and you will be assured that you have all the documentation required.
Areas Covered in the Webinar:
- ICH guidelines and Good Clinical Practice (GCP)
- Organization of the TMF
- How to write good Memos for TMF
- Versioning in a TMF
- Access and control of the TMF
- Staff responsibilities of the TMF
- Long term storage of the TMF