The phrase "approved was designed to" is not correct in written English.
It seems to be a fragment and lacks clarity without additional context.
Example: "The new software approved was designed to improve efficiency in the workplace."
Alternatives: "authorized was intended to" or "sanctioned was created to".
Consistent with this suggestion, each of the checkpoint programs that we have approved was designed primarily to serve purposes closely related to the problems of policing the border or the necessity of ensuring roadway safety.
The data Merck released Thursday involved patients who had taken Vioxx as part of a clinical trial called Approve, which was designed to determine whether Vioxx — a painkiller approved for arthritis relief — could prevent colon polyps.
Other Enron employees told the committee that Mr. Skilling, then Enron's president and chief executive, "both approved a transaction that was designed to conceal substantial losses" and "withheld from the board important information about that transaction".
"Although Skilling denies it, if the account of other Enron employees is accurate, Skilling both approved a transaction that was designed to conceal substantial losses in Enron's merchant investments and withheld from the board important information about that transaction," the report says.
The consent form, which was approved by the IRB, was designed to be at an acceptable reading level for this study population; it was a two-page form that contained an explanation of the study aims, procedures, etc., including the advanced behavior management techniques that would be assigned in the randomization process (Table 1).
Chidamide is a novel histone deacetylase inhibitor (HDACi) approved in clinical practice that was designed to increase the acetylation level of histone H3.
The proposed breakup, which must be approved by News Corp. shareholders, was designed to mollify investors, who long have been sour on Murdoch's newspaper holdings.
All manipulations with animals were conducted in humane manner, in strict adherence with a protocol approved by institutional ACUC, which was designed to minimize animal suffering.
This ethics approved, prospective single cohort feasibility study was designed to evaluate the dosimetry and toxicity of CBRT using an intensity-modulated radiotherapy (IMRT) technique, compared with a standard sequential boost technique (SBT).
Driven by the positive outcome of the mouse experiments, an open-label phase II pilot study (EudraCT number #2013-001258-82 approved by Local Ethics Committee, protocol reference #85/13) was designed to test the efficacy or the combinatory treatment with cysteamine and EGCG in 10 Caucasian CF patients homozygous for the F508del-CFTR mutation (Table 1 and 2 ).
