Seminar Information: Imagine not getting paid for your international sale! Unfortunately, it does happen. Learn to fully comply with Letters of Credit requirements to ensure that you receive payment for your shipments. Get involved in the set-up process, learn the basic terminology and significance of various documents, and learn how to prevent and handle discrepancies. Everyone involved in the international sale should learn about the Letters...

Seminar Information: So now that you have learned the Incoterms basics, you want to take this class to learn which term is the best fit for your company and how to maximize your profit! A level II class on the application of Incoterms® Rules in purchases and sales. Course will review the strategy and tactics of negotiating the minimization of landed cost and the maximization of profit from both perspectives purchasing and sales. IMPORTANT...

This hands-on program prepares participants to test and certify systems containing HEPA filtration and gas adsorption systems for nuclear and non-nuclear applications. Participants learn the latest regulatory requirements for nuclear air cleaning, develop an understanding of filtration theory, and gain the experience they need to maintain air purity with a comprehensive filter system. This program offers knowledge and essential hands-on traini...

This continuing education course provides you with the full set of skills needed to integrate occupational health and safety with health promotion programs. You will also learn to implement outcomes measurement programs and to assess the financial impact of integrated employee health programs, gaining the skills to make the business case for improving employee health. During the program, you will develop a roadmap for integrating your company...

Decision makers from business, industry and government must now seek integrated energy solutions — solutions which assure both a secure and affordable power supply, and effective management of both energy and overall operational costs. Globalcon, presented by the Association of Energy Engineers, is designed specifically to facilitate those who need to get up to speed on the latest developments in the energy field, explore promising new t...

Course "Applying ISO14971 and IEC62304 - A guide to practical Risk Management" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Gaps, incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the deve...

Prior to developing a process control plan as part of an overall risk management strategy, process development studies must be completed. The objective of these process development studies is to gain knowledge and understanding about how variation in process parameters explains variation in the product quality characteristics of the product. The use of DOE methodology provides a means to identify process parameters which impact product quality...

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 known to be...

The design and construction of a laboratory, regardless of its use, involves many stakeholders. While providing a safe environment for laboratory users to perform their work is imperative, competing stakeholders’ needs often cause health and safety considerations to be overlooked. Participating in Guidelines for Laboratory Design: Health and Safety Considerations will help you address this issue by providing you with an understanding of...

Course "Analytical Instrument Qualification and Validation: Understanding to Prepare for FDA Audits to become Part 11 Compliant" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: In this two day workshop conference you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process v...