- Time:
- 2:00pm-3:30pm
- Description:
- This 90-minute webinar will examine the many myths that get in the way of clinical standards adoption and demonstrate how complying with required standards benefits both the FDA and sponsors.
Why Should You Attend:
Within the next 4 to 8 years, all CROs and sponsors will have to adopt clinical data standards for all studies being submitted to the FDA. While some companies have implemented standards already, many more have not. Designing and implementing the right standards the right way is a significant challenge, and to make matters worse, there are many beliefs about standards that make the task seem even more daunting than it is.
This webinar will help to dispel the myths and common misconceptions surrounding the adoption of clinical data standards and show how the broader the standards implementation across functional areas is, the greater the benefits to both FDA and sponsors.
- Time:
- 4:30pm-5:00pm
- Description:
- Lipid profile, also called as lipid panel or complete cholesterol test is a blood test that can measure the quantity of triglycerides and cholesterol in your blood.Lipid profile can help determine risk of the increase of plaques in arteries that can lead to narrowed or blocked arteries (atherosclerosis). Usually, high cholesterol levels do not cause any signs or symptoms, and thus lipid profile is a key tool. High cholesterol levels often are a major risk factor for heart disease.Join talk by our experts to get an insight into the interpretation of the lipid profile, comprehensive care and pertinent follow up in order to make our lipids our allies.
- 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:
- 11:30pm-11:59pm
- Description:
- Do you feel “blocked” to your intuition?
Do you wish that you had a clearer connection to it and Trusted it?
If you feel this way you are not alone.The simple truth is that everyone has intuition or a 6th sense. Like instinct it’s part of our natural ability to sense beyond our 5 senses. We feel “blocked” to it when something has come up to review or we are not sensitize to it. Everyone at some time or another, even the best psychics feel blocked to their intuition and everyone can improve their connection no matter what level they are at. On this call you will learn 4 common mistakes that people make that “block” their intuition, discover the ways that intuition comes in for you, learn exercises to strengthen your intuition, learn how to trust your intuition and understand how energy work opens your psychic centers. But that’s not all!! Marie will also work with the group as a whole—this includes anybody live or listening for the first time by way of the recording—around energy blockages to higher degrees of intuition. She will tap into the energy of those who have registered for the call and sense what the number 1 issue is of the group and the best way to heal it.
For LIVE participants, Marie will be making a special offer you won't want to miss!
To Register go to:
- Time:
- 12:00am-12:30am
- Description:
- Do you feel “blocked” to your intuition?
Do you wish that you had a clearer connection to it and Trusted it?
If you feel this way you are not alone.The simple truth is that everyone has intuition or a 6th sense. Like instinct it’s part of our natural ability to sense beyond our 5 senses. We feel “blocked” to it when something has come up to review or we are not sensitize to it. Everyone at some time or another, even the best psychics feel blocked to their intuition and everyone can improve their connection no matter what level they are at. On this call you will learn 4 common mistakes that people make that “block” their intuition, discover the ways that intuition comes in for you, learn exercises to strengthen your intuition, learn how to trust your intuition and understand how energy work opens your psychic centers. But that’s not all!! Marie will also work with the group as a whole—this includes anybody live or listening for the first time by way of the recording—around energy blockages to higher degrees of intuition. She will tap into the energy of those who have registered for the call and sense what the number 1 issue is of the group and the best way to heal it.
For LIVE participants, Marie will be making a special offer you won't want to miss!
To Register go to:
- Time:
- 2:00pm-3:00pm
- Description:
- This HIPAA risk analysis webinar will help you to understand the components needed to conduct a comprehensive security, risk analysis for your organization, in order to comply with the HIPAA standards and the far reaching affects of the HITECH Act. You will learn how to identify sources of PHI and ePHI in your organization, external sources and the threats to information system that contain PHI and ePHI.
