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Regulatory updates. Practical perspectives.
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When you designing your home use device : FDA Guidance

When you designing your home use device : FDA Guidance

When you designing your home use device : FDA Guidance

Jun 13 2022 When developing a new home use device, you should take the considerations in this FDA guidance into account and, to the...

FDA Regulations

Provision Consulting Group

Jun 13, 20224 min read

Dermal Fillers, Aesthetic Medical Devices Regulated by FDA

Dermal Fillers, Aesthetic Medical Devices Regulated by FDA

Dermal Fillers, Aesthetic Medical Devices Regulated by FDA

Jun 10 2022 Aesthetic (cosmetic) devices are typically used to improve appearance. They may be regulated by FDA depending upon their...

FDA Regulations

Provision Consulting Group

Jun 10, 20224 min read

FDA Regulation of Product Label with Expiration Dates

FDA Regulation of Product Label with Expiration Dates

FDA Regulation of Product Label with Expiration Dates

Jun 06, 2022 The United States Food and Drug Administration develops and administers regulations under authority granted by laws passed...

FDA Regulations

Provision Consulting Group

Jun 6, 20223 min read

Quality System FDA Regulation for Medical Devices

Quality System FDA Regulation for Medical Devices

Quality System FDA Regulation for Medical Devices

Jun 03 2022 Manufacturers must establish and follow quality systems to help ensure that their products consistently meet applicable...

FDA Regulations

Provision Consulting Group

Jun 3, 20224 min read

FDA Warning Letter to Zhejiang Gaorong Cosmetic: Why Quality Control Matters for Cosmetic and OTC Manufacturers

FDA Warning Letter to Zhejiang Gaorong Cosmetic: Why Quality Control Matters for Cosmetic and OTC Manufacturers

FDA Warning Letter to Zhejiang Gaorong Cosmetic: Why Quality Control Matters for Cosmetic and OTC Manufacturers

20 hours ago

Your Device Is FDA-Cleared. Who Is Your U.S. Initial Importer?

Your Device Is FDA-Cleared. Who Is Your U.S. Initial Importer?

Your Device Is FDA-Cleared. Who Is Your U.S. Initial Importer?

Nov 6

FDA Finalizes Mandatory Cosmetics Recall Guidance: What K-Beauty Brands Entering the U.S. Should Know

FDA Finalizes Mandatory Cosmetics Recall Guidance: What K-Beauty Brands Entering the U.S. Should Know

FDA Finalizes Mandatory Cosmetics Recall Guidance: What K-Beauty Brands Entering the U.S. Should Know

Oct 30

Renew Your FDA Initial Importer Designation with Provision

Renew Your FDA Initial Importer Designation with Provision

Renew Your FDA Initial Importer Designation with Provision

Oct 16

OTC Drug Establishment Renewal: Time to Renew with Provision

OTC Drug Establishment Renewal: Time to Renew with Provision

OTC Drug Establishment Renewal: Time to Renew with Provision

Oct 16

FDA Food Facility Registration: 2026 Is a Renewal Year

FDA Food Facility Registration: 2026 Is a Renewal Year

FDA Food Facility Registration: 2026 Is a Renewal Year

Oct 14

FY2027 FDA Medical Device Registration Renewal: It’s Time to Renew with Provision

FY2027 FDA Medical Device Registration Renewal: It’s Time to Renew with Provision

FY2027 FDA Medical Device Registration Renewal: It’s Time to Renew with Provision

Oct 14

FDA’s FY2027 Medical Device Guidance Agenda: What Could It Mean for 510(k) Manufacturers?

FDA’s FY2027 Medical Device Guidance Agenda: What Could It Mean for 510(k) Manufacturers?

FDA’s FY2027 Medical Device Guidance Agenda: What Could It Mean for 510(k) Manufacturers?

Oct 7

Provision CEO Sung Kwon to Speak at Cosmoprof Asia Hong Kong 2026

Provision CEO Sung Kwon to Speak at Cosmoprof Asia Hong Kong 2026

Provision CEO Sung Kwon to Speak at Cosmoprof Asia Hong Kong 2026

Oct 2

FDA’s Purolea Warning Letter: What AI-Assisted GMP Documentation Means for Manufacturers

FDA’s Purolea Warning Letter: What AI-Assisted GMP Documentation Means for Manufacturers

FDA’s Purolea Warning Letter: What AI-Assisted GMP Documentation Means for Manufacturers

Sep 23

FDA Form 483 Response Is Not the Finish Line: What the Bausch & Lomb Warning Letter Reveals About CAPA

FDA Form 483 Response Is Not the Finish Line: What the Bausch & Lomb Warning Letter Reveals About CAPA

FDA Form 483 Response Is Not the Finish Line: What the Bausch & Lomb Warning Letter Reveals About CAPA

Sep 19

FDA Sunscreen Regulatory Update: PABA and Trolamine Salicylate Removed from OTC Monograph M020

FDA Sunscreen Regulatory Update: PABA and Trolamine Salicylate Removed from OTC Monograph M020

FDA Sunscreen Regulatory Update: PABA and Trolamine Salicylate Removed from OTC Monograph M020

Sep 16

What Does It Mean When Torriden Delegates U.S. Regulatory Compliance to Provision Consulting Group?

What Does It Mean When Torriden Delegates U.S. Regulatory Compliance to Provision Consulting Group?

What Does It Mean When Torriden Delegates U.S. Regulatory Compliance to Provision Consulting Group?

