Examples of using Draft guidance in English and their translations into Danish
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Medicine
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Colloquial
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Official
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Financial
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Ecclesiastic
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Official/political
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Computer
Draft guidance issued for comment.
CDRH appeals processes: final and draft guidance released.
Draft guidance on HUD designations.
Latex free' labelling to be replaced under new draft guidance.
Draft guidance on FDA decisions for IDEs.
FDA decisions for IDE clinical investigations: draft guidance.
Draft guidance circulated for comment.
Providing early feedback on device submissions: draft guidance.
Draft guidance: contemporary perspective on 510(k) process.
Determination of administrative completeness of a PMA: draft guidance.
Draft guidance on standardising electronic study data.
See the client update on the new standard and draft guidance March 2014.
CDRH appeals: draft guidance clarifies available processes.
Molecular diagnostic instruments with combined functions: draft guidance.
Draft guidance on paediatric uses of x-ray imaging devices.
Device reporting for manufacturers:comments sought on draft guidance.
Draft guidance to improve representation of women in clinical studies.
Blood glucose test systems:extension of comment period on draft guidances.
Draft guidance on transferring to another Institutional Review Board.
Artificial pancreas system clinical trials and product approvals: draft guidance.
Draft guidance: 510(k)s for small-bore connectors used in enteral applications.
Post-approval modifications to a combination product: draft guidance issued.
US seeks feedback on draft guidance for bipolar electrosurgical vessel sealers for general surgery.
Endotoxin testing recommendations for single-use IODs: draft guidance issued for comment.
At that time, in 1989, the cut-off values for the level of renal impairment were in line with FDA draft Guidance for Industry on“ Pharmacokinetics and Pharmacodynamics in patients with Impaired renal function: study design, data analysis, and impact on dosing and labelling”.
AHWP drafts guidance for medical device distributors on QMSs.
Feedback sought on draft cybersecurity guidance.
Non-conformity grading system for regulatory audits: draft GHTF guidance.
Public consultation held on draft US guidance concerning medical devices containing animal-derived material.
Guidance drafted on certain IRB responsibilities.