FDA General Principles of Software Vali...
Course "FDA's Software Monsters: Cybersecurity, Interoperability, Mobile Apps and Home Use" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Software's level of complexity and use is expanding at exponential levels. Likewise, the potential risks to health follow suit. Ransomeware attacks hold your software hostage until you pay hundreds or thousands of do...
What is the HIPAA Compliance | HIPAA Pr...
Overview: This two-day seminar takes the participants through HIPAA compliance from start to compliance. The first presentation explains the history of HIPAA, why it came to being and its evolution. This covers what HIPAA is, what steps have to be performed to be HIPAA compliant and what HIPAA compliance is. It also provides definitions to key HIPAA terms, how to define a Business Associate and how to contract with Business Associates. The sec...
What is Project Management in Pharmaceu...
Course "Risk Based Project Management for the Life Sciences Industry" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Project management is a discipline that can be applied to all industries. In the pharmaceutical industry, project management is the key to addressing the unique regulatory, compliance and quality related needs of the industry. The process...
FedInsider Defense Health IT Summit
Over the next four to six years, healthcare organizations will find themselves in the midst of a shift in the way that healthcare is administered and monitored. According to research, patients will begin taking ownership of their healthcare which will create a deep ripple effect across IT networks that enable the day-to-day activities of the military. To address these seismic changes, the military is looking at how technology solutions will su...
May 16, 2017
Organizer:
FEDINSIDER Location:
San Diego, CA
Statistics for the Non-Statistician
Statistical tools and techniques are very commonly used to help measure and improve the quality of a firm's process and product. If statistical analysis is not properly performed and/or understood, a firm can run the risk of distributing the kind of product to the market that ultimately fails, resulting in lost time and money. And of course, with statistics, practice makes perfect. During this two-day HIGHLY interactive training program, parti...
Best Practices for FDA Inspection 2016
Overview: Many regulated companies preparing for FDA inspections are not prepared and the outcome can be negative as we see all the time with enforcement actions. This seminar provides the fundamentals and the ground rules on how to prepare for and survive an FDA inspection no matter if you are a Class I, II, III device or a pharmaceutical or biologics manufacturer. This presentation will review and emphasize the do's and don'ts and cardinal r...
Process Validation and Development 2016
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. Overview: 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 e...
Risk Management in Medical Device Design 2016
Overview: Design Controls are essential for producing safe and effective medical devices. And Design Controls are considered a critical process by the FDA. Yet is still one of the most frequent areas for 483 and Warning Letter observations. This 2 days seminar will help you understand and develop design controls processes and tools that are a competitive strength for your company. Intrinsic quality, safety, and effectiveness of a device are kn...
Medical Devices Compliance 2016 in USA
Overview: Have you had the experience of guiding a new product through concept, development, and final design, and, while you are preparing the product for US introduction, you suddenly stop dead. It seems FDA has decided your product is a medical device! The basic definition of a medical device is extremely broad, including "instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent, or other similar or related article,...
Best Practices for Setting Up a Durable...
Increased Revenue & Profit For Your Practice! Better Service & Outcomes For Your Patients From Your Existing Patient Base! This seminar will provide you with the following critical information and materials: How to develop Profits $5,000-$20,000+ Per Month, Per Doctor though Durable Medical Equipment (with but a few patients a week or day) How to Become Immediate Positive Cash-Flow How to provide a "Convenient One-Stop Medical Shopping...
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