The Defense Logistics Agency's annual spring golf tournament offers sponsorship opportunities. By being a sponsor, you can play golf alongside approximatley 130 employees of the Headquarters Complex (home to the HQ of DLA, DCAA, DTIC, and DTRA) on the beautiful Fort Belvoir course and promote your company! Registraon starts at 6:30 AM and golfers are able to enjoyearly morning pracce balls. The HQC Site Director, Mr. John Holwick, briefsthe go...

Are you nearing separation or retirement and looking for an IT, Technical or Intelligence Job? Do you have an active federal security clearance and interested in finding new career opportunities? Meet defense, technical and intelligence focused organizations face to face to build your network and explore job and professional development opportunities. Our technical, intelligence and security clearance focused hiring fair allows service members...

On 30th April & 1st May 2018, join 1000 leaders defining the future of the aerospace, aviation, defence and space industry. The Global Aerospace Summit is where corporate, government and military strategies are marked out. What do future aircraft need to look like? How will new processes and technologies revolutionize manufacturing? What threats does a distributed, digital world hold for incumbents’ business, and where are the game c...

You're invited for an evening of networking immediately following the closing remarks at ENGAGE311.Continue socializing with your colleagues over hors d'oeuvres and an open bar. American Social boasts a great view of the bay and is conveniently located in the same building as the West Tampa Waterside.Additionally, be sure you're scheduled to see Salesforce's elite sponsor presentation on Monday from 1:45-2:30pm. We'll be in Oasis Ballroom on f...

BUILDING THE CYBER TEAM – EDUCATION, RESEARCH, TRAINING AFCEA International is pleased to host the first Cyber Education, Research, and Training Symposium (CERTS) connecting military and agency stakeholders with solution providers from academia, business and research centers. CERTS will feature keynote speakers, panels and breakout sessions promoting discussion between operators and supporting professionals. It will include information...

Training Options Duration: 60 Minutes Monday, December 4, 2017 | 10:00 AM PDT | 01:00 PM EDT Overview: FDA 7348.811 section 1 states, "Regardless of the type of system used by the clinical site, the regulatory requirements for clinical data do not change whether clinical data are captured on paper, electronically, or using a hybrid system." What type of system is best for your program and investigator capabilities? The wrong choice yields insp...

WHERE: HILTON GARDEN INN & BANQUET CENTER, 3520 PENTAGON BLVD., BEAVERCREEK, OHIO PRE-LUNCHEON CHECK-IN/NETWORKING: 11:30AM-11:45AM LUNCHEON TIME: 11:45AM-1:00PM RSVP REQUIRED: BY 5PM ON FRIDAY, OCT.15, 2017 - ON OUR ONLINE SYSTEM **ONLINE PRE-REGISTRATION IS STRONGLY ENCOURAGED TO HELP THE AFCEA CHAPTER AND HGI FACILITATE AND ORGANIZE THE LUNCHEONS TO MEET THE NEEDS OF ALL GUESTS.** ONLINE REGISTRATION SYSTEM: INDIVIDUAL REGISTRATION: All...

Good Laboratory Practice (GLP) is a quality system which intend for non-clinical studies and was revised by several bodies. GLP is a unique quality system in the sense it is intend for non-routine processes and activities. Why should you Attend: The authorities often required a GLP declaration and statement for submitted studies. Come to hear more on the requirements and particularly if you moving from another quality system like GMP or ISO 17...

Now that the HIPAA rules have been in place for more than a dozen years, the days of advice and counseling have been replaced by a hard-nosed enforcement attitude, where HHS OCR is ready to make health care organizations that violate the rules feel some pain for their actions, and employer-based health plans are no exception. In order to determine their HIPAA compliance obligations, employers need to go through an analysis of their health insu...

Companies engaged in the conduct of human clinical trials must adhere to specific government regulatory requirements. Certain documents, content and images related to a clinical trial must be stored and maintained, and depending on the regulatory jurisdiction, this body of information may be stored in a trial master file (TMF). The TMF includes all of the documentation that a sponsor must record to demonstrate that they have met their obligati...