Health and Medicine

The Conference Series LLC LTD welcomes you to attend the “World Dental Implants and Orthodontics Congress” to be held in Tokyo, Japan from August 17-August 18, 2018 with the theme “Embracing Dental implants and Orthodontics Discovery”. Dental Implants and Orthodontics Conferences have been designed in an interdisciplinary manner with a multitude of tracks to choose from every segment and provides you with a unique opportunity to meet up with peers from both industries belonging to Dentistry.

Why is it important to develop an Effective Near Miss Program? Statistics tell us… that for every 300 near misses there is one serious injury! Near Misses occur frequently and the only difference between a Near Miss and an Actual Accident is luck! For example, if while I am driving I send a text message, and a truck suddenly appears in front of me, what can happen? I look up in the nick of time, slam on the brakes, and just avoid hitting the truck – a near miss. This same scenario can apply and instead of looking up in…

Training Options Duration: 60 Minutes Friday, August 17, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: This workshop will introduce to participants the "why and how" to conduct support groups with Latino immigrant youth who enter the United States by crossing the border. Many, if not most of these immigrants have similar experiences that impact their emotional and behavioral health such as the stressors and/or traumas of their native country to include killings, sexual violence, domestic abuse, the takeover of gang life, extortion, etc. and their arduous journey through Central America, Mexico and crossing the Rio Grande. The…

Training Options Duration: 90 Minutes Friday, August 17, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: The HIPAA Breach Notification Rule has been in effect since 2010 and has been significantly modified in 2013. We will discuss the origins of the rule and how it works, including interactions with other HIPAA rules and penalties for violations. Whenever there may be a privacy issue involving Protected Health Information, there may be a reportable breach under the HIPAA regulations. Not all privacy violations are reportable breaches, though, so it is essential to have a good process for evaluating incidents to…

Description China’s Life Sciences Compliance webinar will discuss the regulatory structure and requirements for compliance against China’s CFDA regulations for Pharmaceuticals, Medical Devices, Biologics and Combination Products. The Chinese government's establishment of a single drug regulatory authority in 2003 (China Food and Drug Administration) was an important step toward foreign access, because it eliminated the conflicting standards that prevailed among provincial government agencies, centralized the Chinese healthcare regulatory system, and made it more transparent to industry partners. The CFDA now oversees all medications. Other former functions of the ministry have been assigned to different government bodies. The most important of…

The Dementia Organizing Committee takes an immense pleasure in inviting you to the eventuality of the 10th World Congress on Dementia and Alzheimer’s Disease for productive interactions and an opportunity to present their work and develop regional collaborations in the field of Dementia Care. Dementia 2018 welcomes all the renowned and aspiring researchers, scientists and business delegates, who are significantly putting their effort to improve the life of population with Dementia. Copenhagen, Denmark will be the significant venue during August 16 to 18, 2018 with the international speakers from different geographical regions to explore the scientific sessions. Scientific sessions of…

Overview: This webinar will cover the key areas of how ICH Q7 was established, it's goals and objectives, expectations of the healthcare authorities involved and practical differences that you will experience in a GMP inspection of a facility by FDA, an EU Competent Authority or PMDA. Why should you Attend: It has often been stated that "FDA inspects for compliance; European inspectors inspect for adequate science". Yet GMPs have been enshrined into law for many countries and a drug/biologic/medical device manufacturer should have a reasonable expectation of all inspections being the same. ICH Q7 was established by US / EU…

This webinar describes the validation planning process with particular emphasis on avoiding six common pitfalls. Increased use of software from 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.” Many companies struggle with understanding how to avoid major mistakes when validating software to FDA standards.

Training Options Duration: 60 Minutes Thursday, August 16, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: Practicing medicine is not like other jobs that have a tradition of retirement at age 65. Physician shortages fuel support for physicians seeking to continue their careers indefinitely. Patient safety is paramount, but is it served by applying an age limit to medical staff membership and clinical privileges? If so, what is the magic number? Why should you Attend: Can medical staffs and hospitals place restrictions on physicians based on age? Should hospitals and medical staffs place restrictions on physicians based on…

This three-day course presents major clinical topics in the field of Rheumatology to assist physicians preparing for the American Board of Internal Medicine (ABIM) Subspecialty Examination in Rheumatology. Trainees preparing for their initial board exam - as well as rheumatologists who are candidates for ABIM recertification - are the target audience. The diagnosis and management of difficult and unusual clinical problems will be emphasized; an overview of important advances related to clinical rheumatology will also be included. URLs: Tickets: https://go.evvnt.com/247123-1?pid=154 Inquiries: https://go.evvnt.com/247123-3?pid=154 Time: 07:00 to 13:00 Prices: Recertifying Physicians: USD 750.0, Advanced Practice Health Professionals: USD 650.0, Fellows in training,…

