Examples of 'drug application' in a sentence
Meaning of "drug application"
Drug application can refer to the process wherein a medication or treatment is applied or administered to a patient. It can involve various methods such as oral ingestion, injection, topical application, or inhalation, depending on the type and form of the drug
How to use "drug application" in a sentence
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drug application
Deficiency in medical diagnostics and drug application.
A single drug application was ineffective.
Treatment of tumors by means of drug application.
See new drug application.
This is often required as a part of a new drug application.
Investigational new drug application to have been.
Specific instructions and individual variations of drug application.
Solution changes and drug application with a local perfusion system.
F is defined as an average of five baseline values before drug application.
Full new drug application containing the same active drug ingredient or.
Three products of biotechnology solely used in a food and drug application.
The exceptions are cases of over dosage or drug application after the recommendation course.
There were four multiple dose trials included in the new drug application.
The FDA works with the sponsor of the drug application to expedite the approval process.
Test compounds are added on top of the cells to mimic topical drug application.
See also
Animal drug application for entry in the Register Livestock farm on the island of Formentera.
In individual cases neuropathy can evolve even after a single drug application.
After this stage, a new drug application is submitted.
A test compound is added on top of the cells to mimic topical drug application.
The rate of bath solution exchange and drug application is preferably about 6 ml / min.
The adverse dermatological events occur in the tissue around the area of drug application.
The drug application is synchronized with data acquisition by using a 2-way electronic valve.
During FDA review of the investigational new drug application.
Monitoring device for drug application with a drug pen, with logging, communication and alarms.
New drugs receive extensive scrutiny before FDA approval in a process called a new drug application NDA.
Tasigna supplemental New Drug Application ( sNDA ) was accepted by FDA and granted priority review.
This trial took place under an Investigational New Drug application.
Cipher CIP-Isotretinoin new drug application accepted for review Cipher Pharmaceuticals Inc.
The improvement in erythema was maintained for at least 7 days after discontinuation of drug application.
The decision was based on the supplemental New Drug Application submitted by AstraZeneca.
New Drug Application submission is based on the MONARCH 1 and MONARCH 2 studies.
Thus, the effectiveness of prior art methods of topical drug application is often limited.
AbbVie is targeting a 2017 New Drug Application filing with the FDA for elagolix in endometriosis.
Nonetheless, they have been applied in only a few cases of actual new drug application.
Investigational new drug application ( IND ) became effective.
Sanofi 's decision was not related to safety issues or deficiencies in the New Drug Application.
It 's covered under an investigational new drug application ( IND ) that 's reviewed by the FDA.
There were 10 single dose analgesia trials included in the new drug application.
The investigational new drug application was withdrawn by the manufacturer in 1999, citing safety concerns.
The mean contraction force in a period of 2 min before drug application was taken as pre-value.
Approved new drug application under the ( FDCA ) Federal Food, Drug, and Cosmetic Act ; or.
Regulatory filings / consultant fees for New Drug Application.
Sandoz filed its abbreviated new drug application for generic enoxaparin in August 2005.
A supplement number is associated with an existing FDA New Drug Application ( NDA ) number.
It plans to submit a new drug application to the Food and Drug Administration in 2016.
Submission and approval of a new drug application ( NDA ).
In 2009, the FDA began fast-tracking the new drug application of iniparib for triple-negative breast cancer.
Finally, a year later, the FDA has now accepted the drug application.
It is anticipated that a New Drug Application will be filed with the FDA in mid-2014.
Generally, the FDA takes between 6 and 12 months to review and rule on a drug application.
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