All Conferences

11th International Conference on Humanities, Social Sciences, Business and Education (HSSBE-18) scheduled on May 3-4, 2018 Antalya (Turkey) is for the researchers, social-scientists, scholars, engineers and parctitioners from all around the world to present and share ongoing research activities. All accepted papers of HSSBE-18 will be published in the printed conference proceedings with valid International ISBN number. Each Paper will be assigned unique Digital Object Identifier(DOI) from CROSSREF and the Proceedings of the Conference will be archived in HEAIG's Engineering & Technology Digital Library. The papers can be submitted to Emerging Sources Citation Index [THOMSON REUTERS] OR SCOPUS Indexed journals…

9th International Conference on Disaster Management, Building Design, Materials and Civil Engineering (DBMCE-18) on May 3-4, 2018 at Antalya (Turkey) is aimed for the scientists, scholars, engineers and students from the Universities all around the world and the industry to present ongoing research activities, and hence to foster research relations between the Universities and the industry. The Proceedings of the Conference will be published by UR-CPS (Conference Publishing Services) and will be archived in UR's Engineering & Technology Digital Library. Each Paper will be assigned Digital Object Identifier(DOI) from CROSSREF. The Proceeding will be submitted to ISI Thomson for review…

9th International Conference on Science, Engineering, Technology and Healthcare (SETH-18) May 3-4, 2018 at Antalya (Turkey) is for the scientists, scholars, engineers and students from the Universities all around the world and the industry to present ongoing research activities, and hence to foster research relations between the Universities and the industry. The Proceedings of the Conference will be published by UR-CPS (Conference Publishing Services) and will be archived in UR's Engineering & Technology Digital Library. Each Paper will be assigned Digital Object Identifier(DOI) from CROSSREF. The Proceeding can be submitted to SCOPUS journals for review and indexing. In addition the…

9th International Conference on Chemical, Agriculture, Environment and Natural Sciences (CAENS-18) on May 3-4, 2018 at Antalya (Turkey) is aimed for the scientists, scholars, engineers and students from the Universities all around the world and the industry to present ongoing research activities, and hence to foster research relations between the Universities and the industry. The Proceedings of the Conference will be published by UR-CPS (Conference Publishing Services) and will be archived in UR's Engineering & Technology Digital Library. Each Paper will be assigned Digital Object Identifier(DOI) from CROSSREF. In addition the proceedings will be indexed at Google and Google Scholar…

Organizations representing petrochemicals, pipelines, producers, traders, brokers, risk managers, analysts, government, banks and many others will attend to hear the latest developments on the market. Network and do business at the premier event designed for Canadian NGLs and Petrochemicals. Price Pre-Registration Discount (Now-February 23): CAD 1495 Early Registration Discount (February 24-March 23): CAD 1795 Standard Registration (After March 23): CAD 2095 Time: 9:00 am to 12:30 pm Category: Conferences

The importance of 'Creative Operations'- the tools, systems and methods that maximize productivity in the creative process - is being increasingly recognized by leading organizations across all product and service sectors. What was considered a back office function is now credited as a key driver in producing great creative work. In 2016, we recognized that to keep up with the exponential growth in demand for content, the evolving group of Creative Ops Pros wanted a day dedicated to the subject. Since our first event in New York, it has grown rapidly in size, complexity and maturity and can now be…

Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 and Annex 11. However, unless one knows how to implement CSV, it is often very hard to detect the requirement for CSV, and very hard to determine what needs to be done, to meet domestic and /…

Overview: This lesson 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 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. I will speak on specific experiences from over 17 years of experience in working as an outsourced compliance auditor, expert witness on multiple HIPAA cases, and thoroughly explain…

Course "Risk Management in Medical Devices Industry" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Gaps, incorrect or incomplete implementation of software can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the development lifecycle. Diligent, complete and correct implementation of risk management from the start of product development is therefore imperative. This course will introduce all necessary steps to design, implement and test critical medical device software in a regulatory compliant environment. Software risk…

Overview: Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. Areas Covered in the Session: GMP Regulations that Apply to Analytical Laboratories Reviewing Documentation Advance Preparation for the Audit Auditing Styles and Structures Who Will Benefit: External and Internal Auditors Supervisors and Analysts in Quality Control Laboratories and Quality Assurance Groups Supervisors and Analysts in Contract Testing Laboratories Speaker Profile: Steven S. Kuwahara , Ph.D. is the founder…

