regulatory testing
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2021 ◽  
Vol 9 (02) ◽  
pp. 451-452
Author(s):  
Antonio Villanueva

Health regulatory authorities worldwide are tasked with approving drugs, medical devices, and vaccines to ensure their safety, efficacy, and quality for public use. Significantly over the past three decades, testing of these products has witnessed increasingly stringent tests due to advancing scientific knowledge and technology. Specifically, the relatively new field of studies on the human gut microbiome and its interactions with drugs and vaccines may accumulate enough evidence in the future to justify its testing prior to regulatory approval or during post-marketing surveillance.


Author(s):  
Peter J. Sakalaukus ◽  
Nathan P. Barrett ◽  
Brian J. Koeppel

Abstract The Pacific Northwest National Laboratory (PNNL) is the design authority for a new Type B hazardous materials transportation package designated as the Defense Programs Package 3 (DPP-3) for the U.S. Department of Energy (DOE) National Nuclear Security Administration (NNSA). The DPP-3 has been developed using similar materials and fabrication methods employed in previous U.S. Nuclear Regulatory Commission (NRC), DOE, and NNSA certified packages. The DPP-3 design criteria are derived from the American Society of Mechanical Engineers (ASME) Boiler and Pressure Vessel Code (BPVC), NNSA guidance and NRC regulatory guides in order to safely and securely transport a variety of payloads. Final regulatory approval by the NNSA will require regulatory testing to demonstrate that the containment vessel (CV) remains leaktight after enduring the entire regulatory testing sequence prescribed in Title 10 of the Code of Federal Regulations Part 71 (10 CFR 71). In order to gain confidence that the DPP-3 will remain leaktight after testing, the DPP-3 has been structurally analyzed using the Finite Element Analysis (FEA) software LS-DYNA. The FEA analyses serve two general purposes: first, they aid in design and development of the package, and second, they advise as to which drop orientations are expected to cause the most damage during regulatory testing. This paper will discuss how the design criteria are incorporated into analytical techniques needed to evaluate the FEA structural simulation results for 10 CFR 71 conditions to give confidence the DPP-3 testing campaign will be successful.


Chemosphere ◽  
2020 ◽  
Vol 240 ◽  
pp. 124943 ◽  
Author(s):  
James R. Wheeler ◽  
Helmut Segner ◽  
Lennart Weltje ◽  
Thomas H. Hutchinson

2019 ◽  
Vol 102 (6) ◽  
pp. 1756-1766
Author(s):  
Jennifer Bates ◽  
Adilah Bahadoor ◽  
Yi Cui ◽  
Juris Meija ◽  
Anthony Windust ◽  
...  

Abstract Background: Among the regulated mycotoxins that contaminate global food supplies, ochratoxin A is particularly harmful as a nephrotoxin and suspected carcinogen. Objective: To support global measurement comparability, certified calibration solutions for ochratoxin A and [13C6]-ochratoxin A (OTAN-1 and OTAL-1, respectively) as well as a mycotoxin-contaminated rye flour certified reference material (CRM) known as MYCO-1 were developed. Methods: Quantitative proton NMR was used along with maleic acid as an external standard traceable to the Système international (SI) to measure the concentration of ochratoxin A and [13C6]-ochratoxin A for the calibration solutions. OTAN-1 and OTAL-1 were then used as a pair in double isotope dilution MS to certify the mass fraction of ochratoxin A in MYCO-1. The natural ochratoxin A CRM served as the primary standard for traceable quantitation, while the synthetic [13C6]-ochratoxin A CRM served as the internal standard. Results: The certified mass fraction of ochratoxin A or [13C6]-ochratoxin A in the two mycotoxin calibration solution standards was established to be 11.03 ± 0.32 µg/g (k = 2) for OTAN-1 and 4.89 ± 0.18 µg/g (k = 2) for OTAL-1. The mass fraction of ochratoxin A in the rye flour standard MYCO-1 was certified at 4.05 ± 0.88 µg/kg (k = 2). Conclusions: These CRMs will support regulatory testing as they can be used in the method development, validation, calibration, and QC analysis of ochratoxin A. Highlights: This report highlights the methods used to certify OTAN-1, OTAL-1, and MYCO-1 as well as the challenges associated with producing such materials, which can be applied to a wide variety of other CRMs.


2019 ◽  
Vol 102 (6) ◽  
pp. 1756-1766 ◽  
Author(s):  
Jennifer Bates ◽  
Adilah Bahadoor ◽  
Yi Cui ◽  
Juris Meija ◽  
Anthony Windust ◽  
...  

Background: Among the regulated mycotoxins that contaminate global food supplies, ochratoxin A is particularly harmful as a nephrotoxin and suspected carcinogen. Objective: To support global measurement comparability, certified calibration solutions for ochratoxin A and [13C6]-ochratoxin A (OTAN-1 and OTAL-1, respectively) as well as a mycotoxin-contaminated rye flour certified reference material (CRM) known as MYCO-1 were developed. Methods: Quantitative proton NMR was used along with maleic acid as an external standard traceable to the Système international (SI) to measure the concentration of ochratoxin A and [13C6]-ochratoxin A for the calibration solutions. OTAN-1 and OTAL-1 were then used as a pair in double isotope dilution MS to certify the mass fraction of ochratoxin A in MYCO-1. The natural ochratoxin A CRM served as the primary standard for traceable quantitation, while the synthetic [13C6]-ochratoxin A CRM served as the internal standard. Results: The certified mass fraction of ochratoxin A or [13C6]-ochratoxin A in the two mycotoxin calibration solution standards was established to be 11.03 ± 0.32 µg/g (k = 2) for OTAN-1 and 4.89 ± 0.18 µg/g (k = 2) for OTAL-1. The mass fraction of ochratoxin A in the rye flour standard MYCO-1 was certified at 4.05 ± 0.88 µg/kg (k = 2). Conclusions: These CRMs will support regulatory testing as they can be used in the method development, validation, calibration, and QC analysis of ochratoxin A. Highlights: This report highlights the methods used to certify OTAN-1, OTAL-1, and MYCO-1 as well as the challenges associated with producing such materials, which can be applied to a wide variety of other CRMs.


Author(s):  
Joshua P. Flach ◽  
Paul S. Blanton

Abstract Structural honeycomb is widely used as both an impact limiter and rigid structural support in applications which require a high specific strength and highly characterized energy absorption profile. Structural honeycomb is an anisotropic material with limited strength in directions perpendicular to the cells and features mechanical properties that are largely driven by the materials of construction and structure density. As a result, the mechanical properties of honeycomb are sensitive to the specific geometry, orientation, and reinforcement of the honeycomb structure. This study evaluates the effects of these characteristics on stainless steel structural honeycomb to account for the complex loading conditions experienced during radioactive material package regulatory testing. This material is intended for use in applications where organically bonded honeycomb cannot be used.


2019 ◽  
Vol 104 ◽  
pp. 74-83 ◽  
Author(s):  
Kirsten Rasmussen ◽  
Hubert Rauscher ◽  
Peter Kearns ◽  
Mar González ◽  
Juan Riego Sintes
Keyword(s):  

2018 ◽  
Vol 296 ◽  
pp. 10-22 ◽  
Author(s):  
Peter Day ◽  
Richard M. Green ◽  
Melanie Gross ◽  
Lennart Weltje ◽  
James R. Wheeler

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