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Technical report series

The Natural Resource Publication Series produces peer reviewed reports that are of interest and use to National Park Service staff, natural resource managers, scientists, and the public. The series has two types of reports, which differ based on the level of analysis and data interpretation, and peer review:. Natural Resource Data series - timely release of basic data sets and data summaries.

A third series, the Natural Resource Technical Report series, was discontinued in See the links below for more information about submitting new reports for publication. Explore This Park. Natural Resource Publication Series.

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The series has two types of reports, which differ based on the level of analysis and data interpretation, and peer review: Natural Resource Report series - information and analysis about natural resources on NPS lands Natural Resource Data series - timely release of basic data sets and data summaries A third series, the Natural Resource Technical Report series, was discontinued in Procedures for Submitting New Reports.

Report Templates. Peer Review. Frequently Asked Questions. For more information, please contact the series manager, Fagan Johnson. Last updated: July 29, Tools Contact Us.The WHO Technical Report Series makes available the findings of various international groups of experts on a broad range of medical and public health subjects. It is governed through rules and procedures that are strictly adhered to.

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ECSPP was established at the first World Health Assembly, into provide recommendations and tools to ensure the quality of medicines: from their development phase to their final distribution to patients.

Guidelines relating to medicines quality assurance are drafted by pharmaceutical specialists, in consultation with the WHO Expert Advisory Panel on The International Pharmacopoeia and Pharmaceutical Preparations, other specialists from industry, national institutions and nongovernmental organizations. Preparation of guidelines generally incorporates an extensive consultative procedure. If considered to be appropriate they are adopted as international standards.

Many of these annexes underpin the procedures and activities of WHO medicines prequalification and therefore serve as valuable references for manufacturers, regulators and procurers. WHO inspections of the manufacturing sites of active pharmaceutical ingredients and finished pharmaceutical products, undertaken as a component of evaluation for WHO prequalification, are based on WHO GMP. The guidelines most relevant to WHO medicines prequalification are listed and accessible below.

Guidelines on submission of documentation for a multisource generic finished product. Prequalification of quality control laboratories.

Procedure for assessing the acceptability, in principle, of quality control laboratories for use by United Nations agencies revised WHO Technical Report Series, No. Guidance on the selection of comparator pharmaceutical products for equivalence assessment of interchangeable multisource generic products WHO Technical Report Series, No.

General guidelines for the establishment, maintenance and distribution of chemical reference substances WHO Technical Report Series, No.

technical report series

Skip to main content. WHO prequalification requirements for active pharmaceutical ingredients and finished pharmaceutical products Guidelines on active pharmaceutical ingredient master file procedure WHO Technical Report Series, No.The table presents an at-a-glance view of report numbers, chemical names, and conclusions.

From the table, click any report number to view the related abstract, click any CASRN to view the testing status page, and click any date to view target organs and levels of evidence. The National Toxicology Program describes the results of individual experiments on a chemical agent and notes the strength of the evidence for conclusions regarding each study. Negative results, in which the study animals do not have a greater incidence of neoplasia than control animals, do not necessarily mean that a chemical is not a carcinogen, inasmuch as the experiments are conducted under a limited set of conditions.

Positive results demonstrate that a chemical is carcinogenic for laboratory animals under the conditions of the study and indicate that exposure to the chemical has the potential for hazard to humans. Other organizations, such as the International Agency for Research on Cancer, assign a strength of evidence for conclusions based on an examination of all available evidence, including animal studies such as those conducted by the NTP, epidemiologic studies, and estimates of exposure.

Thus, the actual determination of risk to humans from chemicals found to be carcinogenic in laboratory animals requires a wider analysis that extends beyond the purview of these studies. Five categories of evidence of carcinogenic activity are used in the Technical Report series to summarize the strength of evidence observed in each experiment: two categories for positive results clear evidence and some evidence ; one category for uncertain findings equivocal evidence ; one category for no observable effects no evidence ; and one category for experiments that cannot be evaluated because of major flaws inadequate study.

Technical report series

These categories of interpretative conclusions were first adopted in June and then revised on March for use in the Technical Report series to incorporate more specifically the concept of actual weight of evidence of carcinogenic activity. For each separate experiment male rats, female rats, male mice, female miceone of the following five categories is selected to describe the findings. These categories refer to the strength of the experimental evidence and not to potency or mechanism.

Clear Evidence of Carcinogenic Activity is demonstrated by studies that are interpreted as showing a dose-related i increase of malignant neoplasms, ii increase of a combination of malignant and benign neoplasms, or iii marked increase of benign neoplasms if there is an indication from this or other studies of the ability of such tumors to progress to malignancy.

Some Evidence of Carcinogenic Activity is demonstrated by studies that are interpreted as showing a chemical-related increased incidence of neoplasms malignant, benign, or combined in which the strength of the response is less than that required for clear evidence. Equivocal Evidence of Carcinogenic Activity is demonstrated by studies that are interpreted as showing a marginal increase of neoplasms that may be chemically related. No Evidence of Carcinogenic Activity is demonstrated by studies that are interpreted as showing no chemical-related increases in malignant or benign neoplasms.

Inadequate Study of Carcinogenic Activity is demonstrated by studies that because of major qualitative or quantitative limitations cannot be interpreted as valid for showing either the presence or absence of carcinogenic activity. For studies showing multiple chemical-related neoplastic effects that if considered individually would be assigned to different levels of evidence categories, the following convention has been adopted to convey completely the study results.

