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Courses

  • 81 Request Info

    Root Cause Failure Analysis Closed Loop Corrective Action

    Root Cause Failure Analysis is an analytical approach used to identify and solve problems. Analysis is presented in the Seven Basic Tools of Quality in addition to advanced methods used to increase organizations effectiveness, efficiency and reliability.
  • 82 Request Info

    FDA Inspections - Do's and Don'ts 2019

    Overview: In this webinar speaker will define the steps necessary to prepare for an FDA inspection and discuss details surrounding the management of inspections from announcement to close out meeting. Why should you Attend: This session will discuss how to prepare for the inspection, what to do during the inspection and the close-out interview, and how to respond to the inspection.
  • 83 Request Info

    HIPAA 2019 - Staying Competitive and Complying with HIPAA

    HIPAA compliance takes time. But both goals can be accomplished - in fact, a good compliance program can make you even more competitive because compliance helps protect and grow your business and sets you apart from your competitors. For example, knowing how to use social media and electronic communications within HIPAA rules is key to staying competitive.
  • 84 Request Info

    Compliance with the New ICH GCP Revision 2 Addendum

    This webinar will cover these new requirements for running clinical trials, update you on further revisions of ICH GCP R2 and evaluate the changes and discuss how these should have been implemented for sponsors, CROs/vendors and study sites. This will enable you to meet the new international GCP standard to ensure regulatory compliance and the acceptance of clinical trial data by the regulatory authorities internationally.
  • 85 Request Info

    FDA's New Import Program for 2019

    Overview: In this interactive session author will discuss about the FDA's required information for the PREDICT software screening prior to entry and Custom's Harmonized Tariff Schedule (HTS). Why should you Attend: The new import entry filing requirements became effective in 2016 and are posing problems for user. Failure to provide the correct information creates costly delays and, in some cases, the frustrating task of contacting the FDA to resolve the problem.
  • 86 Request Info

    Data Integrity: Compliance with 21 CFR Part 11

    Overview: This webinar describes exactly what is required for compliance with Part 11 and the European equivalent Annex 11 for local, SaaS/Cloud hosted applications. Areas Covered in the Session: What 21 CFR Part 11 means today Purpose of Part 11 What does Part 11 mean? SOPs System features Infrastructure qualification Validation Who Will Benefit: GMP, GCP, GLP, Regulatory Professionals QA/QC IT Auditors Managers and Directors Software Vendors, Hosting Providers
  • 87 Request Info

    How to Implement MDSAP-Requirements into your ISO 13485

    Overview: How a smart implementation of these requirements in the quality management system is possible and finally how the audit for five countries (Australia, Brazil, Canada, Japan, US) is working. Why should you Attend: Your implementation time should be short and need smart ideas to reach the right level to pass the MDSAP - Audit by your audit organization. Areas Covered in the Session: Which Companies must have MDSAP? Which Companies should have MDSAP? Which Companies should postpone MDSAP? What are the requirements of MDSAP?
  • 88 Request Info

    How to Go Global: 5 Proven Foreign Market Entry Techniques

    Due to cost advantages from producing overseas, revenue opportunities from foreign sales and the potential to exploit new technology, tapping international markets holds the greatest potential for growth. The optimal approach for entering or expanding into foreign markets depends on the characteristics and objectives of the particular firm. Proven strategies include exporting, licensing, joint ventures, and establishing an overseas facility.
  • 89 Request Info

    FDAs Quality Metrics - Latest Advances

    Overview: This presentation has been created directly from FDA material, using slides from FDA presentations, both internally to the FDA and to the industry at large. Comments from FDA and industry experts have been captured as well, to provide context and deeper understanding for the trainee. Why should you Attend: This is a very important initiative for the FDA who is planning to use the quality metrics as part of their risk based inspection process. Consequently, putting the quality metrics program in place may reduce the inspection frequency at your facility.
  • 90 Request Info

    How to conduct a Compliance Gap Analysis for ERM

    Overview: This webinar will explain how to conduct a compliance gap analysis for Enterprise Risk Management (ERM). Attendees will learn best practices to ensure ERM compliance. Why should you Attend: Areas of Enterprise Risk Management include: business continuity, disaster recovery, cyber security, information security, emergency management and crisis management. If you are responsible for one of the enterprise risk areas and are not ensuring that the company is compliant, you may be held liable by your corporation.
  • 91 Request Info

    The Value of a Human Factors Program

    Why should you Attend: This year FDA published their priority list for the completion of their Guidance documentation. This annual activity gives us inspection and enforcement insight into the priorities within the agency. Interoperability and Cybersecurity were in the top 3. The implementation of a robust HF program will include both of these disciplines. Following the implementation of the results of a Human Factors/ Usability study, a validation of the safety and effectiveness of the use of the device must be conducted. This webinar will help to sort through the confusion of the standard and help meet regulatory expectations by enumerating the tasks necessary to build a robust Risk based HF program.
  • 92 Request Info

