Health and Medicine

Training Options Duration: 60 Minutes Wednesday, August 8, 2018 | 11:00 AM PDT | 02:00 PM EDT Overview: In this session Mr. Wolfe will provide an overview of the Stark Law and Anti- Kickback Statute.He will also discuss best practices for auditing physician contracts on behalf of health systems, hospitals, medical groups and physician practices. The webinar will focus on regulatory requirements, key provisions, valuation considerations and potential pitfalls that should be avoided. Why should you Attend: This webinar will offer best practices for implementing and auditing physician contracts to minimize liability and penalties. Areas Covered in the Session: Provide…

Cardiology Meetings welcomes you at Cardiology and Healthcare conference going to be held in Abu Dhabi, UAE during August 9-11, 2018 which unites brief keynote presentations, speaker talks, exhibitions, Symposiums, workshops. Cardiology Care 2018 is the Cardiology meetings which will be most visited by all the eminent cardiologists, cardiology educators, postgraduates, affiliations, business meanders under a solitary rooftop. This Cardiology conference will assist to framework organization, B2B teaming up amidst specialists and academicians. Cardiology Conferences promotes awareness against risk factors and advancements about the cardiac care. This cardiology meeting lay a platform for postgraduate education and scientific work in the…

This new 2-day Seminar on Computer Systems Validation will explore proven techniques for reducing costs associated with implementing, using, & maintaining computer systems in regulated environments. The FDA performs GxP & Part 11 inspections, with an updated Annex 11 regulation, & companies must update their systems and processes to maintain compliance. Majority of inspection reports such as 483’s and Warning Letters quote issues with 21 CFR Part 11 and data integrity as deviations from GxP regulations. Only way to control and avoid warning letters is by receiving effective Training. Our presenter’s extensive years of experience in the field of third…

Training Options Duration: 60 Minutes Thursday, August 9, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: HIPAA compliance consists largely of having the right forms and signatures. On the other hand paperwork will not protect you or your patients from the the most common kinds of data breaches. Learn important real world measures dentists should be taking that can make an actual difference in patient data security, including the one and only procedure you need to protect your practice from data breach (your "get out of jail free" card). This is an entertaining, must see presentation from Dr.…

Training Options Duration: 3 Hours Thursday, August 9, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: This three hour webinar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order as HIPAA is now fully enforced and the government is not using kid gloves any more. It will also address major changes under the Omnibus Rule, Trump administration, and any other applicable updates for 2018 and beyond. There are an enormous amount of issues and risks for covered entities and business associates these days - we will speak to the most…

Description This course offers extensive examination of the FDA’s regulations of biological products such as HCT/Ps from pre-clinical testing to post-marketing regulatory requirements. Specific ethical and regulatory considerations will be discussed for various HCT/Ps. Why Should You Attend: Stem cells have ability to differentiate into numerous cells upon various stimulations. This has led to their wide utilization across several therapeutic areas of medicine, including high risk diseases. Of course, significant scientific breakthroughs in the use of stem cells to prevent, diagnose, and treat numerous diseases has caused numerous start-up companies to form. Despite, such promise, the FDA has yet to…

Why Should You Attend: Analytical methods and procedures should be validated to ensure reliability, consistency and accuracy of analytical data. Compendial methods should be verified to demonstrate the suitability of laboratories to successfully run the method and when methods are transferred between laboratories successful transfer should be demonstrated through testing. In case a laboratory wants to use an alternative method instead of a compendial method, equivalency of the alternative method to the compendial method should to be demonstrated. Method validation recently got highest attention from regulatory agencies and industry task forces. For example, FDA and EMA released guidelines on method…

Description This webinar provides understanding of the requirements for residual solvents addressed in ICH, USP, EP and JP and focus on the recent changes to USP . It will also help attendees utilize strategies to minimize the testing and resources required to meet the requirements. Why Should You Attend: This course focuses on recent changes to USP which can increase flexibility and reduce workload for testing of residual solvents in raw materials and finished products. It addresses options such as whether to test raw materials or drug products, whether to use USP or alternate testing methods, when to screen for…

