- Time:
- 5:00pm-6:00pm
- Description:
- Get on the phone with Business Success Coach, Donna Price, three times per week. Individual coaching 1:1 included in some packages.
For Coaching Packages please go to,
- Time:
- 2:00pm-5:00pm
- Description:
- This OSHA Recordkeeping training will cover critical aspects of OSHA recordkeeping and its requirements, to be compliant with OSHA regulations
Why Should You Attend:
Those responsible for maintaining filling out and recording injuries and illnesses are often confused by what should and should not be included in the OSHA recordkeeping forms. Over-reporting injuries and illnesses can be as serious as under-reporting injuries and illnesses, and can even lead to uncomfortable OSHA inquiries or even inspections. It is also difficult to know how to accurately account for time lost due to injuries and illnesses, especially in the case of a part-time work force. This webinar will help clarify what should be reported as an injury or illness, as well as how to account correctly for lost work time.
Many employers are also confused by which forms should be used to initially report injuries and illness, and those that should be used for submission to OSHA or the proper reporting agency. This session will discuss these and in addition, suggestions will be offered for maintaining confidentiality of the OSHA Injury and Illness data.
Areas Covered in the Seminar:
This seminar will help those tasked with filling out and maintaining OSHA Injury and Illness logs in the following:
- Criteria to use in determining whether and injury or illness should be reported on the OSHA Log.
- Understand the purpose of the OSHA Injury and Illness logs and forms.
- How to calculate lost work days?
- Techniques to assure that the information contained in the logs remains confidential.
- How to calculate injury and illness rates for their workplace?
- Time:
- 2:00pm-3:00pm
- Description:
- This BSA audit training will explain how the best practices in a BSA audit have evolved over the years. It will cover the major components of an effective BSA program that the audit focuses on and the specifics of each area as it pertains to BSA audits.
Why Should You Attend:
Although financial institutions have been managing BSA operations per the regulation requirements, the change in focus to BSA audits has been coming increasingly important. Regulators look to the Bank for assurance and evidence that BSA operations are being appropriately audited to ensure that BSA efforts are appropriately implemented and overseen.
This session highlights BSA audit best practices that are being acknowledged and recognized by regulators and examiners. In this webinar, we will discuss the areas that regulators and examiners are primarily focusing on in regards to BSA audits. The areas of focus outlined in this webinar are based on best industry practices and supervisory experience.
Areas Covered in the Webinar:
- Implementing BSA audit best practices
- Assessing policies and procedures
- Comprehensive Risk Assessment
- Review of monitoring programs
- Determining effectiveness and thoroughness of training programs
- Ensuring qualified employee oversight of daily BSA operations
- Independent testing
- Time:
- 2:00pm-3:00pm
- Description:
- This training will show how you can handle customer complaints in compliance with FDA and ISO Regulations. We will discuss the best ways to document customer feedback, what constitutes a complaint, what do with "non-complaint" feedback, and how to include complaint trending into your firm’s CAPA program.
Why You Should Attend:
Negative customer feedback about a medical device's performance or safety is a strong indicator of whether a firm's manufacturing process is in control. This feedback is therefore subject to many requirements in both the QSR and ISO 13485. Failure to follow up on complaints about medical devices is among the most frequently cited observations on FDA-483s. This session will include the requirements for defining, documenting, and implementing a complaint-handling system, including the requirements for complaint review, investigation, and corrective action, as well as the ISO-specific implications.
This complaint handling webinar session will discuss the best way to document customer feedback, what constitutes a complaint, and what do with "non-complaint" feedback. Also contained will be a suggested method on including complaint trending into your firm's CAPA program. Additionally, the application of risk management to a complaint handling system will be reviewed, and a specific risk management system explained.
Areas Covered in the Seminar:
- FDA and ISO requirements for complaint handling.
- Establishment of complaint handling program.
- What constitutes a complaint.
- ISO-specific implications of complaint handling.
- The roles of investigation and corrective action in complaint handling.
