Field notes
Regulator-specific notes on translation requirements, review workflows, and submission readiness across Latin America.
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6 min read
How to keep a shared device technical core and localize only linguistic and administrative annexes for parallel filings across a twelve-country Latin American plan.
By Julio G. Martinez-Clark
8 min read
Four conditions a medical device translation file must meet before a Latin American filing: one term list, intact numbers, country labels, and the right certification tier.
By Julio G. Martinez-Clark