SAVE $150 Off WCPC with code: EVVNT150* For more than 10 years, physicians, podiatrists, physical therapists, wound care surgeons, nurses, nurse practitioners, physician assistants, dietitians, and other allied and industry professionals have relied on the Wound Certification Preparation Course to improve their knowledge of wound care and prepare for the wound certification board exams (CWCA®, CWS®, or CWSP®). The intensive, two-day event: • Covers the essentials to get wound care-certified • Improves your chances of passing the CWCA®, CWS®, or CWSP® board certification exams • Taught by an interdisciplinary panel of ABWM Certified Wound Specialists • Only course recommended by…

With the pharmaceutical regulatory environment constantly evolving, it is extremely important to always be prepared for an inspection during a clinical trial. As sponsors of clinical trials, pharmaceutical companies are required to ensure GCP guidelines are upheld by implementing inspection readiness. Inspections are a crucial part of clinical trials, and it is extremely important that all companies are ready and properly follow GCP guidelines. Inspections are an ongoing process involving all stakeholders, and the real question is how/what can you do in your organization to reduce the frequency of inspections? By properly preparing for inspections, adopting and understanding all the…

To combat the burden of new regulatory requirements, operational challenges and renewed infrastructure needs, the life science industry must take a holistic and collaborative approach to achieving data disclosure compliance. Through data disclosure and transparency, life science organizations decrease the chances of clinical trial duplication, ensure public understanding and access, and ultimately promote brand integrity. At the 2nd Disclosure and Transparency for Clinical Data Summit, the star-studded speaking faculty will define standardization processes for disclosure and registry, provide best practices to balance commercial confidentiality and public access, and examine proven tactics that preserve data utility while ensuring adequate anonymization. This…

With the support of organizing committee and worldwide organisations, we are having immense pleasure to organize “Annual child and family healthcare nursing conference", August-13-14, 2018 at Bali, Indonesia. We take the privilege to invite participants- speakers, students, delegates and exhibitors from across the globe to its flagship conference Healthcare 2018. Healthcare Conference 2018 will focus on the latest exciting and novel topics in all areas of childcare and family healthcare nursing. It offers an exclusive opportunity for those who are looking to obtain continuing medical grades and those who are willing to share their research expertise to the world. It…

This training program will discuss in detail the CMS requirements for hospitals to help prevent the hospital from being found out of compliance with the grievance regulations. It will also cover a new law under the OCR Section 1557 which requires the hospital to have a new process for handling discrimination complaints.

Training Options Duration: 90 Minutes Monday, August 13, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: This webinar will be addressing the ins and outs of identifying what is and what is not PHI, proper ways to disclose this information, common sense security methods, what we can and can't do under HIPAA relating to disclosures, and how to properly investigate a breach (or a suspected breach). We will also be addressing how practice/business 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…

Course Objective: The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices. Reasons To Attend: Good Laboratory Practices (GLPs), CFR part 58, are a set of guidelines for conducting nonclinical laboratory studies that support or are intended to support applications for research or marketing permits for products such as food and color additives, human and animal drugs, medical devices for human use, biological products and electronic products that are regulated by the FDA. GLPs are not enforceable by law. They do not include manufacturing of product. GLPS are for non-clinical laboratory studies…

Description Email and text message are subject to the HIPAA Security Rule transmission standard. Changes in the Omnibus Rule in 2013 further clarified the importance of proper usage of email and text message, examples of electronic transmission media. Oftentimes used as a method to transmit PHI, electronic transmission media is an area that covered entities need to develop and implement policies and procedures to ensure HIPAA compliance. HHS states 1. Covered entities have a "Duty to Warn" individuals of the risk of unencrypted transmission and that warning is a necessary step in protecting their PHI. 2. Unencrypted email and text…

Description This training program will discuss in detail the CMS requirements for hospitals to help prevent the hospital from being found out of compliance with the grievance regulations. It will also cover a new law under the OCR Section 1557 which requires the hospital to have a new process for handling discrimination complaints. Why Should You Attend: If a CMS surveyor showed up at your hospital tomorrow would you know what to do? Are you sure you are in compliance with the entire grievance requirements by CMS, OCR, and the complaint standards by the Joint Commission or your accreditation organization?…

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…

This medical necessity documentation webinar will cover all the key information needed to support your efforts to document and demonstrate Medical Necessity of services.