    6-Hour Virtual Seminar on An Integrated Approach to Well-Being at Work

    Employers are getting it - sort of. Most believe in the concept of keeping their employees healthy because it just makes sense. Not only does paying attention to this make a difference in the lives of the people who are the most valuable asset to a company, but there are also many benefits to the bottom line - lowered health claims, improved energy and morale, lowered sickness, and improved productivity. Typical wellness programs may include conducting an annual health fair, inviting a speaker to do the odd lunch n' learn, or even providing gym or fitness subsidies. These initiatives are certainly good starting points, but are they worked into the overall objectives of the organization? Will companies really get the biggest bang for their buck? A one-size fits all program/lunch n' learn/health fair will not have the same effect or return.
  • 93 Request Info

    6-Hour Virtual Seminar on FDA Trends for Computer System Validation

    This webinar will focus on the key areas that are most important for protecting the validity of data that is regulated by FDA, and is typically housed electronically in computer systems. This includes how to properly validate an FDA-regulated computer system in order to ensure security and data integrity objectives are met. Implementing and following the System Development Life Cycle (SDLC) methodology is the best approach for Computer System Validation (CSV) and maintaining the system in a validated state throughout its life.
  • 94 Request Info

    6-Hour Virtual Seminar - Medical Claims Boot Camp - Cracking the Code

    This course is organized into three sections: The life cycle of a claim, coding systems, and reimbursement. Life cycle of a claim Many people understand a portion of the claim adjudication process, but they may not have a complete understanding of all steps necessary to generate and adjudicate claims. We walk through the entire life cycle of a medical claim, from patient registration through provision of services, from claim generation to adjudication, from payment to posting. This is useful for anyone new to the healthcare industry or for persons who want a more complete understanding of the entire claim life cycle.
  • 95 Request Info

    6-Hour Virtual Seminar on Project Management for Non-Project Managers

    This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject. Why you should attend It is not possible to present a complete treatment of project management in the span of 6-hours. It is however, possible to focus in on those most important aspects of project management that are critical to the success of any project. Without basic tools, it is not possible to effectively manage a project to the pre-determined end-date without turmoil and chaos.
  • 96 Request Info

    6-Hour Virtual Seminar a Risk Based Approach to IT Infrastructure Qualification

    GxP Regulated companies are dependent on validated GxP computerized applications to conduct their day to day operations. These applications are, in turn, depended upon a qualified infrastructure that can be relied upon to provide control and regulatory compliance. The consequences of the IT Infrastructure being out of compliance can result in the failure of an entire site or geographic region being brought to a standstill while the compliance issue is resolved. It can also result in regulatory citations during a regulatory inspection as both the infrastructure be out of compliance and also cause the computerized applications that are dependent on it to be out of compliance.
  • 97 Request Info

    Implementing a Compliant Stability Program for Biologics

    Overview: Biologics, as well as small molecule pharmaceutical products, require expiry dating.The complex structure of large molecules presents greater opportunities for degradation. Biologics may lose identity by cleavage ultimately resulting in loss of potency. Also, contamination during processing is a pathway for loss of sterility with a detrimental impact on shelf life. Stability programs for large molecule therapeutics require careful consideration of the factors that can lead to a negative impact on identity, potency, and sterility.
  • 98 Request Info

    Canadian Drug and Health Products Regulatory Landscape

    Overview: The focus will be on drugs, biologics and medical devices, We will also be providing an overview of how the regulatory landscape is currently evolving for most efficient strategic planning. Why should you Attend: This webinar will give you a snap shot of what is current, what is coming and what this means to anyone who is currently developing Drugs and other Health Products for the Canadian market. The focus will be on drugs, biologics and medical devices.
  • 99 Request Info

    Common False Beliefs for Microbial Control and Monitoring

    Overview: It is an unfortunate fact that most water systems today have been designed and are operated and controlled using at least some traditional concepts and methods that are downright wrong. So how could such traditions become so ingrained and be so wrong? How could well-intentioned benchmarking be so misguided? There are many reasons, which will be discussed, but regardless of the causes, we need to be aware of these myths and understand how it really should be done.
  • 100 Request Info

    Dealing with Toxic People

    Overview There are challenges in dealing with people who bring toxicity to the interaction. One challenge is managing the impact it has on us - the other challenge is how to respond effectively - in essence - in ways that continue to allow us to get the job done and maintain a working relationship. In this webinar, you will learn key strategies, tactics and skills to protect your emotional and psychological well-being, while at the same time not letting the other person control or dominate.