- Complaint trending and reporting.
- Application of risk management to complaint handling program.
- Time:
- 2:00pm-3:30pm
- Description:
- This training on COSO (Committee of Sponsoring Organizations of the Treadway Commission) framework will highlight as well as compare and contrast the critical concepts of two leading compliance documents (COSO 1992 & COSO 2013) that are sure to turn up the heat on management’s efforts related to internal control.
Why Should You Attend:
The new COSO framework will be released in early 2013 and will turn up the focus on how its guidance should be used by companies and auditors when evaluating processes for Sarbanes-Oxley and other control requirements. It is imperative that management, compliance professionals, legal professionals and audit professionals all become intricately familiar with the new COSO framework and the impact it will have on how companies as well as external auditors approach compliance evaluations for not just Sarbanes-Oxley but all regulatory and legislative initiatives. It is also imperative that management learn and accept their critical role as it relates to the management and monitoring of internal controls.
This webinar will focus on the key changes within the COSO 2013 framework and will analyze how this may impact overall compliance efforts. It will explore how COSO 2013 may ultimately impact changes to corporate strategic initiatives and regulatory processes. In addition, it will link the PCAOB’s identified deficiencies of audit firms ICFR to aspects of COSO 2013. Finally, the instructor will discuss the COSO Foundation’s new templates and tools and analyze how these can integrate into your processes.
- 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:
- 4:00pm-5:00pm
- Description:
- Is Your Crack Showing!? Are you investing in your front line leaders to ensure a strong foundation? If not, your leadership cracks could be showing! Find out how to fill these cracks and build a powerful program to prepare your front line leaders for success. Complimentary Webinar: http://bit.ly/Z3VAEd
- 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-3:30pm
- Description:
- This training will discuss regulatory requirements for monitoring of pharmaceutical impurities. It will explain how to monitor impurities in pharmaceutical products as per ICH Q3 A/B requirements and to measure the thresholds to report for regulatory submission.
Why Should You Attend:
Monitoring impurities is considered a critical activity of analytical development in order to ensure the quality of the pharmaceutical products. Current ICH Guidelines indicate that the measurement of impurities should always be conducted for active pharmaceutical ingredient (API) and its drug products. This session will discuss the requirements of ICH Q3A/B for monitoring impurities in API and drug products, practical considerations when examine impurities, how they are reported in regulatory documentation, and key factors to consider when setting impurity specifications.
Learning Objectives:
Upon completion of this session, attendees will understand regulatory requirements in the monitoring of pharmaceutical impurities. Participants will gain practical knowledge about key considerations when reporting impurities for regulatory submission. This session will also discuss observations and infractions that were obtained due to recoding impurities in pharmaceutical labs.
Areas Covered in the Seminar:
- Understand regulatory expectations.
- Discuss warning letters and citations.
- Understand regulatory requirement guidelines surrounding impurities in API and Drug Products.
- Review ICH Q3A for controlling impurities in API and Q3B for impurities in Drug Products.
- Understand different thresholds to report for regulatory submission.
- Time:
- 2:00pm-3:00pm
- Description:
- This training on preserving fish will discuss fish smoking and curing techniques, the methods and its benefits. It covers health risks and HACCP requirements for smoking and curing fish commercially. It will also cover packaging, storage and transportation requirements for mass produced cured fish.
Why Should You Attend:
Modern freezing and canning methods have largely replaced older methods of food preservation but smoking and curing fish still continue. This online training will focus on different techniques of fish curing and smoking commercially. It will explain the benefits and health risks of consuming a smoked or cured fish and the HACCP (Hazard Analysis Critical Control Points) for cured and smoked fish. This online training will familiarize attendees with the packaging of smoked salmon, cod, and other types of fish and additives used in mass commercial packaging of cured fish. It will also cover the shipping and storage considerations for mass produced cured fish.
The instructor will be presenting this session in practical language understandable by all technically educated or trained individuals, regardless of specialty in fish canneries, seafood production plant and other fish processing plants.
