premarketing

premarketing

(priːˈmɑːkɪtɪŋ)
adj
before the development of a market
References in periodicals archive ?
The testing is valuable to the current study design and the follow-on premarketing process.
This testing is valuable to the current study design as well as the follow-on premarketing process.
In this position, he provided leadership and program guidance to the staff engaged in Chemistry, Manufacturing and Control (CMC) reviews and GMP inspections for premarketing license applications and post marketing changes of the biological products.
The working group called for a systematic premarketing and postapproval evaluation of CGM system performance, as well as greater investment in clinical trials, including head-to-head comparisons and large independent registry studies.
Corbion has been premarketing new PLA grades in North America since last year, among them a range of high-heat, high-performance cross-linked PLA homopolymer resins--PLLA & PDLA, targeted specifically for applications requiring durability and/or high heat resistance.
The following findings are based on the short-term, placebo-controlled premarketing studies for schizophrenia in which LATUDA was administered at daily doses ranging from 20 to 160 mg (n=1508).
Directs and leads efforts for PM support and consultative services on behalf of manufacturers and subcontracted by third-party consultancies and provides services involving all phases of the product development, submission, and commercialization process from premarketing to postmarketing; retained as U.
Evaluation of real-time effectiveness of the drug and availability of a facility to conduct trials in state-of-the-art settings, thus complementing the outcomes of premarketing randomised control trials, are the prime benefits availed from pharmacovigilance in phase IV trials.
This open session provided an overview of the routine liver function test results used to gauge a drug's potential for causing DILI and reviewed the Food and Drug Administration (FDA) guidance on premarketing clinical evaluation of potential DILI cases (www.
As a starting point, [sec] 273 does specify certain conduct that qualifies as commercial; this includes premarketing regulatory review activities performed to establish the safety or efficacy of the subject matter and nonprofit laboratory use effected for the public benefit.
As a starting point, A* 273 does specify certain conduct that qualifies as commercial; this includes premarketing regulatory review activities performed to establish the safety or efficacy of the subject matter and nonprofit laboratory use effected for the public benefit.
It does appear that the agency intends high-risk LDTs to undergo internal review of their Premarketing Applications, which is the most stringent type of device marketing application required by the FDA.