Description The Theory of Lean Documents is the product of applying lean principles to the creation, design, process, and management of controlled documents typically found in regulated industries. Just as lean principles challenge traditional process concepts and "push" systems, many traditional document practices are artifacts of a flawed approach. Lean documents presents a fresh departure from these practices, while building upon proven principles. Lean configuration comes from the same principles, utilizing the unique power of software solutions to take over functions that had previously burdened controlled "paper" documents. Course Objective Do you find yourself constantly struggling to create, manage, and…

Description This webinar will discuss HIPAA audit and enforcement regulations and processes for 2018 and how they apply to covered entities and business associates. Attendees will learn how to prepare for HIPAA audit to avoid fines and penalties for HIPAA violations. Why Should You Attend: This webinar will examine the updated HIPAA Audit Protocol as well as other questionnaires that have been used in the past and may be used to help prepare an organization for a future review. We will present methods for using the contents of the HIPAA Audit Protocol to build your own compliance plan by extracting…

Description This seminar will help you understand in detail Computer System Validation (CSV) and how to apply the System Development Life Cycle (SDLC) Methodology when validating computer systems subject to FDA regulations. This is critical in order to develop the appropriate validation strategy and achieve the thoroughness required to prove that a system does what it purports to do. It also ensures that a system is maintained in a validated state throughout its entire life cycle, from conception through retirement. We will discuss the phases within the SDLC, and how these form the basis for any CSV project. The importance…

Training Options Duration: 60 Minutes Wednesday, August 15, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: Final regulations for the new HIPAA Breach Notification Rule require much more than notifying individuals affected by a Breach of their Protected Health Information (PHI). Covered Entities and Business Associates first must follow and document a very specific process to determine if a Breach occurred. If no Breach occurred documentary proof must be kept for six years. If a Breach did occur timely notifications and other actions must be undertaken and documented. This webinar will explain: What Covered Entities and Business Associates…

Overview: This one-day seminar will be addressing how medical practice managers (or compliance offers) need to get their HIPAA house in order before the imminent audits occur. It will also address major changes under the Omnibus Rule and any other applicable updates for 2018. The primary goal is to ensure everyone is well educated on what is myth and what is reality with this law, as there is so much misleading information regarding the do's and don'ts with HIPAA - I want to add clarity for specific to medical practice managers. We will get into the do's and don'ts relating…

Description This lesson will be going into great detail regarding you practice or business information technology and how it relates to the HIPAA Security Rule, in particular portable devices. Areas covered will be texting, email, encryption, medical messaging, voice data and risk factors as they relate to personal devices. I will uncover myths versus reality as it relates to this very enigmatic law based on over 1000 risk assessments performed as well as years of experience in dealing directly with the Office of Civil Rights HIPAA auditors. I will speak on specific experiences from over 17 years of experience in…

Description Failure Mode and Effect Analysis can be used to assess the efficacy and efficiency of the device in actual use. Failure Mode Effects Analysis (FMEA) can have a number of variations the aim is to thoroughly review what can go wrong in use and what kind of misuses may be made. The device manufacturer must consider how to protect patients in case of misuse of the device such as ventilators and PCA pumps for pain control. Many patients have died from its inadvertent misuse. It is also important to consider processes such as packaging, sterilization, shipping of wrong kits,…

Description Bioassays are used to demonstrate that a biologic product performs per the stated function and potency. Typically, these methods are performed in living systems. Cell-based methods can have inherent variable due to the nature of living systems. Minimizing potential variability can be achieved through careful documentation and analysis of assay performance on control charts. Monitoring numerous parameters may assist laboratory scientists, laboratory managers, QC and QA personnel identify and manage trends that could lead to OOS/OOT results. Since the number of parameters evaluated is dependent on the cell-type, assay-type, and number of critical component or reagents, this webinar will…

Given the excitement and anticipation of increasingly more promising prophylactic treatments and gene therapy, the inaugural Hemophilia Drug Development Summit plays host to the leading pharma and biotech players working to develop longer acting and more efficacious therapies to overcome significant unmet medical need and prevent resistance to factor replacement therapies. Fueled by current investment in the space and novel therapeutic strategies to improve current standard of care, the development of hemophilia therapeutics has been reinvigorated. Touted as an area of large unmet medical need but a well understood and defined disease profile, investment in this space is set to…

Training Options Duration: 60 Minutes Tuesday, August 14, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: Being in compliance with HIPAA involves not only ensuring you provide the appropriate patient rights and controls on your uses and disclosures of protected health information, but you also have the proper policies and procedures in place. If audited or the subject of a compliance review you will be required to show the government you have all the necessary documentation in place for safeguarding patient Protected Health Information and indicate how you addressed all required security safeguards. This starts with the fundamentals…