- 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-3:30pm
- Description:
- This webinar on FDA social media regulations will discuss the best practices utilized by medical device, drug and other FDA and FTC regulated industries when using social media channels, i.e., Web 2.0, like Facebook, Twitter, YouTube and LinkedIn to promote products.
Why Should You Attend:
This webinar will discuss ways manufacturers of life science products are currently using social media in light of applicable laws and regulations, and recent FDA enforcement actions. Practical real-world examples and experiences will be offered. This webinar will also cover new guidance from FDA regarding how to respond to unsolicited requests for off-label information in social media outlets.
Areas Covered in the Seminar:
PROMOTION AND ADVERTISING
- How do FDA and FTC regulations govern social media?
- How is Web 2.0 advertising and promotion different than more standard channels like print, TV and radio?
- What is the current regulatory environment like?
- Are you meeting the FDA guidance, “Responding to Unsolicited Requests for Off-Label Information About Prescription Drugs and Medical Devices”?
FDA COMPLIANCE AND ENFORCEMENT
- If you are using social media improperly, then you are probably violating FDA and/or FTC laws and regulations. How do you go about remedying such issues?
- what is your exposure? The government does not care if “everyone else is doing it.” If you are violating the law, sooner or later, FDA will come knocking.
- Time:
- 2:00pm-3:00pm
- Description:
- This laboratory compliance training will explain how to qualify and validate vendors for reagents in a GLP/GMP laboratory.
Why Should You Attend:
This virtual training will teach you what to look for in vendors, from the necessary standards they should be able to manufacture at to the data they should be able to send with their reagents to pit falls that belie issues with many common reagents. Then, you will learn to validate if the reagents work according to specifications and are suitable for use. Also, you will learn how to manage vendor relationships for the maximum benefit of your laboratory, since relying on one sole vendor can be risky for laboratory needs.
Areas Covered in the Webinar:
The webinar will include the following critical information you will need:
1. How to select vendors for reagents?
2. What does the reagent vendor have to be capable of doing in order to be - suitable for usage in a GLP/GMP laboratory?
3. How and when to be flexible with vendor requirements, and what steps need to be taken in order to allow for flexibility?
4. What information needs to be provided in order for reagent validation to begin?
5. What kind of work needs to be done to validate the reagents for a vendor?
6. How to prioritize and manage vendor relationships to meet key business needs?
- Time:
- 5:00pm-6:00pm
- Description:
- This free tele-class takes place on Tuesday, June 25th at 1pm Eastern
Discover the gap between you and exercise (and exactly how to bridge that gap so that you conquer the “e” word once and for all). This is exactly what you will discover on this call.
It’s time for “your body, your way”.
We’ll discover, together:
--How to befriend your body and achieve freedom from the "e" word
--How to naturally incorporate exercise into your pre-existing lifestyle
My classes are based on sharing, interaction AND information that you can use IMMEDIATELY after the call is over.
How to jump start your metabolism (in the morning, evening or anytime in between)
You’ll come away with information you can use immediately in your life.
Join us June 25 at 1pm EST
- 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:
- 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 corporate ethics and compliance training will provide you simple, but powerful, tools to evaluate your organization’s ethics and compliance program effectively. It will help you understand the importance and role of periodic evaluation in order to ensure compliance and avoid lawsuits.
Why Should You Attend:
The evaluation of an ethics and compliance program for effectiveness is a critical component of understanding whether your program actually has a positive effect on your company in terms of culture and risk management. It is also a critical component of a defensible program should your company be investigated or prosecuted for potential wrongdoing. In both instances – the positive culture and the defensible position – evaluating your ethics and compliance program periodically for effectiveness is not only an increasingly required part of doing business, it will also allow you, your colleagues, your executive leadership and your board to sleep better at night.
This webinar will provide a holistic review and assessment of:
1. the essential ingredients of an effective global ethics and compliance program
2. what tactical steps and substantive issues are of utmost importance in achieving an effective ethics and compliance program
3. what the government’s expectations are with regard to what an effective program means
4. how to test whether your overall program is effective
5. how to maintain and reboot your program for effectiveness
By reviewing the key elements that can make a program effective, this webinar will better equip the attendees with a more comprehensive understanding of the full importance of an effective ethics and compliance program – a real program as opposed to a paper one.
- Time:
- 2:00pm-3:00pm
- Description:
- This Foreign corrupt Practices Act (FCPA) compliance training will discuss common red flags for potential breaches of the Act and recent enforcement trends for noncompliance.
