<--- Back to Details
First PageDocument Content
Food and Drug Administration / Pharmaceutical industry / Validity / Laboratory techniques / Cell biology / Premarket approval / Medical device / Validation / Flow cytometry / Medicine / Biology / Science
Food and Drug Administration
Pharmaceutical industry
Validity
Laboratory techniques
Cell biology
Premarket approval
Medical device
Validation
Flow cytometry
Medicine
Biology
Science

Attachment B CDRH Draft Guidance Cover Sheet

Add to Reading List

Source URL: www.fda.gov

Download Document from Source Website

File Size: 271,82 KB

Share Document on Facebook

Similar Documents

Food and Drug Administration / Food safety / Food law / Adulteration / Generally recognized as safe / Federal Food /  Drug /  and Cosmetic Act / Center for Food Safety and Applied Nutrition / Premarket approval / Dietary supplement / Food and drink / Health / Safety

Microsoft PowerPoint - ditto

DocID: 1gc7K - View Document

Food and Drug Administration / Food safety / Food law / Adulteration / Generally recognized as safe / Federal Food /  Drug /  and Cosmetic Act / Center for Food Safety and Applied Nutrition / Premarket approval / Dietary supplement / Food and drink / Health / Safety

Microsoft PowerPoint - ditto

DocID: 1g6Me - View Document

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Federal Register / Vol. 80, NoWednesday, May 6, Notices Submit electronic comments on the draft guidance to http:// www.regulations.gov.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–

DocID: 1aGhA - View Document

Technology / Medical device / Premarket approval / Validation / Direct-to-consumer advertising / Federal Food /  Drug /  and Cosmetic Act / Title 21 CFR Part 11 / Structured Product Labeling / Medicine / Food and Drug Administration / Health

This document is scheduled to be published in the Federal Register onand available online at http://federalregister.gov/a, and on FDsys.govP DEPARTMENT OF HEALTH AND HUMAN SERVICES

DocID: 1akUI - View Document

Pharmacology / Pharmaceutical sciences / Pharmaceutical industry / Clinical pharmacology / United States Public Health Service / Medical device / Expanded access / Premarket approval / Investigational Device Exemption / Medicine / Food and Drug Administration / Health

CLEAN version with no appendices

DocID: 1ahmv - View Document