Course: "The A to Z's of Microbial Control, Monitoring, Validation and Troubleshooting of Pharmaceutical Water Systems” 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 provide a microbiology-focused education about all aspects of water systems and how biofilm manages to thrive there. Prior microbiological education or tra...

Information security training in Seattle from SANS Institute, the global leader in Cyber Security training. At SANS Seattle 2015, SANS offers hands-on, immersion-style security training courses taught by real-world practitioners and leading experts working in security today.The site of SANS Seattle 2015, October 5 - 10, is the Renaissance Seattle Hotel, located just minutes from Pike Place Market and upscale shopping, with stunning views of Pu...

Overview: Drug development is the process of incorporating data from multiple disciplines into a logical and coherent argument for the efficacy and safety of a drug product resulting in regulatory approval. The course will focus on the clinical aspect. The primary goal of the course will provide students with the basic principles and process for taking a chemical and developing it into a drug product. Medical, pharmaceutical, pharmacokinetics,...

Don't let your company become a liability; understand the employee's rights and employer's responsibilities on military leave. As a result of the continuing global war on terrorism, employers are faced with an unprecedented level of impact of military service on the workplace. What must an employer do when an employee gets orders to be activated? Do you have to hold the job open? What if it's an employee's family member with the orders - what...

According to IDC, outdated federal IT networks are incapable of fully exploiting the extensive advantages of the mobility, cloud, social networking, and big data analytics technologies collectively. This modern infrastructure will allow agencies to develop flexible networks that can easily and cost-effectively adapt to the changing needs of federal employees, citizens, and warfighters. Agencies are holding back because of concerns that moderni...

Capability Statements may be your most important marketing tool. An effectiveCapability Statement can open doors to over $500 billion dollars that will be won in government contracts. Unfortunately, most contractors make the huge mistake of taking the “one size fits all” approach by providing the same generic Capability Statement for every opportunity. Attend this class virtually or in-person at our new office. Do you know how to e...

This course, led by senior NTSB management and investigators, details how the Safety Board investigates major aircraft accidents and what it expects of participants in an investigation. Upon completion of this course the participant will: Improve the overall preparedness of an airline response team Reduce confusion following an accident event by proactively managing the on-scene situation Explain the role of the air carrier as a part of the ...

A variety of five qualitative and quantitative methodologies are discussed in detail during this three-day workshop. The “do’s & don’t” of report writing are covered. Field evaluations are conducted. Students will learn the differences between qualitative and quantitative risk analysis. They will use a variety of methodologies by evaluating single or multiple buildings and critical infrastructure nodes. This worksho...

Export Administration Regulations (EAR), International Traffic in Arms Regulations (ITAR) and Office of Foreign Assets Controls & Embargoes (OFAC) Explained - complete with the latest updates on Export Control Reform (ECR) as they apply to NON-US COMPANIES: This seminar series provides both novice and experienced export compliance professionals with an in-depth education on export control regulations administered by the US Departments of...

Overview: Analytical equipment should be qualified and computer systems should be validated to demonstrate suitability for the intended use. Electronic records must comply with FDA Part 11 and EU/PICS GMP Annex 11 requirements to ensure data integrity, security and availability. Recent EU and FDA inspection documents prove that qualification, validation and electronic laboratory are records are on target of inspectors. The large number of warn...