In an effort to support resiliency and keep risk management efforts focused on local port activites, the U.S. Department of Homeland Security, in partnership with State, local, and regional stakeholders, is proud to announce the Delaware River Ports Supply Chain Security and Resilience Workshop. This event is open to: Facility and terminal operators; Utilities; Neighboring ports; OEMs; Security professionals from the private and public sectors...

Course "Risk Analysis and Design of Experiments (DOE) in Process Validation and Development" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. GlobalCompliancePanel Refer a Friend Program: Any Customer to 3 Referrals "Can Participate 2 Days Seminar for free of Cost Overview: This course is designed to help scientists and engineers plan and conduct experiments and an...

This course is designed to help scientists and engineers plan and conduct experiments and analyze the data to develop predictive models used to optimize processes and products and solve complex problems. DOE is an extremely efficient method to understand which variables (and interactions) affect key outcomes and allows the development of mathematical models used to optimize process and product performance. The models also provide an understand...

Overview:Writing SOPs or procedural documents can be challenging at times. However, writing SOPs is overall a straightforward process. However, enforcing what you already created and implemented in the pipeline is another story. The term SOP is very obvious. We have seen "clearly written description of how specific tasks are to be done." Another satisfactory definition would be "detailed written instructions that achieve the uniformity of the...

This will be an all-inclusive class that give details on understanding the laws such as FLSA and other laws such as the portal to portal act that help payroll professionals determine proper pay methods. Once the correct pay method is determined this class will give the skills to understand how to properly calculate overtime pay accurately according to FLSA guidelines for all types of payrolls. The assist in the learning process case studies wi...

This course covers a very broad range of topics from worker classification, to employee classification, to establishing methods and rates of pay, what must be included in the rate of pay, hours that must be compensated as worked time, required benefits, de minimus working fringes, withholdings and deductions from pay, voluntary deductions, child support and garnishment orders, payroll reporting, analysis of risks of noncompliance, proper docum...

We are pleased to invite you to attend our new event in Pennsylvania with SANS Philadelphia 2016 on February 29 - March 5 at the Sonesta Philadelphia, located in downtown Philadelphia.We have five of our top information security courses selected to provide you with the training and certification that you need to boost your career by learning from the best! SANS Instructors are industry professionals who will ensure that you not only learn the...

Stem Cell Therapy-2016 has the goal to fulfill the prevailing gaps in the transformation of this science of hope, to serve promptly with solutions to all in the need. World Congress Stem Cell Therapy 2016 will have an anticipated participation of 300+ delegates across the world to discuss the conference goal. Success Story: Cell Science Conference Series The success of the 5th Cell Science conference series has given us the prospect to bring t...

2nd International Conference on Smart Materials & Structures "welcome all" to the Grand Three Day's Scientific Event on Smart Materials and Intelligent Structures held from Feb 29-March 02, 2016 at Philadelphia, USA. Smart Materials 2016 with the theme “Exploring Intelligence with Smart Material Structures” and aims in promulgating knowledge and facilitates to share experimental and current research experiences and outcomes amo...

Course "Regulatory Affairs aspects of clinical trials and clinical Product Development in the EU" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: The main document from a regulatory perspective in the development of a medicinal product is the regulatory plan. In this Seminar it is explained how to write the regulatory plan, and which aspects to consider....