Why Should You Attend:
The Foreign Corrupt Practices Act is seeing increasing enforcement actions that result in significant penalties and reputational damage. Similar legislation is being enacted in multiple countries. Operating in the global arena requires knowledge of this important legislation and others like it.
This webinar will discuss red flags for potential breaches of the FCPA and study recent enforcement trends. Attendees will be able to assess whether their accounting records can form a basis for defense and identify issues. It will also help attendees understand how employees need to be made aware of the consequences of their actions when conducting business in the global markets.
Areas Covered in the Webinar:
- Red flags for potential breaches
- Recent enforcement actions
- Organizational and personal exposure
- Fines and penalties
- What the law actually says
- United Nations Convention Against Corruption
- Time:
- 2:00pm
- Description:
- This OSHA Recordkeeping training will address the key concepts in understanding the OSHA recordkeeping analysis through recent OSHA Interpretation Letters. This training will include hypothetical fact scenarios that present common recordkeeping issues encountered by facility record keepers.
Why Should You Attend:
OSHA injury and illness recordkeeping compliance is a point of emphasis for OSHA, and the recordkeeping regulations are frequently cited by the Agency.
This course will cover the OSHA recordkeeping analysis as explained through recent OSHA Interpretation Letters. While many OSHA Interpretation Letters are published and available on the OSHA website, there are many other unpublished letters that also provide useful guidance explaining how OSHA interprets its recordkeeping regulations. This course will help to prepare you for an OSHA recordkeeping inspection.
Areas Covered in the Seminar:
- The Scope of Work Relationship – differences between OSHA and Workers’ Compensation definitions.
- Understanding the key exceptions to the work relationship.
- Rules for temporary workers.
- The role of employee fault.
- What OSHA means by “restricted work.”.
- The meaning of “significant aggravation.”
- The effect of post-accident drug tests.
- The conflicting doctor rule.
- The nuts and bolts of completing the OSHA 300 Log.
- Completing the 300A Annual Summary.
- Time:
- 5:00pm-6:00pm
- Description:
- - Are you planning to create a mobile application?
- Do you have the necessary resources within your company to create the right mobile app?
- Are you looking for outsourcing partners to help you make your mobile app a reality?
Accelerating Mobile App Delivery:
Meet The Nearshore Mexican Mobile Experts
Free Webinar: Wednesday 26th, 12pm Central, 1pm East
Join Guillermo Ortega, Chief Operating Officer, and David Sandoval, Marketing Manager, share how you can create fantastic mobile applications faster and at lower costs without compromising on time and resources while avoiding complex communication issues.
Who should watch this webinar?
Business and IT Professionals developing or wish to develop a mobile or web application faster and at lowers costs. Companies who are having troubles finding the right development talent for their mobile or web app projects.
Register to learn:
- How you can get the mobile app you want faster
- Nearshore outsourcing benefits for your business
- How to get the right extended team on site or off site
- How to get the most out of your budget
- Meet the iTexico Mexican Team!
- Time:
- 6:00pm-7:00pm
- Description:
- Do you provide continuing education for your clients, association members, or professional affinity groups? Webinars are an effective and flexible medium for bringing this valuable content to your target audiences around the country or around the world.
Planning and delivering a webinar that achieves its educational goals and satisfies your attendees takes conscientious effort and attention to detail. It doesn’t “just happen!”
Join Ken Molay, president of Webinar Success, for a discussion of best practices associated with continuing education webinars. Ken will combine experiences and lessons taken from commercial industry, membership associations, and professional peer groups to identify strategies and tactics that benefit you and your audiences.
Register now to learn the best way to:
-Craft effective titles and descriptions
-Design content for on-screen vs. handout use
-Work with guest presenters
-Plan audience interactions and polls
-Manage audience questions
-Build a useful post-webinar survey
-Deliver value-added resources for attendees
- Time:
- 2:00pm
- Description:
This 3 hour virtual seminar on Japan regulatory compliance requirements will explain the country's regulations and processes (including clinical trials, filings, etc.) and use real world experiences to show how compliance issues are culturally handled for life science products in Japan.
Why Should You Attend:
If your job responsibilities require you to have knowledge of Japan’s regulatory requirements, ensuring compliance with regulatory filings and overall GCP, GMP and GLP compliance requirements or understand how best to consider Japan into your Global Business Strategy, then you will profit from attending our training.
