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RAPS 音标拼音: [r'æps]

V.E.R.A. -- Virtual Entity of Relevant Acronyms (June 2006) (vera)

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单词	字典	翻译
raps	查看　raps　在百度字典中的解释	百度英翻中〔查看〕
raps	查看　raps　在Google字典中的解释	Google英翻中〔查看〕
raps	查看　raps　在Yahoo字典中的解释	Yahoo英翻中〔查看〕

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英文字典中文字典相关资料:

Regulatory Affairs Professionals Society | RAPS
RAPS is the largest global organization of and for those involved with the regulation of healthcare and related products, including medical devices, pharmaceuticals, biologics and nutritional products
Upcoming Events - RAPS
RAPS is the largest global organization of and for those involved with the regulation of healthcare and related products, including medical devices, pharmaceuticals, biologics and nutritional products
RAPS Convergence 2026
Where regulatory professionals come together to make crucial connections, share expert insights, and discover the latest innovations
RAC | RAPS
RAPS is the largest global organization of and for those involved with the regulation of healthcare and related products, including medical devices, pharmaceuticals, biologics and nutritional products
Course Catalog | RAPS
RAPS is the largest global organization of and for those involved with the regulation of healthcare and related products, including medical devices, pharmaceuticals, biologics and nutritional products
Join RAPS
RAPS is the largest global organization of and for those involved with the regulation of healthcare and related products, including medical devices, pharmaceuticals, biologics and nutritional products
RAPS Certification and Certificate Portfolio
RAPS is the largest global organization of and for those involved with the regulation of healthcare and related products, including medical devices, pharmaceuticals, biologics and nutritional products
Search - RAPS
RAPS is the largest global organization of and for those involved with the regulation of healthcare and related products, including medical devices, pharmaceuticals, biologics and nutritional products
Who We Are - RAPS
RAPS is the largest global organization of and for those involved with the regulation of healthcare and related products, including medical devices, pharmaceuticals, biologics and nutritional products
FDA consolidates adverse events reporting systems | RAPS
The US Food and Drug Administration (FDA) announced it is unifying its various adverse reporting systems into a single system called the Adverse Event Monitoring System (AEMS) The agency said the move would modernize adverse event reporting systems and provide more transparency

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