Join us on our QS World MBA Tour in Washington DC this May 3rd, for an inspiring afternoon and evening of face-to-face networking opportunities, advice and exclusive offers. Whether you're simply looking for more information on how to get ahead in your career or on your way to applying for business schools, the event is packed full of resources to help you on your professional journey. Participating Business Schools Include: Univ. of Maryland, Robert H Smith, American University - Kogod, Fordham - Gabelli, Virginia Tech - Pamplin. Baruch College - Zicklin, University of Oxford - Said, Univ. of Sydney, Copenhagen…

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Training Options Duration: 60 Minutes Thursday, May 3, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: This webinar for HIPAA Covered Entities and Business Associates will identify the top OCR HIPAA enforcement priorities for 2018 and explain simply how you can master HIPAA compliance requirements for each enforcement priority. Why should you Attend: HIPAA Compliance is in crisis throughout the United States. The Office for Civil Rights (OCR), the HIPAA enforcement arm of the U. S. Department of Health and Human Services has just announced results of its recent HIPAA Compliance Audits of Covered Entities (CEs). The audited…

Supplier selection and management is a fundamental issue faced by medical device manufacturers. Suppliers are critical to the performance and safety of your device as well to your business. Neither the FDA nor your notified body regulates suppliers (with a few exceptions). Instead, they expect you have an effective process that ensures your suppliers perform. The regulators hold you responsible and verify your controls through inspections and audits. Consequently, you need to understand and implement the regulatory requirements for supplier management. You should pass an audit or inspection without any issues. This course delivers the tools, templates, and methods to…

This webinar will provide attendees with the knowledge and skills needed to develop and produce an OTC drug product for marketing and sale in the U.S. Learning Objectives: Gain a comprehensive understanding of how OTC drug products are regulated in the U.S. Learn to distinguish between a potential Rx pharmaceutical product and an OTC drug. Recognize the difference between the various pathways for commercializing an OTC drug product. Understand how to identify and successfully navigate an OTC Drug Monograph. Recognize when reliance on a Proposed Rule, Final Rule and/or Drug Monograph is appropriate. Understand how to determine whether an Ingredient…

OVERVIEW The basic provisions of privacy for protected health information are well known in HIPAA. Exceptions abound for various law enforcement purposes as applied to both the federal and state government and its law enforcement activities, including criminal and civil matters. Erase the uncertainty and doubt that exists when the health care practitioner is confronted with a police demand for information. What can you release? To whom? Do you have to notify the patient? Should you notify the patient? What must you document as a permitted disclosure when the police call? Find out in this informative webinar that arms you…

OVERVIEW This webinar will provide all the necessary tools to know how to properly process federal and state unemployment taxation and how you can reduce cost for unemployment taxation for your employer. In a time when employers are always looking for ways to reduce cost this webinar will give you tips to reduce taxation burdens. WHY SHOULD YOU ATTEND For years the only changes payroll professionals had to worry about was normal rate changes for state unemployment each year. But in recent years the IRS has made updates to the federal Form 940 and states are in a much different…

OVERVIEW Phase 2 of the new CMS requirements were to be in place by Nov. 28, 2017. We will look at most Phase 2 requirements in detail. Let this be a moment for your team to solidly know what is required and together assess your home’s compliance. Proven culture change practices that are now part of the Phase 2 requirements and those that contribute to compliance will be highlighted. WHY SHOULD YOU ATTEND This investment in time and thinking will assist you to solidly know what regulations pertain to your work. You will not be dependent upon others to tell…

OVERVIEW This will cover the history of Computer Systems Validation in the Pharmaceutical and Medical Device industries. This led to the regulation 21 CFR Part 11, which covers the management of both electronic signatures and electronic records. Compliance to relevant regulations using Standard Operating Procedures and required documentation will be covered. The roles of Audits, Quality Assurance, and Risk Management will also be covered. WHY SHOULD YOU ATTEND Changes continue to be implemented in many existing computer systems and in many cases computer systems are being replaced or upgraded using new technologies. Many of these changes require Validation and Validation…

Curso Exclusivo para canales de Palo Alto Networks : ¿Cómo vender la plataforma de Seguridad de Palo Alto Networks al sector financiero? ¡No se pierda de esta oportunidad exclusiva paa capacitarse con los expertos de Palo Alto Networks dentro del sector financiero! En este taller, diseñado específicamente para explorar los retos que enfrenta el sector financiero en materia de seguridad cibernética, usted podrá aprender las bondades de ofrecer a sus usuarios finales una verdadera plataforma de seguridad de nueva generación, automatizada y verdaderamente enfocada en la prevención. En este curso estudiaremos: - Posicionamiento del mensaje: diferenciadores clave en materia de…