Publication: All accepted papers of ICMMM 2017 will be published in the proceedings, which will be indexed by Ei Compendex, Inspec, DOAJ, CPCI Web of Science and Scopus. International Advisory Committees: Prof. Michael Pecht, University of Maryland, USA; Conference Chair: Assoc. Prof. Guanghsu Chang from Georgia Southern University, USA; Conference Program Chairs: Prof. Sergei Alexandrov, Institute for Problems in Mechanics, Russian Federation; Prof. Young Moon, Syracuse University, United States; Prof. QingZhi Zhai, China Agricultural University, China;

On behalf of the Conference series LLC it is our great pleasure to cordially invite you to participate to PSORIASIS 2017 2nd International Conference on Psoriasis, Psoriatic Arthritis & Skin Infections to be held on Oct 1617, 2017, New York, USA.

IEEE ATC 2017 will include a highly selective program of technical papers, accompanied by workshops, panel discussions, and keynote speeches. It will offer a forum for researchers to exchange ideas and experiences related to Advanced and Trusted Computing.

Theme for this years conference is "Building Healing Communities in Christ". Details to be announced in early spring of 2017.

Health, Wellness & Society Kledge Community: a conference and journal founded in 2011, exploring the intersections of human physiology and the conditions of social le.

PULSUS brings in a new spin on conferences by presenting the latest scientific improvements in Biomarkers and its clinical researches. Listen to motivating keynotes from thought leaders, pioneers across the globe. Atlanta is all set for an amazing event as PULSUS proudly presents the “Annual World Congress on Biomarkers & Clinical Research” on November 2728, 2017. PULSUS cordially welcome researchers, academicians, students and business professionals in the field of BIOMARKERS from around the world to participate in the upcoming BIOMARKERS CONGRESS 2017. The meeting for this year will revolve around the theme “Explore the latest Biomarkers development in health and clinical research” thus relaying the most cutting edge findings in the field of Biomarkers Research.

Dear SirMadam, I am writing to you from the Comprehensive NuclearTestBan Treaty Organization to share information about an upcoming conference which you, your students and your colleagues might be interested in. The CTBT: Science and Technology 2017 Conference SnT 2017 will take place from 26 to 30 June 2017 at the Hofburg Palace in Vienna, Austria. It will be the sixth in a series of multidisciplinary conferences designed to further enhance the strong relationship between the scientific and technological community and the CTBTO. The conference series provides a forum for scientists from around the world to exchange knowledge and share advances in monitoring and verification technologies of relevance to the Comprehensive NuclearTestBan Treaty CTBT. Such interaction helps ensure that the Treaty’s global verification regime remains at the forefront of scientific and technical innovation. The 1996 Comprehensive NuclearTestBan Treaty CTBT bans all nuclear explosions by everyone, everywhere: on the Earths surface, in the atmosphere, underwater and underground. The CTBTO is tasked with establishing a verification regime which includes a global network of over 300 monitoring stations. I would be grateful if you could share information about the Conference and encourage students and colleagues to submit abstracts and attend. Please find attached a short electronic flyer. We would also be happy to provide you with printed posters and flyers for distribution. For more information, including on financial assistance, submission deadlines and the themes of the Conference, please see https:www.ctbto.orgspecialssnt2017 Please do not hesitate to contact us with any questions that are not covered on the website. We look forward to hearing from you and to hopefully welcoming you in Vienna next June. Sincerely, SnT2017 Local Organizing Committee SnT@ctbto.org THEMES: The Earth as a Complex System Events and Nuclear Test Sites Advances in Sensors, Network and Processing Performance Optimization and System Engineering Monitoring for Nuclear Explosion in a Global Context GOALS: To enlarge the scientific community engaged in testban monitoring, including among young scientists To promote the wider scientific application of data that is used for testban verification To enhance the exchange of knowledge and ideas between the CTBTO and the broader scientific community The present to the scientific community the needs of nuclear test monitoring and verification CALL for PAPERS, DEADLINE for ABSTRACT SUBMISSION: 6 FEBRUARY 2017

We request abstracts on variety of themes of South Asian society and State relationship, dferent religions and emergence of cultssect in these religions; rise of guilds, economies, development of branches of kledge, historical transition from ancient to modern times and many more.

