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Best Practices / Guidelines
This framework introduces a risk-based oversight and management methodology for clinical trials. It combines a stratified approach that is based on the marketing authorisation status of the medical product and can be applied in a common manner across countries’ regulatory frameworks, with a trial-specific approach that considers other issues such as the type of populations concerned by the trial, or the informed consent of the patients.
This revised document supplies basic information (compositional considerations, key constituents), useful in risk/safety assessment of food and feed using new varieties of soybean (Glycine max.). This updated publication replaces the original issue of 2001.
This Biosafety Document is intended to supply basic information (biology mainly), useful in environmental risk/safety assessment. Agriculture plant species of Brassica genus are cropped worldwide as oilseeds, vegetables and for other uses.
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This guide comprises eight key points for planning public engagement activities. It contains a set of questions to help policy makers develop a plan from start to finish, as well as practical case studies from countries that have used the guide in their communication activities.
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This Global Science Forum report and its annexed survey analysis identify the existing tools and strategies for urban modelling and their current limitations, and propose a series of policy recommendations aimed at improving the effectiveness and use of urban models.
This guide provides the statistical definitions, classifications and methods to measure and compare the information society across countries. It provides a standard reference for statisticians, analysts and policy-makers in the field.
The Recommendation seeks to assist both OECD member and non-member countries in the development of appropriate sustainability assessment methodologies for bio-based products.
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The aim of these guidelines is to propose a harmonised approach for the collection and analysis of biotechnology research and development (R&D) statistics in the government and higher education sectors.
The ability to effectively use these vast amounts of knowledge will depend in part on the bringing together of different strands of information, data and biological materials within human biobanks and genetic research databases (HBGRDs).
OECD’s Working Party on Manufactured Nanomaterials (WPMN) launched a Sponsorship Programme in November 2007. The programme involves OECD member countries, as well as some non-member economies and other stakeholders to pool expertise and to fund the safety testing of specific Manufactured Nanomaterials (MNs). In launching this Sponsorship Programme, the WPMN agreed on a priority list of 13 MNs for testing (based on materials which are