The phrase "armed registry" is correct and usable in written English.
It can be used in contexts related to firearms, security, or law enforcement, typically referring to a database or list of registered firearms or individuals authorized to carry weapons.
Example: "The government has implemented a new armed registry to keep track of all registered gun owners in the country."
Alternatives: "firearm registry" or "weapons registry".
"It's the largest recorded transfer in the U.N. arms registry database in five years, at least.
The OUCH-PRO Study is a prospective multicenter single-arm registry design to study clinical and angiographic outcomes after everolimus-eluting stent (EES).
A prospective multicenter single-arm registry in 49 patients with witnessed cardiac arrest who were selected for MHyT.
This study is a multicentre prospective single-arm registry study and the protocol is approved by the ethics committee at the coordinating centre and by the local institutional review board at each participating centre.
On the heels of the Magnotta case, Shane and Sia, along with Nevada state senator Mark Menudo, are now working again with AWI's Chris Heyde who, armed with expert psychological testimony, is introducing an animal abuser registry bill.
Republicans armed themselves with disputed talking points from the gun lobby about how a bill to expand background checks and outlaw a national gun registry was instead tantamount to a national gun registry.
In response, Mr. Taylor built up his arsenal, paying arms dealers with registry revenues or smuggled diamonds from Sierra Leone, where Mr. Taylor is under indictment in war crimes.
From a total of 194 enrolled patients, 140 subjects were randomized to PCI with or without embolic protection, and 54 were included in a registry arm due to the presence of angiographic exclusion criteria.
Patients with any disease duration were enrolled in CLEAR II, a cross-sectional arm of the registry, beginning in 2006.
Successful approaches for integrating PROs into device evaluation trials include the careful selection of appropriate, interpretable PRO end points, accounting for possible confounding factors, and the use of alternatives to placebo-controlled trial designs, such as single-arm pre post, observational, and registry studies, when the use of placebo control groups is not feasible.
Patients in the Australian arm of the SITS registry were treated according to standard eligibility criteria according to national guidelines (Wright et al., 2012).