In a study with clear evidence of carcinogenic activity at some tissue sites, other responses that alone might be deemed some evidence are indicated as "were also related" to chemical exposure. In studies with clear or some evidence of carcinogenic activity, other responses that alone might be termed equivocal evidence are indicated as "may have been" related to chemical exposure. When a conclusion statement for a particular experiment is selected, consideration must be given to key factors that would extend the actual boundary of an individual category of evidence.Each webinar will open with a discussion of how flexible building loads can be integrated and controlled to benefit society.

Authors of each report will summarize their key findings and recommendations before listeners will have a unique opportunity to discuss these findings, ask questions, and provide feedback. Through its grid-interactive efficient building GEB research, the U. Department of Energy DOE Building Technologies Office BTO seeks to build on existing energy efficiency efforts and develop technological capabilities to optimize the interplay between building loads and the electric grid.

This webinar will frame issues surrounding the integration of different grid services across different end-uses within a building. We will present several integration options and discuss implications for execution, estimation of demand flexibility and subsequent measurement and verification, and occupant interaction.

Technology-wise, we will focus on whole-building control, sensing, and modeling and address issues like performance, complexity, and cybersecurity. Register here. Skip to main content.This report examines the science base of the relationship between diet and physical activity patterns, and the major nutrition-related chronic diseases. Recommendations are made to help prevent death and disability from these diseases.

These population nutrient intake and physical activity goals should contribute in the development of regional strategies and national guidelines to reduce the burden of nutrition related diseases: obesity, diabetes, cardiovascular disease, several forms of cancer, osteoporosis and dental disease. The recommendations contained in this report are based on the examination and analysis of the best available evidence and the collective judgement of a group of international experts, brought together by WHO and the UN Food and Agriculture Organization FAO.

For queries about the Diet, nutrition and the prevention of chronic diseases expert report or about the Global Strategy.

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Nutrition labels and health claims: the global regulatory environment [pdf kb]. Marketing food to children: the global regulatory environment [pdf kb]. Health Topics. About Us. Skip to main content. Highlight More information. Frequently asked questions Global strategy process and issues Questions and answers.

Press information All Global Strategy press releases Press release archive.Please choose whether or not you want other users to be able to see on your profile that this library is a favorite of yours. Finding libraries that hold this item You may have already requested this item. Please select Ok if you would like to proceed with this request anyway. All rights reserved. Privacy Policy Cookie Notice Terms and Conditions WorldCat is the world's largest library catalog, helping you find library materials online.

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Technical Report Series: biological products: general recommendations

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technical report series

APA 6th ed. Note: Citations are based on reference standards.

technical report series

However, formatting rules can vary widely between applications and fields of interest or study. The specific requirements or preferences of your reviewing publisher, classroom teacher, institution or organization should be applied. The E-mail Address es field is required. Please enter recipient e-mail address es. The E-mail Address es you entered is are not in a valid format.Federal government websites often end in. The site is secure. To find a specific report, search the NIST Research Library catalog or view a full list of publications that are available electronically.

The series presents research results, test methods, and performance criteria related to the structural and environmental functions and the durability and safety characteristics of building elements and systems. Share Facebook.

Papers cover a broad range of subjects, with major emphasis on measurement methodology and the basic technology underlying standardization. Technical Report Series Advanced Manufacturing Series AMS — The Advanced Manufacturing Series consists of reports, guides, recommendations, specifications, use cases, and data management methods related to the design, planning, implementation and operation of advanced manufacturing. Topics cover, but are not limited to, additive manufacturing, advanced composites, digital manufacturing, flexible hybrid electronics, integrated photonics, lightweight metals, and smart manufacturing.

Includes current Final and Draft papers. Data Collection Instruments and Best Practices— Publications in this series are targeted towards best practices for collection of qualitative and quantitative data in studies of disasters, failures, and community resilience, these data collection instruments, protocols, and guidance documents are based on extensive experience of NIST researchers across disciplines.

Data collection instruments include questionnaires or survey instruments, interview guides, and other structured means of collecting data. Some of these instruments are designed for human subjects research focused on households, social institutions, and businesses. These analysis briefs often accompany in-depth economic research and facilitate the usage of this analysis by NIST and stakeholders throughout the science and technology transfer policy communities.

As such, a key aim of these Briefs is to communicate economic results in an accessible and non-technical manner. Topics frequently include: economic rationales for government science; characterization and measurement of market failures; economic impact studies; strategic planning studies.

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It is used when the technical project officer decides that a contract report has sufficient technical merit to be made publicly available. Handbooks HB — Recommended codes of engineering and industrial practice including safety codes developed in cooperation with interested industries, professional organizations, and regulatory bodies. National Standard Reference Data Series NSRDS — Provides quantitative data on the physical and chemical properties of materials, compiled from the world's literature and critically evaluated.

Technical Notes TN — Studies or reports which are complete in themselves but restrictive in their treatment of a subject. Analogous to monographs but not so comprehensive in scope or definitive in treatment of the subject area. Topics cover, but are not limited to: non-empirical research results, case studies, posters, charts, best practices, general knowledge, success stories, data sets, and conference summaries. This brief may be used to formally discuss any technology transfer mechanism without the requirement of formal statistical, economic, or econometric analysis.

The predictions series was initially restricted and available only to the military as a basic supplement to the IRPL's "Radio Propagation Handbook" issued by the military. Predictions were made three months in advance.

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