Upcoming Medical Conferences in East BrunswickSearch Criteria : United States of America East Brunswick
Jun 13 - 14, 2019 | USD $720 | East Brunswick, New Jersey
It is great pleasure to welcome you to the American Conference on Advanced Treatments in Rare Diseases (RARE2019-USA), taking place on June 13-14, 2019 in East Brunswick, New Jersey, USA. Target Audience: RARE2019-USA is pleased to welcome professionals including: • Scientists • Clinicians • Pharmacists • Pathologists • Infectious Diseases Specialists • Health Care Professionals • Other Medical Professionals • Students • Clinical Research Organisations • Rare Diseases Associations • Research Networks • Pharmaceutical Companies • Orphan Drugs Companies Conference Topics: • Challenges in Rare Diseases • Lysosomal Storage Disorders as a Model - Biochemistry and Genetics • Lysosomal Storage Disorders as a Model - Specific Diseases and Therapeutic Options • New Therapies • Rare Diseases in Hematology • Rare Diseases in Nephrology • Rare Diseases in Neurology • Rare Disease - Generic Topics Conference Description: RARE2019-USA will follow on from the success of its European predecessor, addressing the challenges of Rare Diseases, their diagnosis and treatment as well as on new therapeutic modalities already in advanced stages of development. The Conference will expand on so-called "generic topics", such as clinical trials' design, funding for research, digital health, big data on the one hand and focusing on the individual patients for innovation in both drug development and management. RARE2019-USA are very fortunate to have a faculty that consists of world renowned speakers, all of whom are experts in the field of Rare Diseases and who will present ground-breaking and cutting-edge news on treatments in Rare Diseases, as you can see in the program. The Conference will provide participants an excellent opportunity to interact with all faculty members, consult, exchange views and to build up new collaborations and networking. RARE2019-USA is excited to welcome scientists and clinicians, pharmaceutical, clinical research organisations, research networks and other medical professionals. Join the Conference and benefit from expanding your network. Meet new friends, greet old colleagues and discuss new insights gained. RARE2019-USA looks forward to welcoming you to New Jersey.
Jun 13 - 14, 2019 | USD $1300 | East Brunswick, New Jersey
The American Conference on the New European Regulations of Medical Devices (RMD2019-USA) is organized by Bioevents and will be held from Jun 13 - 14, 2019 at Hilton East Brunswick Hotel & Executive Meeting Center, East Brunswick, New Jersey, United States of America. Target Audience: • Medical Device Companies • R&D personnel • QA Personnel • CEOs • Regulatory Affairs Specialists • CROs / CRAs • Research facility managers • Pharmaceutical Company representatives • Start-Up Companies Description: RMD2019-USA will follow on from the success of its European predecessors, (Prague 2016, Berlin 2017, Brussels 2018). In conjunction with EAAR (European Association of Authorized Representatives), our excellent panel of experienced professionals in this field will once again ensure a conference of noteworthy quality. Topics to be covered, among others will be: • Implementation of the New Regulations • The Road to 2020: Overview of Regulatory Developments • Major Regulatory Compliance Challenges for the Industry • Challenges for National Competent Authorities • New Legal Challenges to the Medical Device Industry • Scope, Borderlines and Classification • General Safety and Performance Requirements • Practical Aspects of Clinical Evaluation: What needs to be updated now and how to plan for ○ Future Compliance under the MDR • Impact of the MD/IVD-Regulations on Quality Management Systems • View of a Notified Body on the MDR Implementation Steps • Post-Market Surveillance • Do you need to plan for PMCF and What are the Possibilities for Gathering PMCF Data? • The Impact of Increased Transparency and Traceability Resulting from Eudamed and the ○ Introduction of UDI • Vigilance • What can we Expect from the MDR Authorized Representative? • Special IVD Issues • Software • Conflicts Between Economic Operators Additional details will be posted as soon as they are available.