“International Conference on Pharmaceutical and Biomedical Engineering” Pharma Engineering 2017 scheduled to be held during October 1617, 2017 at Osaka, Japan. Theme: Recent Innovations in Pharmaceutical and Biomedical Engineering

On "Advances and Trends in Engineering Materials and their Applications".

The Congress will provide the opportunity for a comprehensive overview of the latest research developments in cardiovascular medicine, primarily in the areas of Molecular and Cellular Cardiology, Genetics of Heart Disease, Cardiac Imaging, Coronary Artery Disease, Peripheral Arterial Disease, Interventional Cardiology, Lipoprotein Disorders, Hypertension, Diabetes Mellitus, Heart Failure, Valvular Heart Disease, Diseases of the Aorta, Cardiac Arrhythmias and Electrophysiology, Antiarrhythmic Devices, Sudden Cardiac Death, Pediatric Cardiology, Congenital Heart Disease, Cardiac Surgery, Heart Transplantation, Mechanical Circulatory Support and Measurement of Outcome and Quality of Cardiovascular Care. Plans for this CME meeting are progressing extremely well, and as of now over 150 of the most distinguished cardiologists and scientists have agreed to join the faculty participating in this Congress. Papers will be presented in the form of plenary sessions, symposia and posters, and will include superb scientific material originating from numerous laboratories around the globe.

The International Conference of Theoretical and Applied Nanoscience and Nanotechnology TANN17 aims to become the leading annual conference in fields related to nanoscience and nanotechnology. The goal of TANN17 is to gather scholars from all over the world to present advances in the fields of nanoscience and nanotechnology and to foster an environment conducive to exchanging ideas and information. This conference will also provide an ideal environment to develop new collaborations and meet experts on the fundamentals, applications, and products of the mentioned fields.

On "Advances and Trends in Engineering Materials and their Applications".

Conference series LLC invites all the participants across the globe to attend the "3rd World Gynecologic Oncology Congress” CME Accredited and slated on July 2021, 2017 Chicago, USA Global Gynecology Oncology conferences provides two day of robust discussions on methods and strategies related to management and quality improvement of Cancer therapy as well as explore new ideas and concepts on a global scale and topics include ovarian cancer, Breast cancer, uterine cancer, vaginal cancer, cervical cancer, and vulvar cancer.

9th International Conference on Bioinformatics Paris, France Dates: October 2324, 2017 Venue: Paris, France On behalf of the Organizing Committee Members, we would like to invite everyone interested in the field of Bioinformatics to the 9th International Conference on Bioinformatics which will explore the latest research on Bioinformatics through diverse scientific topics. The event is scheduled during October 2324, 2017 at Paris, France. The conference revolves around the theme Exploring the latest innovations in Bioinformatics. The conference will gather grand expertise at the global platform to feature the most innovations to fulfill the needs of bioinformatics resources & technologies for the future research. Conference Website: http:bioinformatics.conferenceseries.com Conference Highlights: • Bioinformatics And Computational Biology • Systems Biology In Bioinformatics • Emerging Trends In Proteomics • Emerging Trends In Genomics • Health Informatics In Bioinformatics • Structural Bioinformatics • Evolutionary Bioinformatics • Biostatistics An Approach To Bioinformatics • Bioinformatics Algorithms & Databases • Bioinformatics Tools And Software • Immunology And Drug Discovery • Perspectives Of Clinical Informatics • Epigenetics • Clinical Case Reports For abstract submission, please find the link: http:bioinformatics.conferenceseries.comabstractsubmission.php For more queries, mail us at: bioinformaticscongress@biochemconferences.org

Join us at our 2017 International Conference on Education Stockholm, at the Scandic Continental – Stockholm! The conference provides a forum for faculty and administrators to share proven and innovative methods in teaching at all levels of education. In addition to the Education Conference, we are also hosting an Academic Conference on Business and the Conference on Technology in Education that will be held on the same days, at the same venue. One registration fee will allow you to attend all three conferences. All conference submissions are peer reviewed inhouse with a blind peer review available upon request. We also publish doubleblind, peer reviewed academic journals with impact factors.