Why Should You Attend:
This webinar will help you analyze and understand the two very specific HIPAA-security compliance assessments. You will be able to develop organizational compliance plans that address both privacy and security within your organization, specifically addressing your ability to secure patient information within your company, in both physical and electronic forums.
When assessing the risks and vulnerabilities associated with PHI and ePHI, there are three key questions health care organizations should ask, before performing a risk analysis.
1. Can you identify the sources of PHI and ePHI within your organization, including all PHI that you create, receive, maintain or transmit?
2. What are the external sources of PHI/ePHI?
3. What are the human, natural, and environmental threats to information systems that contain PHI and ePHI?
This webinar will not only address answering the above referenced questions, but moreover, this discussion will allow you to put these questions/answers in perspective to address your internal and external security needs and devise the most comprehensive plan for your organization's demands.
- Time:
- 2:00pm-3:00pm
- Description:
- This municipal securities compliance training will clearly explain the MSRB (Municipal Securities Rulemaking Board) Rule-37, discuss the key elements of political contribution restrictions and prohibitions on the municipal securities business, disclosure requirements, violations and how to prevent them.
Why Should You Attend:
The Municipal Securities Rulemaking Board (MSRB) Rule G-37 was enacted to ensure the standards and integrity of the municipal securities industry are maintained and to detect and prevent fraudulent activities and violations. The rule's complexities have caused several firms to violate its requirements, resulting in bans in negotiated and/or financial advisory business as well as payments of very large fines.
This training module draws on the expertise of veteran municipal securities compliance officers with over 40 years combined regulatory experience. In addition to discussing in detail, the elements of political contribution restrictions and prohibitions on the municipal securities business, this course will use real-world case studies to enhance your understanding of the material that can be immediately applied in the workplace. Attendees will learn the disclosure requirements for political contributions in the municipal securities business. The course will also discuss how a ban on the municipal securities business works if a political contribution violation occurs.
Areas Covered in the Seminar:
- Political contribution restrictions.
- How a BAN on the municipal securities business works if a political contribution violation occurs.
- What individuals are covered and require compliance with MSRB Rule G-37.
- Regulatory guidelines on immunogenicity of biologics; FDA, ICH, CHMP, EMEA.
- Prohibition on soliciting and coordinating/bundling political contributions.
- Prohibited from circumvention the Rule.
- Indirect contribution.
- Political party payments.
- Disclosure requirements on political contribution and municipal securities business activities.
- Real-world case studies.
- Time:
- 2:00pm-3:00pm
- Description:
- This FDA GMP training will help you understand the current requirements for raw material management with tips for practical implementation. It covers FDA’s expectations from GMP facilities regarding raw material vendor selection, measures for assuring acceptable quality of material supplied, expectations from quality control and documentation processes, and training requirements, with case studies.
Why Should You Attend:
This webinar is a must for GMP facilities or facilities trying to be GMP compliant irrespective of the kind of product manufactured: drug, biologic, diagnostic kit, medical device or dietary supplements. This presentation will help you understand the current requirements for raw material management with tips about practical implementation. We would discuss the FDA’s expectations from GMP facilities regarding raw material vendor selection, measures for assuring acceptable quality of material supplied, expectations from quality control and documentation processes, and training requirements, with case studies. Attendees will be able to use the training to evaluate existing programs and get tips about assuring compliance with FDA requirements. Impact on compliance with other regulatory requirements in other parts of the World will also be discussed.
- Time:
- 7:00pm-8:15pm
- Description:
- Wish you knew how to consistently attract ALL the new clients you need?
Join us for an informative Webinar...
The Secret to MORE Clients - 5 Powerful Client Getting Strategies
It's on Thursday, March 28th, Noon PST, 3 PM EST, 7 PM GMT
Let's face it. Marketing your business and getting enough clients can be a real challenge - especially in today's marketplace. Perhaps your current marketing activities yield mixed results. You may find it hard to tell exactly what works and what doesn’t, and find it almost impossible to get consistent results!