This 3 hour virtual seminar will help you gain a comprehensive understanding of the Regulatory Structure, Clinical Trial Requirements, Marketing Authorization Procedures, Variations Processing, License Renewals and cultural working aspects within the Regulatory Environment in Japan. It will prepare you for regulatory approval processes, Agency meetings, the complexities of running studies in Japan, the importance of partner selection and will also add the cultural knowledge needed for success. The recent changes made by PMDA to be more sponsor and applicant-friendly will be reviewed. Real world experiences on actual interactions with the Agency since these changes were implemented, will also be discussed.
Agenda: (All time in PDT)
- 10:00 – 11:15 am (Powerpoint presentation; Session I)
- 11:15 – 11:30 am Break
- 11:30 – 12:50 pm (Powerpoint presentation; Session II)
- 12:50 - 1:00 pm (Q&A Session)
- Time:
- 2:00pm-3:30pm
- Description:
- This food safety training will provide a comprehensive understanding of food allergens and the risks involved. You will learn how to control or manage food allergens from development to labeling in a food manufacturing environment.
Why Should You Attend:
Undeclared allergens are a Class I FDA recall. Allergen recalls have risen to the second most frequent FDA recalls since 2010. FSMA gives the FDA increased authority to mandate recalls. Allergen sufferers are also on the rise, especially among children. In fact, almost 40% of children with food allergies have severe reactions to those allergens.
Avoidance is the primary defense for food allergen sufferers. It is the responsibility of the manufacturer to control and properly label food allergens to assist this growing and vulnerable population.
This 90-minute webinar will provide a comprehensive understanding of food allergens and the risks involved. You will learn proven and practical methods/ processes to manage food allergens from development to labeling in a food
manufacturing environment.
Learning Objectives:
- Have an understanding of food allergens and the risks involved
- Familiarize with the knowledge of allergens and their alternatives
- Recognize the presence of allergens through labeling review
- Employ GMPs to prevent cross contamination
- Time:
- 2:00pm-3:30pm
- Description:
- This webinar highlights the principles and techniques for internal control in payroll. After a general placement into the COSO framework, the course operationally covers how payroll processes should be designed for internal controls, the specific internal controls that apply to these area, as well as the levels of attribution and delegation of decision power.
Why Should You Attend:
Internal controls are an important part of corporate risk management. Internal auditors must know in details specific tests of control. They are also a fundamental step in the assessment of control risk in external auditing and for the assessment of the effectiveness of internal control over financial reporting, which is mandatory in certain jurisdictions like the U.S.
Even operating managers should know internal controls that apply to the areas under their supervision to avoid unintentional consequences of inappropriate procedures and to protect against wrongdoing by others.
At the end of the webinar speaker will handle your specific questions related to the topic.
Areas Covered in the Webinar:
With reference to payroll:
- Placement within the COSO framework
- Internal control objectives
- Internal control responsibilities within the organization
- Management authorizations
- Matching of financial statement assertions with internal controls
- Process workflows enabled for internal control
- Internal controls and check lists
- Implication of computer systems on internal controls
- Time:
- 2:00pm-3:00pm
- Description:
- This dietary supplements quality compliance training will review the FDA regulatory requirements for manufacturing and commercialization of dietary supplements. You will gain a complete understanding of FDA requirements for manufacturing of nutraceuticals, food drugs, and dietary supplements.
Why Should You Attend:
Do you have responsibility the manufacturing or distribution of a dietary supplement, nutraceutical, or food drug? Are you considering launching a product into this rapidly growing market? Do you provide contract manufacturing capabilities for pharmaceuticals and want to learn more about dietary supplement GMP requirements?
If yes, you should consider attending this one-hour webinar which will educate you on the regulatory and quality compliance requirements for these products.
This session will review FDA regulatory requirements, review 21CFR part 111 covering dietary supplements, analyze applicable regulatory guidance documents, and highlight the increasing warning letter trend from FDA for dietary supplement manufacturers.
Learning Objective:
At the end of this webinar, participants will understand regulatory and quality compliance requirements for dietary supplements (often called food drugs, nutraceuticals, etc.)
Areas Covered in The Webinar:
- Review of FDA regulations in this area.
- History of Dietary Supplement Health and Education Act.
- Review 21CFR part 111 requirements.
- Review applicable FDA guidance documents.
- Overview the key elements of the quality system dietary supplement companies should implement to be GMP compliant.
- Analysis of Warning Letter trends among dietary supplement manufacturers.
- Time:
- 2:00pm-3:00pm
- Description:
- This FDA Software Validation and Verification training/webinar will review the validation planning process with particular emphasis on avoiding six common pitfalls.
Why Should You Attend:
- FDA inspectors are now being trained to evaluate software validation practices.