Areas Covered in the Seminar:
This Online training on Fish smoking and Curing methods will discuss the following topics:
- Techniques and methods of smoking and curing fish commercially
- Benefits and health risks of curing and smoking fish
- Types of wood burned to add antioxidant and antimicrobial protection
- HACCP (Hazard Analysis Critical Control Points) for smoked fish
- Proper packaging of smoked salmon, cod, and other types of fish
- Nitrate and nitrite additives in mass commercial packaging
- Time:
- 3:30pm-4:00pm
- Description:
- An inguinal hernia in newborns and children is due to weakness in the abdominal wall which is present at birth. Sometimes inguinal hernias do not show any symptoms. Some hernias may be visible when an infant is coughing, crying or straining in the course of bowel movement. The risk of inguinal hernia increases if your close relative, such as parents or sibling, has the condition. Infants who are premature are more likely to develop inguinal hernias. To know more, join our expert talk on Inguinal Hernia in Kids by our Consultant Pediatric and Laparoscopic Surgery, Dr. Rasik Shah.
- Time:
- 2:00pm-3:00pm
- Description:
- This training on managing FDA audits will discuss practical tips to be prepared for an FDA audit of your facility, the appropriate conduct during an audit and the follow-up activities to an audit. You will learn the Do’s and Don’ts of an FDA inspection to ensure a successful audit.
Why Should You Attend:
If your company is marketing a product or service that is regulated by the FDA, you should be prepared for an FDA audit. If you have never been audited by the FDA or if you were last audited 4-6 years ago, if any product or service you offer has been in the news – positive or negative, or if you are getting ready to submit a clinical trial or marketing approval application, chances are you would get audited by the FDA in the near future. Although different facilities are subject to different regulations, FDA auditors follow some general guidelines that are common across all.
Attend this FDA audit webinar to understand the general rules and know through specific case studies , the common themes and differences across facilities subject to GCP, GMP or GLP regulations. We will also discuss ways to be prepared for an FDA audit, conduct during an audit, and follow-up activities to an audit. It will help you convert an FDA audit into an opportunity to demonstrate high quality products and services, and to increase credibility in the industry for your company.
Learning Objectives:
- GCP/GMP/GLP requirements. Why inspections are conducted and by what statutory authority?
- Reasons for FDA conducting an inspection.
- What to expect from an audit? What is subject to FDA purview and what's off-limits?
- Preparing for the inspection/Audit - What you need to know and do to prepare for, during and even after the inspection, a ctions to be taken upon the investigator's arrival, required documentation, Individual responsibilities for the inspection.
- Do's and don'ts of an FDA audit/Inspection.
- Following up on the audit - What to do next? How to respond to findings and facilitating the documentation and remediation process…and reaching final closure?
- Time:
- 2:00pm-3:00pm
- Description:
- This training will cover FDA requirements for labeling dietary supplements. It will show how you can avoid dietary supplement labeling claims by properly labeling your products for the US market per FDA requirements.
Why Should You Attend:
One of the most common citations made against dietary supplement companies stands in the claims made in labeling and marketing materials. Claims that pass a boundary for treating or mitigating diseases and conditions lead to a “new drug” label and a big regulatory headache.
This session will discuss how dietary supplement companies should label their products for the US market per FDA requirements, considerations to avoid claims, building regulatory compliance into company programs for development and launch of properly labeled dietary supplements. Attend this webinar to learn what claims are permissible, what constitutes a disease or drug claim, the implications of making impermissible claims and how to remedy challenged claims.
- Time:
- 2:00pm-3:15pm
- Description:
- This training will discuss the legal differences between employees and independent contractors and advise you on how to stay compliant with applicable law. You will also learn ways to minimize risk when using independent contractors.
Why Should You Attend:
Failure to comply can be costly and getting the classification between employees and independent contractors right is good policy. The Department of Labor and the IRS appear to be cracking down on employers who characterize persons who are lawfully employees as contractors. Employers who mis-classify could be exposed to significant liability.