How would you like to end this vicious cycle of marketing like crazy while still not having enough clients?
Let me show you the way...
For more information and to register for the webinar, please visit
http://www.sueclement.com/ms7.php
I’m Sue Clement, Marketing Strategist and the author of the authoritative guide to getting referrals, "Insider Secrets To Referral Success." I've been helping hundreds of solo entrepreneurs grow their business and get more clients.
I want to show you how to get clients more easily too. You CAN change your results, right now...
Join us for an informative 75-minute webinar filled with actionable ideas you can implement immediately.
You’ll discover...
* The EXACT strategies I use to grow my list and get in front of my ideal prospects – you’ll begin reaching MORE people with LESS effort! (And no, I'm NOT talking about spending scads of dollars to do this).
* How to get more visibility and position yourself as the expert in your field so you'll attract more clients -- the ones that are willing to pay you more!
* My signature success formula to keep your funnel full of ideal pre-sold prospects.
* The missing ingredients that are keeping you in struggle mode never knowing where your next client is coming from.
* How to simplify your marketing so you can focus on reaching your Ideal Clients (this will save you tons of frustration, not to mention hundreds of dollars).
Go ahead and click on the link below to get access to my webinar:
http://www.sueclement.com/ms7.php
- Time:
- 2:00pm-3:15pm
- Description:
- This training on bio-analytical methods validation will help you understand the clear, consistent and compliant approaches for instrumental, ligand binding, and cell based methods. A comparison of EMEA and FDA guidances will be presented.
Why should you Attend:
Bioanalytical method validation includes various procedures that demonstrate that a particular method used for quantitative measurement of analytes in a given biological matrix, such as blood, plasma, serum, or urine, is reliable and reproducible for the intended use. It is essential to employ well-characterized and fully validated bioanalytical methods to yield reliable results which can be satisfactorily interpreted.
This webinar will discuss the best practices of Bioanalytical method validation, including components of a validation, how to include critical reagents comparison, selectivity experiments, assessment of stability. Concept of plate and experiment separation. Importance of communication between the development and the validation labs, accuracy of transfer documents (SOPs). Predicate rules, support of clinical and non clinical sample analysis.
Understand - Is validation a regulated activity? When to pull the trigger for validation? Is a stable label internal standard always the best choice? Importance of suitability testing. Value of including critical reagents testing and suppliers. The limits of an assay and where they come from.
- Time:
- 2:00pm-3:15pm
- Description:
- This DHF regulatory compliance training will discuss the structure of a good Design History File, elements to look for when auditing a DHF and how to address issues. It will provide the information necessary to maintain a good DHF that will help manufacturers during a regulatory compliance audit.
Why Should You Attend:
A Design History File (DHF) is a requirement of QSR 21 CFR Part 820. It is a certainty that in an audit from a regulatory body, information from the DHF will need to be provided. Manufacturer's would be well prepared for audits by regulatory agencies if they know the strengths and weaknesses of their DHF, and remediate as needed, prior to the agency showing up at their doorstep. Virtually every section of the design control requirements specifies information which should be found in the DHF. Manufacturer's need to be aware of what gaps exists between the actual DHF and the FDA's expectation.
This webinar will cover the basics on how to maintain a good design history file that will help a manufacturer in a regulatory compliance audit. The webinar will cover the structure of a DHF and steps to take to ensure that the DHF is completed as the design and development process progresses. Additionally, the DHF needs to be maintained as design changes are performed. Information in the DHF can help facilitate design decisions, which often can affect the safety of the device. The DHF provides the knowledge base needed for the manufacturer to maintain the device. It also provides the secrets to a successful Design Control audit.
Areas Covered in the Seminar:
- DHF structures that work well for audits.
- Documents that should and should not go into a DHF.
- When does a DHF need to be created.
- What to look for when auditing a DHF.
- How to address issues with the DHF.
- The usefulness of the DHF in continuing to maintain the product after launch.
- DHF ownership when third parties are involved.