- Increasing use of automated manufacturing and quality systems means increased exposure.
- Most recalls can be traced back to computerized equipment, exposing the validation process to scrutiny.
- Corporate uncertainty leads to inaction and 'wheel spinning'.
- A third of recent warning letters included citations with respect to improper or ineffective validation.
Many companies struggle with understanding how to avoid major mistakes when validating software to FDA standards. This presentation will review the validation planning process with particular emphasis on avoiding six common pitfalls. The attendee should leave the presentation confident in their ability to improve the level of validation success.
Areas Covered in the Seminar:
- Outline of FDA regulations as applied to software.
- Review of FDA software validation requirements.
- Why validation makes good business sense.
- The 6 Most Common Problems in FDA Software Validation & Verification.
- Strategies on how to avoid the most common problems.
- Advice on successful validation project staffing.
- Time:
- 2:00pm-3:00pm
- Description:
- This U.S. Customs & Border Protection (CBP) compliance training will help you understand best practices when importing products into the U.S.
Why Should You Attend:
If you import merchandise into the U.S., you may not realize, but, you are the responsible party! In this presentation, we will discuss how to comply with U.S. Customs and Border Protection’s (CBP) vast laws and regulations. By the end of the Seminar you will know and understand the importance of tariff classification, Customs valuation, Country of origin marking, intellectual property rights and Free Trade Agreements. You will also learn basic customs concepts and terms like CBP Form 3461 & CBP 7501, Protests, Seizure cases, Liquidated damage claims, Penalties/Fines, Prior disclosure, and FP&F Petition Process.
Learn key best practices and hear real life case studies. Learn what to do, and more importantly, what NOT to do, and what the consequences are for non compliance. The speaker will also share with you the Top 10 Tips When Importing to Ensure Compliance.
Areas Covered in the Webinar:
- Importance of CBP Rulings for Classification, Valuation and Country of Origin
- Cost Savings practices like utilizing Free Trade Agreements
- Importance of protecting Intellectual Property Rights
- Basic customs concepts and terms
- What to do if you encounter a CBP detention and/or seizure case
- Learn when to submit a Prior Disclosure to CBP
- Top 10 Tips When Importing to Ensure Compliance
- Time:
- 6:00pm-7:00pm
- Description:
- Did you know that people watch 20 million hours of video every day on YouTube? Or that social media is a clever and inexpensive way to promote your videos and take them viral? You'll learn how to GROW your business, increase inbound LEADS and improve your brand AWARENESS with your new video marketing strategy ... inexpensively, and while having lots of fun!
- Time:
- 7:00pm-8:00pm
- Description:
- Come join me on this Live webinar to learn my #1 Tip for marketing your business, getting clients & bringing home the bacon! :-) Find out how to make your marketing work, what most people are doing wrong that is killing their businesses & how you can make 1 tiny shift that could change everything.
- Time:
- 7:00pm-8:00pm
- Description:
- Come join me on this Live webinar to learn my #1 Tip for marketing your business, getting clients & bringing home the bacon! :-) Find out how to make your marketing work, what most people are doing wrong that is killing their businesses & how you can make 1 tiny shift that could change everything.
- Time:
- 2:00pm-3:00pm
- Description:
- This 60 minute webinar on how to deal with psychiatric disabilities at work addresses w.r.t. both the legal and psychological issues that often arise. The session covers confidentiality, fitness for duty evaluations, when and why to drug test, the relationship between conduct problems and mental illness, and how to directly address mental health problems with managers and employees.
Why Should You Attend:
The recent amendments to the A.D.A. have a significant impact on the rights of mentally employees as well as the responsibilities of employers. To make matters more confusing, the A.D.A., the F.M.L.A., and worker’s comp can intersect, or supersede, each other when it comes to dealing with psychiatric disabilities.
This webinar will help HR professionals understand how to navigate the difficult and often murky challenge of dealing with \"invisible disabilities.\" To make matters more confusing, the recent amendments to the A.D.A. have a significant impact on the rights of mentally ill employees as well as the responsibilities of employers.
At the end of this webinar the speaker will handle your specific questions related to the topic.
Areas Covered in the Webinar:
- When do conduct problems become mental illness?
- What do you say to a depressed employee?
- What protection do alcoholics and substance abusers have under the A.D.A.?
- How do you handle threats and other disruptive behavior?
- How do you avoid the 5 biggest mistakes managers make in managing mentally ill employees?
- What do you do when an employee talks of suicide?
- How do you handle an employee who comes back from rehab?