The International Conference on the Science and Engineering of Materials ICoSEM is back…! This biennial conference aims to provide a platform for scientists, researchers, engineers, and students within the region to exchange knowledge on the recent development and progress in the field of Materials Science and Engineering. The previous ICoSEM conferences in 2013 and 2015 were highly successful and attracted an increasing number of participants from academia and industry. This year, the 3rd International Conference on the Science and Engineering of Materials 2017 will be held on 2425 October 2017 in Kuala Lumpur, Malaysia.

Course "Good Clinical Practices GCP Understanding and Implementing the Current Global Requirements" has been preapproved by RAPS as eligible for up to 12 credits towards a participants RAC recertification upon full completion. Overview: • Defining the basic requirements of Good Clinical Practices • Clinical Study Protocol Elements and Device Accountability • Role of Institutional Review Board IRB and Informed Consent • Principles of Ethics and Quality Control • Determining the appropriate duties and oversight required of the sponsor, monitor, and investigators to ensure a high level of quality in a clinical trial • Ensuring that quality practices are designed and implemented to guarantee compliant clinical trials • Learning how to effectively manage a Sponsor, as well as, an FDA GCP inspection • Developing mechanisms to uncover and preclude fraud and misconduct in clinical trials • And Much More... Why should you attend: • What is GCP and why is it needed? • History and development of GCP in EU and US and where are we now? • Managing problem areas of working with GCP regulations and guidelines • Impact of GCP globally and key FDA differences • Recognize the regulatory pathways in the U.S • Explore practical aspects of investigator and monitor selection • Discuss how to comply with the fundamentals of Good Clinical Practice GCP • Examine practical aspects of conducting international clinical trials • Understand the significance of Ethics and Human Subject Protection • Understand how to prepare for audit and inspection of clinical trials • Recognize what prompts an FDA audit • Learn how to plan for an audit or inspection, including using appropriate checklists • Appreciate how to prepare for auditinspection Interviews • Consider how to respond to the auditinspection findings • How to monitor clinical trials effectively and efficiently • Comprehensive overview of the applicable regulations on good clinical practice and clinical trials • Attendees are encouraged to discuss GCP work related activities associated with their functional area on the various topics as applicable for interactive group discussion • Review and discuss pain points, challenges and solutions Areas Covered in the Session: • Adherence to ethical principles as laid out by the Helsinki Declaration • Good Clinical Practice regulations require that clinical trials be consistent with regulatory requirements • Good Clinical Practice regulations require the sponsor to make available clinical and nonclinical data from the study to support further related research • Trials should thoroughly assess the risks and benefits inherent in a clinical research • The clinical research should ensure the wellbeing of its subjects • Good Clinical Practice regulations require sponsors of a clinical trial to contain a clearly defined protocol that should be rooted in established scientific principles and practices • A clinical research program must be subject to oversight from an independent Ethics Committee • Good Clinical Practice regulations requires the sponsor to obtain informed consent from each of the subjects • Good Clinical Practice regulations requires adherence to set documentation practices • There should be thorough confidentiality of information relating to the subject • The adherence to applicable Good Manufacturing Practices GMP by the sponsors when it comes to the manufacture, storing and handling of investigational products is another requirement of Good Clinical Practice regulations • The principles of Good Clinical Practice regulations require the implementation of systems with procedures that bring about complete quality at every stage of the clinical trial • New Clinical Trials Regulation EU No. 5362014 repealing Directive 200120EC • GCP Regulations, Guidance and Additional Resources Who Will Benefit: This seminar will provide an overview and indepth snapshot of GCP regulations with a global overview. Employees who will benefit include all levels of management and departmental representatives from key functional areas and those who desire a better understanding or a "refresh" overview of the GCP process, including • Clinical Research Associates who want a greater understanding of the medical device clinical trial process and their role in it • Clinical Project Managers who are taking on a wider range of responsibilities and need to gain a greater understanding of the regulatory and practical issues involved in medical device clinical trials • Regulatory Affairs Professionals who may be new to the device industry or new to the clinical trials process • Clinical Investigators and Clinical Research Coordinators interested in gaining a broader understanding of their role and responsibilities and how these tasks relate to the overall research process • Regulatory Affairs Management • Regulatory Affairs Specialist • Auditors • Compliance Specialist • Clinical Affairs • Quality Assurance Management • Consultants Agenda: Day 1 Schedule Good Clinical Practices • Introductions and Background • What is GCP? • Why should we have GCP? ICH GCPFDA CFR GCP • The Basic Principles of FDA and ICH GCP • The 13 Basic Principles of ICH GCP • Key ICH Guidelines and FDA Resources • Compliance Guidance Manuals • Impact of ICH GCP in the US • FDA Acceptance of Foreign Studies • FDA GCP Regulation • FDA and International Regulations and Guidance Relating to Good Clinical Practice and Clinical Trials • FDA and Institutional Review Board IRBIndependent Ethics Committee IRBIEC • Responsibility of the IRBIEC • Subject Informed Consent Forms • Informed Consent of Trial Subjects • IRBIEC interactions with Sponsors and Investigators • FDAs IRB requirements • FDA Responsibilities of Sponsors and Investigators • Investigator Records and Reports and Other Required Documentation for Good Clinical Practices • Disqualification of a Clinical Investigators • ICH Sponsor Responsibilities • FDASpecific Sponsor Responsibilities • Working with Contract Research Organizations CROs • Trial Management • Data Management • Recordkeeping and Documentation • Compensation to Subjects and Investigators and Other Financial Considerations Exercise and Recap of Day 1 • Clinical and Data Management Discussions • Review of Regulatory Documents Day 2 Schedule Good Clinical Practices • Monitor Responsibilities • Complying with the Protocol, Amendments, SOP and Guidance • Fraud and Misconduct • Safety & Adverse Event Reporting • Clinical Trial Protocol and Amendments • Investigator Brochure Requirements • Essential Documents • Tips for Regulatory Inspections Common Findings • Bioresearch Monitoring Program BIMO • BIMO inspection metrics clinical investigators, IRBs, sponsors, etc. • Reporting Complaints Related to FDARegulated Clinical Trials • GCP Inspections • Additional FDA Guidelines and Resources Exercise and Recap of Day 2 • Clinical and Data Management Discussions • Review of Regulatory Documents DebriefAdjourn • Recap of topics and key discussion points and take away message • FAQs and latest trends Speaker David R. Dills Global Regulatory Affairs & Compliance Consultant David R. Dills, Global Regulatory Affairs & Compliance Consultant currently provides regulatory affairs and compliance consultative services for earlystage and established Class IIIIII device, IVD, biopharmaceutical, cosmetics and nutraceutical manufacturers on the global landscape, and has an accomplished record with more than 27 years of experience in the areas of Regulatory Affairs, Compliance and Quality Systems. He has been previously employed, with increasing responsibilities by device manufacturers and consultancies, including a globally recognized CRO and has worked directly with manufacturers engaged in compliance remediation activities involving consent decrees, CIAs, warning letters, and customer generated compliance events, conducts QS, regulatory, compliance assessmentsaudits and FDA Mock Inspections for State of Readiness. He has been directly involved with constructing, reviewing, and remediating regulatory submissions, U.S. Agent for OUS companies, works closely with the key stakeholders and AgencyCenter Reviewers regarding submission meetings and negotiations; clinical affairsCTM and provides regulatory submissions and postmarket project leadership and guidance covering multiple therapeutic and medical specialties based on classification. He has a strong background in the interpretation and applicability of FDA and international regulations, leads activities for the registration and approval process and working with the Agencies in Asia Pacific, EMEA and The Americas, including FDA, European Medicines AgencyEMA, MHRH, ANVISA, PMDA, MOH, CFDA, TGA, and Health Canada and works with management on regulatory strategies and plans supporting a companys commercialization strategy. He directs and leads efforts for PM support involving all phases of the premarketing to postmarketing; establishes Medical Device Single Audit MDSAP, UDI, and Digital MarketingPromotionAdvertising compliance strategies; lead efforts regarding AEIncident Reporting, all aspects of Postmarketing Surveillance and Vigilance Reporting; establish QMS and documentation systems for GxP compliance; ISO 13485 registration and CE Mark, Technical File, Design Dossier and CER consultation; and facilitates multicountry product registrations and licensing. He recommends action to senior leadership to ensure effective resolution for manufacturers to achieve sustainable and proven compliant systems. Background encompasses broad capabilities in quality systems; documentation development and remediation; regulatory oversight and governance; design controls; CAPA investigations; GxP training; software embedded medical devicesall aspects of SWSDLC and process validation with compliance oversight; supplier management; and demonstrates credible experience to optimize business performance through proactive strategies to mitigate compliance exposure. Mr. Dills has served on the Faculty Advisory Board for the Pharmaceutical Training Institute, Editorial Advisory Boards for Software Quality Professional and the Institute of Validation Technology IVT, publisher of the Journal of GXP Compliance and Journal of Validation Technology and on the Readers Board for Medical Device & Diagnostic Industry and Medical Product Manufacturing News and was nominated and accepted for inclusion into the 20052006 Strathmores Whos Who of Professionals. Mr. Dills has authored and published validation, regulatory and compliancerelated articles, commentaries and technical guides, and is an accomplished global industry presenter. Mr. Dills academic degrees include Environmental Science and Biology. He is a former Chair and Co Chair of ASQs Section 1506 and affiliated with the Biomedical Division, RAPS, AdvaMed, PDA, ISPE, and other industry working groups. Location: Zurich, Switzerland Date: June 15th & 16th, 2017 and Time: 9:00 AM to 6:00 PM Venue: Hilton Zurich Airport Address: Hilton Zurich Airport Hohenbuhlstrasse 10, 8152 OpfikonGlattbrugg, Switzerland. 41 44 828 50 50 Price: Register now and save $200. Early Bird Price: $1,695.00 Seminar Fee for One Delegate Until May 10, Early Bird Price: $1,695.00 From May 11 to June 10, Regular Price: $1,895.00 Register for 5 attendees Price: $5,085.00 $8,475.00 You Save: $3,390.00 40% Quick Contact: NetZealous DBA as GlobalCompliancePanel Phone: 18004479407 Fax: 3022886884 Email: john.robinson@globalcompliancepanel.com Website: http:www.globalcompliancepanel.com Registration Link – http:www.globalcompliancepanel.comcontrolglobalseminars~product_id900976SEMINAR?worldconferencealerts_SEO Follow us on LinkedIn: https:www.linkedin.comcompanyglobalcompliancepanel Like us our Facebook page: https:www.facebook.comTrainingsAtGlobalCompliancePanel Follow us on Twitter: https:twitter.comGCPanel

