All Conferences

International Conference on 2018 ISMAC - CVB in Computational Vision and Bio-Engineering (2018 ISMAC - CVB) is being organized on 16-17 May 2018 by SCAD Institute of Technology at Coimbatore, India. I-SMAC will provide an outstanding international forum for sharing knowledge and results in all future fields of Internet of Things, Social, Mobile, Analytics and Cloud. I-SMAC provides quality key experts who provide an opportunity in bringing up innovative ideas. Recent updates in the in the field of Computational Vision and Bio-Engineering will be a platform for the upcoming researchers. The conference will be Complete, Concise, Clear and Cohesive in…

13th International Conference on Advances in Biology, Nursing, Pharmaceutical and Medical Sciences (ABNPMS-18) scheduled on March 19-20, 2018 at Dubai (UAE) is for the researchers, scientists, scholars, engineers and parctitioners from all around the world to present and share ongoing research activities. All accepted papers of ABNPMS-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 DiRPUB's Digital Library. The Proceeding will be also submitted to SCOPUS/ISI Thomson for review. In addition the proceedings will…

The theme invites ideas on how to achieve more efficient use of resources based largely on the IoT-based machine-to-machine (M2M) interactions of millions of smart meters and sensors in the smart grid specific communication networks such as home area networks, building area networks, and neighborhood area networks. The smart grid also encompasses IoT technologies, which monitor transmission lines, manage substations, integrate renewable energy generation (e.g., solar or wind), and utilize hybrid vehicle batteries. All accepted papers will be published by Springer and made available through SpringerLink Digital Library, one of the world’s largest scientific libraries. Proceedings from EAI conferences are…

In an age of uncertainty, the one certainty for 2018 is the introduction of the European General Data Protection Regulation (GDPR). In order to assist European organisations take a practical, business orientated approach to GDPR, the team at MetaCompliance are having an executive briefing in key European cities. These include London, Dublin, Edinburgh, Amsterdam, Berlin and Geneva. Whether you are kickstarting your privacy project or looking for ways to ramp up your existing programs, these breakfast briefings are designed to provide practical advice and assistance. Focusing on the realities of implementing GDPR, these practical briefings will expand on our team's…

Fur einen Tag werden Berlin und Munchen zu dem Ort fur Social Media Marketing. Auf vier Buhnen gleichzeitig, mit uber 40 Speakern und groBen Pausen furs Networking erlebt ihr die AllFacebook Marketing Conference. Ihr trefft Mitstreiter aus der Branche, tauscht euch aus und kommt mit neuen Ideen, Strategien und Konzepten nach Hause. Egal ob Einzelkampfer, kleines Unternehmen, Mittelstand oder Großkonzern – wir spielen alle mit den gleichen Netzwerken. In hochkratigen Sessions werden Inhalte vermittelt, die besonders fortgeschrittene Nutzer ansprechen, aber auch fur Anfanger einen guten Einstieg bieten. Am Workshoptag bekommt man als Teilnehmer bei intensiven Seminaren zusatzliche Einblicke ins Facebook…

It gives us great pleasure to invite you to the 20th European Congress of Endocrinology (ECE 2018), on behalf of the European Society of Endocrinology (ESE), the Programme Organising Committee and the Local Organising Committee. ECE is designed to support scientific and professional interaction among all fields of endocrinology and metabolism, from bench to bedside, with the aim of advancing knowledge and improving patient care. Continuing the excitement and momentum of ECE 2017 in Lisbon, Portugal, the Programme Organising Committee has created a scientific programme featuring the best international, European and local experts as speakers in a versatile scientific programme…

MobiMedia is intended to provide a unique international forum for researchers from industry and academia, working on multimedia coding, mobile communications and networking fields, to study new technologies, applications and standards. Original unpublished contributions are solicited that can improve the knowledge and practice in the integrated design of efficient technologies and the relevant provision of advanced mobile multimedia applications. MOBIMEDIA proceedings are indexed in leading indexing services, including EI Elsevier Engineering Index, Scopus, CrossRef, Google Scholar, DBLP, as well as EAI’s own EU Digital Library (EUDL). Best Paper Awards The Conference Chairs and Program Committee for the EAI’s MOBIMEDIA 2018…

In an age of uncertainty, the one certainty for 2018 is the introduction of the European General Data Protection Regulation (GDPR). In order to assist European organisations take a practical, business orientated approach to GDPR, the team at MetaCompliance are having an executive briefing in key European cities. These include London, Dublin, Edinburgh, Amsterdam, Berlin and Geneva. Whether you are kickstarting your privacy project or looking for ways to ramp up your existing programs, these breakfast briefings are designed to provide practical advice and assistance. Focusing on the realities of implementing GDPR, these practical briefings will expand on our team's…

