Sentence examples for described in guidance from inspiring English sources

OECD validation criteria are described in Guidance Document 34 (GD34; OECD 2005a), which addresses the validation and regulatory acceptance of new or updated test methods for hazard characterization.

On May 4 , 2001 the FDA issued a letter decision in which it declared that it would not authorize Plaintiffs' Antioxidant Vitamin Claim given the agency's review of new antioxidant vitamin/cancer relationship studies under the "significant scientific agreement" standard described in the Guidance Report.

The methods of technology appraisal are described in the "Guidance for Manufacturers and Sponsors.

By following the stepwise procedure and kinetic models described in FOCUS Guidance on Estimating Persistence and Degradation Kinetics [47], the dissipation half-lives of M1 in water and sediment in both systems were estimated as well above 200 days each.

The same principles described in the guidance may be applied to pre- and post-approval changes.

The amount of information available on each event was limited, and the WHO Annex 2 decision instrument criteria described in the guidance were rigidly applied.

The influence of roles and communication on decisions is subtle, varies between cases, and is not described in existing guidance and recommendations.

When guideline neurotoxicity studies are conducted, more detailed tests of nervous system function are possible (as described in OECD Guidance Document for Neurotoxicity Testing (2004), but are seldom conducted in practice.

All test substances were characterized in detail in accordance with the physico-chemical endpoints described in the guidance on information requirements for nanomaterials (ECHA 2012) to EU regulation No. 1907/2006 on the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH; Anon 2006).

The methods used to estimate exposures to polyols are intended to be consistent with the EFSA approach for food additives described in the Guidance for Submission for Food Additive Evaluations of the European Food Safety Authority (EFSA) Panel on Food Additives and Nutrient Sources Added to Food (ANS) (EFSA 2012a).

Because electronic PRO data (including data gathered by personal digital assistants or phone-based interactive voice recording systems) are part of the case history, the FDA expects electronic PRO data to be consistent with the data standards described in that guidance.