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Dallas Makerspace Meetup
4/24/2014 7:00 PM - 9:00 PM
Dallas Makerspace Dallas, Texas United States
Event Listing

Thursday nights are weekly activity and coordination meetings for Dallas Makerspace! Come visit if you'd like to participate, and be sure to bring any special project that you would like to show off to the rest of the group.

Data Center Design Webinar By EITAGlobal
4/30/2014 10:00 AM - 11:30 AM
Online Event(World wide) Fremont, California United States
Event Listing

Areas Covered in the Session:

Is a data center the right option




Infrastructure design

Energy efficiency


Who Will Benefit:




Data center Managers

Data center Designers

Data center Operators

Demo Day
4/25/2014 4:30 PM - 6:00 PM
Davis Roots Davis, California United States
Event Listing

Join us for our inaugural Demo Day! Our second class of companies (EveryLevel, The Gift of Education and Fishrock Labs) will be presenting, demoing their products and giving their pitches. Our incoming third class of companies will also be present and will be giving short presentations on their technology and products. There will be a Q&A with the individual companies at the end of their presentations.

Denton Jelly
4/25/2014 10:00 AM - 5:00 PM
Banter Coffee House Denton, Texas United States
Event Listing

Chances are, if you can work from a laptop, you will fit in here. The most common traits shared by Jelly attendees are the entrepreneurial spirit, and a love for technology. We also hope to see a good turnout of tech-lovin' college students.

Effective Portfolio Management Webinar By EITAGlobal
5/13/2014 10:00 AM - 11:30 AM
Online Event(World wide) Fremont, California United States
Event Listing

This webinar is about Effective Portfolio Management. The objective is to help insure that you prioritize and select the right project for your strategic objective so you can manage this portfolio with agility and flexibility in order to adapt to "real life" while delivering the results as required. Are you funding the right projects? Is your staff working on the right task? Are you getting maximum value with the investments you have? Effective Portfolio Management is about getting the highest value of your investments while delivering the best value in accordance with the vision, principles and organization priorities.

Entrepreneurship Sessions with Sameer Shalaby
4/28/2014 2:00 PM - 4:00 PM
ThinkLab at the University of Mary Washington Fredericksburg, Virginia United States
Event Listing

The iCenter is a startup incubator that was founded, by Sameer Shalaby, in October 2013 to help entrepreneurs, and members of the Fredericksburg community formulate their business ideas to incubate and take them from a successful launch successful to funding to ultimate exits.

Eseed Entrepreneurship Training
2/24/2014 1:00 AM - 5/19/2014 4:00 AM
FVTC Waupaca Regional Center Waupaca, Wisconsin United States
Event Listing

E-seed™ assists start-up, early-stage entrepreneurs and experienced small business owners in developing management and planning tools for their businesses.

Eseed Entrepreneurship Training
5/13/2014 6:00 PM - 8/12/2014 9:00 PM
D.J. Bordini Center Appleton, Wisconsin United States
Event Listing

Thinking of starting a business? Need help? E-seed™ assists start-up, early-stage entrepreneurs and experienced small business owners in developing management and planning tools for their businesses.

Ethical Issues in Human Subjects Research Webinar By MentorHealth
5/7/2014 10:00 AM - 11:00 AM
online event Fremont, California United States
Event Listing

Overview: This webinar is a compilation of information in areas that generate the most questions for human subject's researchers when conducting research internationally. Discussed in this webinar will be: 45 CFR 46.111 (a)(2) which states, "In evaluating risks and benefits, the IRB should consider only those risks and benefits that may result from the research (as distinguished from risks and benefits of therapies subjects would receive even if not participating in the research)." So what is risk assessment and how does that affect you? The Criteria for Approval found in both the FDA and HHS regulations stipulates what will be looked at during the approval process yet many do not know how, under which conditions, their study is reviewed and therefore do not anticipate possible questions in their study design.

The Federalwide Assurance is required for NIH funded studies. It is a written assurance filed with the Office for Human Research Protections (OHRP) that outlines under which terms a study will be reviewed, approved, and conducted. Even if the study is not NIH funded the principles in the Federalwide Assurance apply. Because of this assurance, additional criteria get applied to studies. When does that happen? Why? Can it be avoided? These questions and more will be answered by learning the information presented in this webinar.

Why should you attend: All researchers want their studies be reviewed and approved quickly. Most investigators do not think about regulatory criteria when designing a study. Complicating matters is the current trend to conduct research in private physician offices and other community venues. Although this makes research more accessible to potential participants, it also invokes another set of regulations and requirements.

The consent document and process are always areas that generate questions. What can and cannot be used? Why? What is allowable? Risks, benefits and how those are viewed and accessed also confound and befuddle individuals working in this field. Knowing what to consider and what the possible stumbling blocks could be, make getting an approval to conduct human subject's research easier. Attendance at this webinar will do just that. It will not only give you a working knowledge of the areas that create the most confusion, it will also give you an understanding that will help you avoid or work through these areas faster and be of assistance to those around you.

Areas Covered in the Session:

Assurances: What are these? What do they stipulate? How they affect you as a researcher

Criteria for review. What to think about and consider when developing or conducting your study

Consent and assent. What is required? What choices do you have?

Community research. What is involved when you ask a private physician to conduct your study or to recruit from his/her clinic?

Risk/Benefit Assessment. What is it? Who makes the determination? What does that determination mean with regards to additional requirements? What is allowable?

Who Will Benefit:

Principal Investigators / Sub-investigators

Clinical Research Scientists (PKs, Biostatisticians,)

Safety Nurses

Clinical Research Associates (CRAs) and Coordinators (CRCs)

Recruiting Staff

QA / QC auditors and Staff

Clinical Research Data Managers

Human Research Protection Professionals

Sarah Fowler-Dixon, PhD, CIP is Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for human subject research which has served as a model for other institutions. She crafted budgets, policies, procedures, reporting, and training for the new program. She has initiated the planning, development, authorship and implementation of many human subjects research policies, practices, guidelines, submission and reviewer forms often working with state and federal authorities.


Phone No: 800-385-1607

FaX: 302-288-6884

Event Link:

Eugene Startup Weekend
5/2/2014 6:00 PM - 5/4/2014 9:00 PM
University of Oregon's Erb Memorial Union, EMU Eugene,, Oregon United States
Event Listing

Startup Weekends are 54-hour events designed to provide superior experiential education for technical and non-technical entrepreneurs. Beginning with Friday night pitches and continuing through brainstorming, business plan development, and basic prototype creation, Startup Weekends culminate in Sunday night demos and presentations.

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