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Title OpDiv/StaffDiv Guidance Status Sort ascending Issue Date
Comparability Protocols for Human Drugs and Biologics: Chemistry, Manufacturing, and Controls Information Guidance for Industry  Food and Drug Administration (FDA) Proposed
Comparative Analyses and Related Comparative Use Human Factors Studies for a Drug-Device Combination Product Submitted in an ANDA: Draft Guidance for Industry  Food and Drug Administration (FDA) Proposed
Contact Dermatitis From Topical Drug Products for Cutaneous Application: Human Safety Assessment Guidance for Industry  Food and Drug Administration (FDA) Proposed
Contents of a Complete Submission for Threshold Analyses and Human Factors Submissions to Drug and Biologic Applications  Food and Drug Administration (FDA) Proposed
Coronary Drug-Eluting Stents — Nonclinical and Clinical Studies -Companion Document  Food and Drug Administration (FDA) Proposed
Coronary Drug-Eluting Stents-Nonclinical and Clinical Studies  Food and Drug Administration (FDA) Proposed
CPG Sec 527.300 (Draft) Dairy Products - Microbial Contaminants and Alkaline Phosphatase Activity  Food and Drug Administration (FDA) Proposed
CPG Sec 540.750 Draft Revision - Use of The Seafood List to Determine Acceptable Seafood Names  Food and Drug Administration (FDA) Proposed
CPG Sec 550.050 (Draft) Canned Ackee, Frozen Ackee, and Other Ackee Products – Hypoglycin A Toxin  Food and Drug Administration (FDA) Proposed
CPG Sec 575.100 Draft Revision - Pesticide Chemical Residues in Food - Enforcement Criteria  Food and Drug Administration (FDA) Proposed
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