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- Description:
- Viraltag is hosting a free webinar this Wednesday, March 23, at 3pm EST. Social media marketing and SEO expert, Sujan Patel, is sharing his strategies for how businesses can drive more ROI from social media. Click to attend live or receive a recording later.
- 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:
- 11:00pm-12:00am
- Description:
- Learn new skills to master the various challenges associated with living with a chronic medical condition. Learn how to take charge of your healthcare and self-care. Discover new ways to give your life meaning and purpose, and explore how to best adapt to changes and losses.
This webinar series provides the road map that will guide you in how to increase wellbeing despite health challenges. By engaging in the mindfulness-based practices presented in these webinars, which were developed out of new advances in psychology, you will learn that the power to be the master of your condition and your life is in your own hands.
Each chapter focuses on a tool to cultivate wellbeing and ends with helpful hints on medical self-efficacy.
This educational webinar series will inform you of evidence-based tools developed from recent advances in psychology. To increase mastery wellbeing, self-care & your ability to work collaboratively & proactively with yon partnership with your doctors.
- Time:
- 12:30pm
- Description:
- You will discover:
• How to create your podcast (in less than 3 minutes!)
• The best podcasting equipment (for every budget)
• The top 5 growth strategies for your podcast
• The top 5 ways to monetize major money with real life examples
Join us 15 minutes early (we'll send you a reminder email) so Wendy can say "hi!" and answer any questions you may have.
After registering, you will receive a confirmation email containing information about joining the webinar.
- Time:
- 5:00pm-6:00pm
- Description:
- DESCRIPTION
Conducting formal Pharmaceutical and Biological Investigations requires insight into the area of concern, the factors which lead to the event and assigning the appropriate personnel to effectively identify Root Cause. The training will provide a stepped approach to the investigative process by looking at: Why the event occurred, Who contributed to the event, Who should lead the investigation, How the event will be resolved and How the event will be tracked for efficacy.
Why should you attend :
The training will provide a sensible approach on conducting investigations within a Pharmaceutical Environment, based upon recent industry experience with companies under FDA Warning Letter oversight. The training will provide the novice and lead investigator with insight on assigning the correct people to the investigation and a methodical approach to the investigative process.
Areas Covered in the Session:
Investigating Non-Conforming Events in Manufacturing and Quality
Root Cause Analysis and Assignment
Identifying Investigators
Investigation Mapping
Determining Efficacy of Investigations
Who will benefit: (Titles)
Quality Assurance Managers (Investigations)
Lead and Associate Investigators
Manufacturing and Quality Personnel Required to Participate in Investigations
Webinar includes:
Q/A Session with the Expert to ask your question
PDF print only copy of PowerPoint slides
60 Minutes Live Presentation
Certificate of attendance
For Registration : http://compliance2go.com/product/?topic=export-documentation
Note: Use coupon code < T9AIO8AY> and get 15% off on registration.
- Time:
- 5:00pm-6:00pm
- Description:
- DESCRIPTION
This webinar is intended to provide practical and actionable information and guidance on how to proactively prepare for a sustainable FDA inspection and to better manage FDA inspection processes including key points of consideration.
This webinar is further intended to discuss and understand FDA’s inspection authority, compliance programs and Agency’s change in inspection policy.
This presentation will greatly help industry better understand the FDA inspection processes with increased awareness.
As a result, you will plan and execute your FDA inspection preparation and management differently in a way to bring more values to your organization – saving a significant amount of time and resources.
Why should you attend :
This webinar is intended to help you get familiar with how to prepare for and manage an FDA inspection including important points of consideration.
Areas Covered in the Session:
Laws and Regulations
FDA Inspection Authority
FDA Manuals for Inspection
Hosting an FDA Inspection
Inspection Types, Categories and Classification
Inspection Process
FDA Forms 482 and 483
Responding to 483s
Why/How/What to Consider for Inspection Preparation and for Better Management
Common Mistakes and Critical Points of Consideration
Laws and Regulations
FDA Inspection Authority
FDA Manuals for Inspection
Hosting an FDA Inspection
Inspection Types, Categories and Classification
Inspection Process
FDA Forms 482 and 483
Responding to 483s
Why/How/What to Consider for Inspection Preparation and for Better Management
Common Mistakes and Critical Points of Consideration
Speaker’s PASS-IT Recommendations
Who will benefit: (Titles)
CEOs
VPs
Compliance Officers
Attorneys
Regulatory Affairs
Clinical Affairs
Quality Assurance
R&D
Consultants
Contractors/Subcontractors
Anyone Interested in the FDA inspection Processes
Webinar Includes:
Q/A Session with the Expert to ask your question
Copy of PowerPoint slides (PDF print only)
60 Minutes Live Presentation
Certificate of Attendance
For Registration :http://c2gowebinars.com/product/?topic=fda-inspection
Note: Use coupon code < T9AIO8AY> and get 15% off on registration.
- Time:
- 2:00pm-3:00pm
- Description:
- This teleseminar is designed for Moms whose child has left home. This is a time of great change! this Teleseminar will provide support and ideas about how you can use this unique transition to thrive in your personal growth.
- Time:
- 3:30pm-4:30pm
- Description:
- DESCRIPTION
The Trans-Pacific Partnership agreement was reached by the 12 member countries in October 2015. The official text was released to the public in November 2015. The TPP will be the largest trade agreement for the United States and other countries when it is signed and ratified according to the national procedures of the concerned countries. Member countries represent 40% of global trade. According to the U.S. Trade Representative site, the TPP will make it easier for American entrepreneurs, farmers, and small business owners to sell Made-In-America products abroad by eliminating more than 18,000 taxes and other trade barriers on American products across the 11 other countries in the TPP.
Why Should You Attend:
This webinar will provide an introduction into some of the key chapters relating to Customs, trade facilitation, duty reductions, and rules of origin and how they could impact your company. Learn how to find out about duty reductions or eliminations, documentation, and certification requirements. If you import/export in any of the 12 TPP countries (United States, Canada, Mexico, Japan, Chile, Australia, New Zealand, Singapore, Malaysia, Vietnam, Brunei, Peru), this webinar will help you better understand some of the new provisions of the TPP.
Areas Covered in the Session:
Introduction to the Trans-Pacific Partnership Agreement (TPP)
Overview of the chapters in the agreement
Review of key chapters on Customs, Trade Facilitation, and Rules of Origin
Review of duty reductions to imported/exported products in the TPP
Rules of origin necessary to take advantage of the duty reductions
Documentation requirements to qualify goods under the TPP
Resources
Who Will Benefit:
Exporters, Importers, Manufacturers. Departments: Import Compliance, Export Order and Compliance, Accounting, Shipping/Receiving, Sales/Marketing, Engineering/Manufacturing, Contracts, Quality Assurance, and Freight Forwarders/Customhouse Brokers, Consultants, Attorneys.
Webinar includes:
Q/A Session with the Expert to ask your question
PDF print only copy of PowerPoint slides
90 Minutes Live Presentation
Certificate of attendance
For Registration : http://c2gowebinars.com/product/?topic=trans-pacific-partnership
Note: Use coupon code < T9AIO8AY> and get 15% off on registration.