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Kincaid, the scientific director of T.M.T.I., told me that a major lesson was that a rapid response to a biological emergency must be accompanied by an equally rapid process for testing and approval.
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For example, countries may allow for testing and regulatory approval of generic versions of drugs before the patent has expired, thereby allowing availability of generics soon after patent expiration.
But the licenses for testing and final commercial approval are granted by a joint-ministerial conference made up of representatives from twelve agencies; it is convened by the Ministry of Agriculture, which is subject to State Council influence and the imperative of maintaining "social stability"—that is, avoiding public unrest.
But the licenses for testing and final commercial approval are granted by a joint-ministerial conference made up of representatives from twelve agencies; it is convened by the Ministry of Agriculture, which is subject to State Council influence and the imperative of maintaining "social stability" — that is, avoiding public unrest.
The description of the potential side effects is, therefore, an important element of the testing and approval procedure for PPPs.
Insurance companies expect to reap enormous savings if they can persuade hundreds of thousands of doctors to use computers and the Internet instead of telephones and paper to submit claims for reimbursement, check on patients' coverage and obtain routine approvals for tests and referrals to specialists.
These could include breast, prostate and liver biopsies, some cardiac procedures, and the precise delivery of radiotherapeutics or anti-cancer drugs to tumours.The system has already undergone successful testing on live, anaesthetised pigs and is now heading for pre-clinical testing and regulatory approval.
The costs of inventing, testing and winning approval for a new drug now average $500m.
This included resource supply failures, time-consuming administrative burdens, delays in receiving laboratory test results and approval for providing oseltamivir to patients, and a lack of clear communication about policy changes as the situation progressed [ 30].
They first announced their desire to release the freak bugs and submitted plans for test dispersions for USFDA review and approval in 2012.
Wait for approval (testing) and repair or replacement.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com