Overview: Richard Mills delivers indepth insights on incentivizing individuals, teams and entire organizations with plans that reward positive results and acknowledges mutual success. Territorial concerns and isolationist actions can be avoided with the proper balance of targets, metrics and milestones. When goals are set for a single sector of the organization and they do not match the goals of another sector, then offsets must be applied to compensate for the actual control that each group has to achieve their respective goals.

The conference will cover vital issues in medical, medicine and health sciences under multiple subthemes. The aim of our conference is to support, encourage and provide a platform for networking, sharing, publishing and nurturing the potential growth of individual scholars across the globe. Selected conference papers will be published in associated Scopus ISI indexed journal. All other papers will be considered for Google scholar index journals.

The conference will cover vital issues in Engineering & Technology, Computer, Basic and Applied Sciences Research & Practice under multiple subthemes. The aim of our conference is to support, encourage and provide a platform for networking, sharing, publishing and nurturing the potential growth of individual scholars across the globe. Selected conference papers will be published in associated Scopus ISI indexed journal. All other papers will be considered for Google scholar index journals.

The conference will cover vital issues in Business, Economics, Social Sciences and Humanities under multiple subthemes. The aim of our conference is to support, encourage and provide a platform for networking, sharing, publishing and nurturing the potential growth of individual scholars across the globe. Selected conference papers will be published in associated Scopus ISI indexed journal. All other papers will be considered for Google scholar index journals.

The conference will cover vital issues in medical, medicine and health sciences under multiple subthemes. The aim of our conference is to support, encourage and provide a platform for networking, sharing, publishing and nurturing the potential growth of individual scholars across the globe. Selected conference papers will be published in associated Scopus ISI indexed journal. All other papers will be considered for Google scholar index journals.

The conference will cover vital issues in Business, Economics, Social Sciences and Humanities under multiple subthemes. The aim of our conference is to support, encourage and provide a platform for networking, sharing, publishing and nurturing the potential growth of individual scholars across the globe. Selected conference papers will be published in associated Scopus ISI indexed journal. All other papers will be considered for Google scholar index journals.