This webinar will discuss the IRS’ 11 point test and other criteria used to classify workers and clarify the distinctions between employees and contractors. Also, you will be provided with tools to use in classifying your workers as employees or contractors. It may be particularly helpful for small businesses without HR Departments.
At the end of this session, the speaker will handle your specific questions and address any challenges you have/had in understanding the legal differences between employees and contractors.
Areas covered in this webinar:
- What Statutes are Relevant to Classification?
- The IRS Tests for Classification.
- Statutory Employees?
- What Constitutes Control over Work Sufficient to Make a Worker an Employee?
- Leased Employees and Temporary Employees?
- Drafting Independent Contractor Agreements. Conducting Self-audits.
- Time:
- 2:00pm-3:00pm
- Description:
- This session on conducting effective GMP trainings will cover proven learning techniques for technical and compliance related trainings. It will answer key questions about how to make GMP training sessions more engaging and even fun for the learners in your organization.
Why Should You Attend:
Organizations today are under more pressure to deliver ongoing GMP training to keep their employees current and in some cases certified for their job function. The training programs and their effectiveness have come under increased scrutiny by all regulatory bodies. In most organizations this means more employee time in GMP training. Other types of training like professional development is usually voluntary for the employee, therefore they are willing and eager to attend. GMP training on the other hand is usually mandatory and unfortunately has gained the reputation of being boring (deserved or not) thereby bringing in a hostage mentality from many who attend.
This webinar will help you change your GMP training approach to better engage your learners and improve the transfer of knowledge and skill, resulting in a greater level of training effectiveness. The presentation will help you to:
- Identify the characteristics of today’s adult learners.
- Establish a positive learning climate and increase learner motivation and participation.
- Assess your own learning and training styles and apply the concepts to your training delivery.
- Identify ways to gain, maintain and regain participant attention.
- Find effective learning techniques for technical and compliance related content.
- Time:
- 2:00pm-3:00pm
- Description:
- This webinar will help you understand OSHA’s requirements for preventing accidental release of energy or accidental start-up of equipment. You will learn what documents to have in place, including a written lockout/tagout plan, and how to implement it.
Why Should You Attend:
Due to the significant number of fatalities, injuries, fires, spills/releases, and “near misses” in manufacturing, OSHA requires procedures for isolating energy sources and equipment startup. Due to unauthorized persons trespassing or accidentally accessing the area and multiple employers working on these projects they are a significant target for lawsuits for accidental releases of energy or startups. Plaintiff attorneys target the failure of parties responsible for isolating energy sources and controls. Unfortunately, in most cases defendants were not aware of the OSHA requirements until it is too late. In 2011 lockout/tagout ranked 5th in the most common OSHA citation with 3,756 violations.
This webinar will help you understand OSHA’s requirements for preventing accidental release of energy or accidental start-up of equipment. You will learn what documents to have in place, including a written lockout/tagout plan, and how to implement it.
Learning Objectives:
- Understand OSHA's lockout/tagout requirements.
- There is more to hazardous energy control that locking out breakers.
- Know what documents to have in place.
- Reduce risk of unplanned equipment startups or energy releases.
- Time:
- 5:00pm-7:00pm
- Description:
- Acclaimed weight loss expert Angela Buhri will lead the webinar, 3 Hidden and Overlooked Culprits that Are Standing in Your Way to Lasting Weight Loss, on April 13th at 1pm Eastern Time. To be held online and/or over the phone, it will uncover 3 common culprits behind chronic weight-loss struggles in women and what is called yo-yo dieting syndrome. Participants will learn how to lose weight easily and keep it off by knowing and treating the real causes and culprits of weight loss struggle.
Angela Buhri, a weight loss expert for 30 years, will discuss often unrecognized reasons women gain weight and why weight loss can be hard to impossible regardless of diet. The free webinar will also help see the whole picture for creating a personalized weight loss strategy. Spots are limited. Reservations are open now by filling out the form on the website http://SheSlimFast.com.