Sentence examples for Approval submissions from inspiring English sources

The fatigue resistance of UHMWPE is now widely accepted as critical to the structural performance of orthopedic implant bearings, and such data are now commonplace in regulatory approval submissions.

In addition, although not reported in the published scientific literature, FDA drug approval submissions suggest other recently introduced antipsychotic drugs are not P-gp substrates, ie, asenapine, brexpiprazole, pimavanserin, iloperidone, and cariprazine.

In medical decision-making, NMAs are commonly used in health technology assessments produced by government agencies or pharmaceutical companies in connection with technology approval submissions [ 8- 10].

In December 2001, VCEG and MPEG (Moving Picture Experts Group) formed a JVT to finalize the draft of new coding standard for formal approval submission as H.264/AVC [5] in March 2003.

Requirements on dissertation format and the timeline for dissertation format checks, approval, submission and post-defense deposit, per the Graduate School policy.

Following approval from the GUHREC, a further ethics approval submission was made to the Far North Queensland Human Research Ethics Committee FNQHRECC).

In the recent FDA-accelerated approval submission, FISH is also the molecular test that was filed as a companion diagnostic.

A structure such as that described by MIAME/MINTox (MGED Society 2004) would be useful for review of genomics data within the context of a drug approval submission.

The principles may usefully feed in to their app store approval policies (posing more of a question for Google on that front, since it doesn't operate the same kind of pre-approval submissions policy for the Google Play store).

It applies to new drug substance and drug product during clinical development and subsequent applications for marketing, as well as specific cases of post-approval submissions of marketed products and to new marketing applications.

While much of this information is not contained in any "official guidance document" it should nevertheless be a useful template for development of the original submission Pharmaceutics Development Report and aid in developing and justifying post approval change submissions as well.