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This course is verified by Probitas Authentication as meeting the AS9104/3A requirements for continuing Professional Development. This one-day program is designed to provide introductory information for those organizations who are considering transitioning from the Aeronautic, Space and Defense industry to the Food & Drug Administration (FDA), Medical Device Manufacturing market. Reviewing essential information necessary to understand and successfully begin the journey to FDA Medical Device approval, this course will examine many of the controls between the AS9100 Standard and FDA Regulations and identify the similarities.

The Manufacturing Message Specification is an application layer Standard designed to support messaging communications to and from programmable devices in a Computer Integrated Manufacturing (CIM) environment. This environment is referred to in this Standard as the manufacturing environment. This Standard does not specify a complete set of services for remote programming of devices, although provision of such a set of services may be the subject of future standardization efforts.

The presentation provides an overview about the activities of Eurocae Working Group 72 (WG-72) starting with a brief synopsis of the context which suggested why such a committee should be established in 2006. It then goes into further detail about the drivers for the work of the committee, which call for the products to be delivered. It addresses some of the challenges with respect to its users. It points out that one of the lessons the committee learned was importance of the focus on the users, such that the products provide their maximum utility. Hence, the users should better be among the participants to achieve this objective. Other industries have dealt with the subject of Information System (or Cyber-Physical) Security long before this industry was forced to consider it. Consequently there are many industry standards and national or international norms, which may help to develop what is deemed needed for Civil Aviation.

Alyson Lyon, Executive Leadership Coach, explains what stress is, and how to handle personally and professionally. SAE Members can view the full version by logging into the Member Connection. Not a Member? Join us today at sae.org/join.

Abstract Sleep quality and maintenance of the optimal cognitive functioning is of crucial importance for aviation safety. Fatigue Risk Management (FRM) enables the operator to achieve the objectives set in their safety and FRM policies. As in any other risk management cycle, the FRM value can be realized by deploying suitable tools that aid robust decision-making. For the purposes of our article, we focus on fatigue hazard identification to explore the possible developments forward through the enhancement of objective tools in air transport operators. To this end we compare subjective and objective tools that could be employed by an FRM system. Specifically, we focus on an exploratory survey on 120 pilots and the analysis of 250 fatigue reports that are compared with objective fatigue assessment based on the polysomnographic (PSG) and neurocognitive assessment of three experimental cases.

The CDIF Family of Standards is primarily designed to be used as a description of a mechanism for transferring information between CASE tools. It facilitates a successful transfer when the authors of the importing and exporting tools have nothing in common except an agreement to conform to CDIF. The language that is defined for the Transfer Format also has applicability as a general language for Import/Export from repositories. The CDIF Integrated Meta-model defined for CASE also has applicability as the basis of standard definitions for use in repositories. The standards that form the complete family of CDIF Standards are documented in EIA/IS-106 CDIF - CASE Data Interchange Format - Overview. These standards cover the overall framework, the transfer format and the CDIF Integrated Meta-model. The diagram in Figure 1 depicts the various standards that comprise the CDIF Family of Standards. The shaded box depicts this Standard and its position in the CDIF Family of Standards.

This specification covers resin-bonded glass fibers in the form of felted pads, flat or in rolls.

This specification covers resin-bonded glass fibers in the form of felted pads, flat or in rolls.

This specification covers resin-bonded glass fibers in the form of felted pads, flat or in rolls.

This specification and its supplementary detail specifications cover continuous multifilament carbon tow woven into fabric and impregnated with uncured resin.

This specification and its supplementary detail specifications cover continuous multifilament carbon tow woven into fabric and impregnated with uncured resin.

This specification and its supplementary detail specifications cover rigid, cellular polyurethane or polyisocyanurate (polyether only) foam in the form of board or block.

This specification and its supplementary detail specifications cover rigid, cellular polyurethane or polyisocyanurate (polyether only) foam in the form of board or block.

This specification covers paper base honeycomb material having a cell size of 0.440 in. (11.18 mm). Unless otherwise ordered, size 0.440 in. (11.18 mm) will be supplied.

This specification covers paper base honeycomb material having a cell size of 0.440 in. (11.18 mm). Unless otherwise ordered, size 0.440 in. (11.18 mm) will be supplied.

This specification and its supplementary detail specifications cover rigid, cellular polyurethane or polyisocyanurate (polyether only) foam in the form of board or block.

This specification covers a modified epoxy adhesive in the form of supported film supplied in rolls or sheets.