12th International Conference on Chemical, Waste Management, Genetics, Cellular and Molecular Biology (CWGCMB-18) scheduled on March 19-20, 2018 Dubai (UAE) is for the researchers, scientists, scholars, engineers and parctitioners from all around the world to present and share ongoing research activities. All accepted papers of CWGCMB-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 DiRPUB's Digital Library. The Proceeding will be also submitted to SCOPUS/ISI Thomson for review. In addition the proceedings will be…

You'll talk to and hear from the best of the best - including major job boards, technology providers, start-ups and investors. We'll bring market leading players and interesting start-ups about each of each of the below mentioned topics on stage. We'll help you to make your business futureproof. At RecPlus experts will give their views and – most important – attendees and exhibitors will talk to each other extensively. RecPlus will provide excellent networking opportunities and through our event app attendees can book meetings with each other even before the event starts. The 2018 RecPlus program will focus on five…

Being the HIPAA Security and Privacy Official involves not only ensuring you know 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 breach investigation, 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 of a HIPAA compliance program. If your HIPAA Security and Privacy Official needs to understand what…

The FDA is increasing its enforcement actions both for domestic and foreign inspections. Enforcement statistics have not been summarized yet because 2017 has not ended yet. We are certainly seeing more Warning Letters and Import Alerts based on Data Integrity (21 CFR Part 11: Electronic Records; Electronic Signatures. In the past FDA used to issue several Warning Letters to the same firms upon consecutive inspections. Today, after receiving one Warning Letter the next regulatory action is elevated to Import Alert, Consent Decree, and Injunctions for domestic manufacturers. Senior Management must take the initiative in setting the tone of full compliance:…

Gaps, incorrect or incomplete implementation of safety functionality 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 devices in a regulatory compliant environment. This course will additionally address the software risk management and the resulting interfaces to device level risk management. To comprehensively summarize all risk related activities and to demonstrate the safe…

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…

Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials and services to the device manufacturer, which means that they can be critical to performance and delivery of your device. Neither the FDA nor your notified body regulates your suppliers (with a few exceptions). They expect you to have an effective process to ensure your suppliers perform in the regulatory environment. How well do you understand the requirements for supplier management? Could you pass a regulatory audit or inspection without any issues? This course delivers the tools, templates, and methods to help participants…

This interactive two-day course explores proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. Many companies are outsourcing IT resources and getting involved with Software as a Service (SaaS) and cloud computing. These vendors are not regulated and therefore regulated companies must ensure compliance for both infrastructure qualification and computer system validation. It is the regulated company that wants to avoid FDA form 483s and warning letters. The seminar is intended for regulated companies, software vendors, and SaaS/Cloud providers. The instructor addresses the latest computer system industry standards for data security, data transfer,…

Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials and services to the device manufacturer, which means that they can be critical to performance and delivery of your device. Neither the FDA nor your notified body regulates your suppliers (with a few exceptions). They expect you to have an effective process to ensure your suppliers perform in the regulatory environment. How well do you understand the requirements for supplier management? Could you pass a regulatory audit or inspection without any issues? This course delivers the tools, templates, and methods to help participants…

This two day seminar takes the participants through HIPAA compliance from start to compliance. The first presentation explains the history of HIPAA, why it came to being and its evolution. This covers what HIPAA is, what steps have to be performed to be HIPAA compliant and what HIPAA compliance is. It also provides definitions to key HIPAA terms, how to define a Business Associate and how to contract with Business Associates. The second part of the first presentation is an overview of how to manage the HIPAA compliance project. At the end of these presentations there will be a workshop…

This 2 day course will cover practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and activity planning. This two day interactive course will cover fundamental principles of a cleaning validation program, exploring such concepts as the determination of residues to be targeted, selection of analytical and sampling methods, determination of appropriate limits in various pharmaceutical and biotechnology processes, and establishment of scientific rationales acceptable to regulatory inspectors. The program will describe the requirements for establishing an effective cleaning validation program, including the development of a general policy, a "Cleaning Validation Master Plan"…

The medical device industry is in the midst of major change, with the publication of the FDA's UDI Regulation, the first revision to the ISO Quality Management Systems standard in over a decade, and the upcoming changes to the EU's Medical Device Regulation expected to be passed later this year. All of these events have far reaching effects on Quality Management Systems so it is critical to understand what has changed with in ISO 13485: 2016 in order to create a comprehensive quality plan for your organization to ensure continued compliance and certification. This interactive session will include lectures, roundtable…