HHS:Food and Drug Administration

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FDA Classification and Special Controls for Vaginitis and Bacterial Vaginosis Diagnostic Devices
$19.99
FDA Requirements for Mutation Detection Tests in Myeloproliferative Neoplasms
$9.99
FDA Regulation: Class II Classification of Menopause Test Systems
$19.99
FDA Compliance Training: Pharmacogenetic Assessment System Device Classification (21 CFR 862.3364)
$19.99
FDA Requirements for Liver Iron Imaging Companion Diagnostics in Deferasirox Therapy
$19.99
FDA Regulation of Orthopedic Manual Surgical Instruments for Non-Fusion Spinous Process Spacer Devices
$19.99
FDA Class II Classification for Laparoscopic Gastrointestinal Sizing Tools
$19.99
FDA Rule: Anti-Phospholipase A2 Receptor Immunological Test System Classification & Compliance
$19.99
FDA Compliance for Cancer Predisposition Risk Assessment Systems (21 CFR 866.6090)
$49.99

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Cut Flowers Import Regulations Update: Removal of Chrysanthemum White Rust Restrictions

Oct 9, 2026

Why This Course is Important
Without this course, you risk falling out of compliance with new federal import regulations, potentially facing shipment refusals, business disruptions, and costly legal penalties due to outdated knowledge of import requirements for cut flowers.

Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Cut Flowers Regulations; Removal of Chrysanthemum White Rust-Related Provisions.

Key regulatory references include:

7 CFR Part 319 – Foreign Quarantine Notices

Course SKU
FR-26-3255-1

FDA Regulation: Focused Ultrasound Systems for Non-Thermal, Mechanical Tissue Ablation

Oct 7, 2026

Why This Course is Important
Without this course, you risk overlooking critical compliance steps, potentially leading to market denial, enforcement actions, and increased legal or financial exposure for your organization.

Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Medical Devices; General and Plastic Surgery Devices; Classification of the Focused Ultrasound System for Non-Thermal, Mechanical Tissue Ablation.

Key regulatory references include:

21 CFR Part 878 – General and Plastic Surgery Devices

Course SKU
FR-26-2252-1

HHS:Food and Drug Administration

FDA Classification and Special Controls for Vaginitis and Bacterial Vaginosis Diagnostic Devices

FDA Requirements for Mutation Detection Tests in Myeloproliferative Neoplasms

FDA Regulation: Class II Classification of Menopause Test Systems

FDA Compliance Training: Pharmacogenetic Assessment System Device Classification (21 CFR 862.3364)

FDA Requirements for Liver Iron Imaging Companion Diagnostics in Deferasirox Therapy

FDA Regulation of Orthopedic Manual Surgical Instruments for Non-Fusion Spinous Process Spacer Devices

FDA Class II Classification for Laparoscopic Gastrointestinal Sizing Tools

FDA Rule: Anti-Phospholipase A2 Receptor Immunological Test System Classification & Compliance

FDA Compliance for Cancer Predisposition Risk Assessment Systems (21 CFR 866.6090)

QUICK LINKS

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Accessibility

LATEST Products

Cut Flowers Import Regulations Update: Removal of Chrysanthemum White Rust Restrictions

FDA Regulation: Focused Ultrasound Systems for Non-Thermal, Mechanical Tissue Ablation