Back to Results
First PageMeta Content
Technology / Pharmaceutical industry / Clinical research / Food law / Pharmaceuticals policy / Premarket approval / Medical device / Federal Food /  Drug /  and Cosmetic Act / Validation / Food and Drug Administration / Medicine / Health


Federal Register / Vol. 80, NoWednesday, May 6, Notices Submit electronic comments on the draft guidance to http:// www.regulations.gov. Submit written comments to the Division of Dockets Management (HFA–
Add to Reading List

Document Date: 2015-05-06 10:38:11


Open Document

File Size: 214,20 KB

Share Result on Facebook

City

Rockville / /

Company

Accredited Laboratories / Magnetic Resonance Imaging Systems / /

Currency

pence / /

/

Facility

Laboratory Packages By Accredited Laboratories / /

IndustryTerm

supplemental applications / pediatric devices / drug products / pediatric device / premarket approval applications / /

MedicalCondition

disease / Zoonoses / Pain / Trypanosoma cruzi Infection / Guidance Concerning Recommending Customs’ Seizure / /

MedicalTreatment

CPR / /

Organization

DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration / Congress / Food and Drug Administration / Center for Devices and Radiological Health / Division of Dockets Management / Availability AGENCY / Radiological Health / office of Management and Budget / Center for Drug Evaluation and Research / Center for Devices / /

Person

Silver Spring / Draft Guidance / Leslie Kux / /

/

Position

Governor / Director / statistical model for extrapolation / Commissioner / Surgeon / General / Associate Commissioner for Policy / /

ProvinceOrState

Maryland / /

Technology

Gene Therapy / Antibodies / Comparability Protocols / http / /

URL

www.regulations.gov / http /

SocialTag