Sentence examples for ep standards from inspiring English sources

Exact(1)

The primary endpoints were the differences between latanoprost and travoprost ophthalmic solutions in their alignment with the EP-A criteria A, the time to "no recovery" (report of <10 CFU or <1.0 log) for each organism/product combination and the recovered organism counts at 6 and 24 hours as defined in EP standards.

Similar(59)

EP, standard i.m.

IP and EP standard T-scores (normalized on the distribution in the control group, with 50 indicating average and every 10 points representing one standard deviation) were compared in the gifted group using Student's t-test.

Mean IP and EP standard T-scores in the gifted group did not significantly differ (59.8 ± 13.8   versus  61.2 ± 14.6, resp .. Mean CBCL raw scores and subscores across "low gifted" children and "highly gifted" children are listed in Table 3. Mean SC subscore was significantly higher in low gifted children (3.0 ± 2.8   versus 1.7 ± 1.7; P < 0.05); other comparisons showed no significant difference.

The antimicrobial effectiveness testing was conducted at Lancaster Laboratories (Lancaster, Pennsylvania, USA), an independent laboratory, according to the EP-A standards (EP-A; Tables 1 and 2[ 11]).

We also considered that the phoneme conversion corresponds to the EP-standard.

Sepabeads EC-EP (standard grade; specified particle size 150-300 μm; pore size 30-40 nm) were kindly provided by Resindion (Milan, Italy).

*By European Pharmacopoeia-A (EP-A) standards, only required for oral products [ 11].

Anthropometry was measured by a single trained observer (EP) using standard methods (Cameron, 2004; Lohman et al., 1988).

For the seven locations without large clusters of high EP, the standard deviations were smaller, thus supporting more spatial homogeneity in the risks.

Each product was tested for antimicrobial effectiveness by European Pharmacopoeia A (EP-A) standards, the most stringent standards of the three major compendia, which specify two early sampling time points (6 and 24 hours) not required by the United States Pharmacopeia or Japanese Pharmacopoeia.

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