Sep 9

Introducing the Provision Client Portal (Beta): A New Way to Work With Us

Introducing the Provision Client Portal (Beta): A New Way to Work With Us

Introducing the Provision Client Portal (Beta): A New Way to Work With Us

Sep 9

Why Provision Built R.I.S.E. Turning 50,000+ Real Regulatory Cases into Regulatory Intelligence

Why Provision Built R.I.S.E. Turning 50,000+ Real Regulatory Cases into Regulatory Intelligence

Why Provision Built R.I.S.E. Turning 50,000+ Real Regulatory Cases into Regulatory Intelligence

Aug 28

FY2027 FDA Medical Device User Fees Finalized: MDUFA V’s Final Year and What You Need to Know

FY2027 FDA Medical Device User Fees Finalized: MDUFA V’s Final Year and What You Need to Know

FY2027 FDA Medical Device User Fees Finalized: MDUFA V’s Final Year and What You Need to Know

Aug 24

Provision Consulting Group Speaks at ACI Conference on K-Beauty and U.S. Regulatory Challenges

Provision Consulting Group Speaks at ACI Conference on K-Beauty and U.S. Regulatory Challenges

Provision Consulting Group Speaks at ACI Conference on K-Beauty and U.S. Regulatory Challenges

Aug 18

MDUFA VI: Why FDA Device Reviews Are Getting Tougher, Not Faster

MDUFA VI: Why FDA Device Reviews Are Getting Tougher, Not Faster

MDUFA VI: Why FDA Device Reviews Are Getting Tougher, Not Faster

Aug 14

Trapped in Customs: The Hidden Triggers Behind FDA Import Alerts for Medical Devices

Trapped in Customs: The Hidden Triggers Behind FDA Import Alerts for Medical Devices

Trapped in Customs: The Hidden Triggers Behind FDA Import Alerts for Medical Devices

Aug 3

Container Stuck at a U.S. Port — What Triggers an FDA Import Alert for Food and Supplements

Container Stuck at a U.S. Port — What Triggers an FDA Import Alert for Food and Supplements

Container Stuck at a U.S. Port — What Triggers an FDA Import Alert for Food and Supplements

Jul 27

FDA US Agent: What Happens When They Go Silent — and You Picked Them on Price

FDA US Agent: What Happens When They Go Silent — and You Picked Them on Price

FDA US Agent: What Happens When They Go Silent — and You Picked Them on Price

Jul 20

What Huons' FDA Warning Letter Reveals About Today's CGMP Enforcement

What Huons' FDA Warning Letter Reveals About Today's CGMP Enforcement

What Huons' FDA Warning Letter Reveals About Today's CGMP Enforcement

Jun 30

FDA 510(k) Clearance: Why a "Complete" eSTAR Doesn’t Guarantee Approval

FDA 510(k) Clearance: Why a "Complete" eSTAR Doesn’t Guarantee Approval

FDA 510(k) Clearance: Why a "Complete" eSTAR Doesn’t Guarantee Approval

Jun 29

FDA Sunscreen Ingredient Update: Bemotrizinol Added to the U.S. OTC Monograph

FDA Sunscreen Ingredient Update: Bemotrizinol Added to the U.S. OTC Monograph

FDA Sunscreen Ingredient Update: Bemotrizinol Added to the U.S. OTC Monograph

Jun 23

A Kimchi Brand Just Got Recalled. The Culprit? Anchovies.

Jun 15

KOTRA x Provision Consulting Group to Support Korean Companies at BIO International Convention San Diego

KOTRA x Provision Consulting Group to Support Korean Companies at BIO International Convention San Diego

KOTRA x Provision Consulting Group to Support Korean Companies at BIO International Convention San Diego

Jun 11

The FDA is Cracking Down on Sunscreen Factories—Is Yours Truly Ready?

The FDA is Cracking Down on Sunscreen Factories—Is Yours Truly Ready?

The FDA is Cracking Down on Sunscreen Factories—Is Yours Truly Ready?

Jun 1

FDA-Compliant, Yet Still Sued? The Labeling Risks U.S.-Bound Brands Often Miss

FDA-Compliant, Yet Still Sued? The Labeling Risks U.S.-Bound Brands Often Miss

FDA-Compliant, Yet Still Sued? The Labeling Risks U.S.-Bound Brands Often Miss

May 15

Medical Devices Have IDs Too — The FDA UDI Guide for U.S. Market Entry

Medical Devices Have IDs Too — The FDA UDI Guide for U.S. Market Entry

Medical Devices Have IDs Too — The FDA UDI Guide for U.S. Market Entry

May 4

MoCRA Insight: Same Ingredients, Same Formula — Different FDA Interpretations

MoCRA Insight: Same Ingredients, Same Formula — Different FDA Interpretations

MoCRA Insight: Same Ingredients, Same Formula — Different FDA Interpretations

Apr 24

Longevity and In & Out Beauty: What K-Beauty Brands Are Missing in the U.S. Market

Longevity and In & Out Beauty: What K-Beauty Brands Are Missing in the U.S. Market

Longevity and In & Out Beauty: What K-Beauty Brands Are Missing in the U.S. Market

Apr 13

'Magnif's make p:rem', a K-Beauty Brand, Just Landed at Sephora. Here's What Made It Possible.

Mar 31

Why Your K-Clinic Launch Could Trigger an FDA "Drug Claim" — MoCRA Strategies for 2026

Why Your K-Clinic Launch Could Trigger an FDA "Drug Claim" — MoCRA Strategies for 2026

Why Your K-Clinic Launch Could Trigger an FDA "Drug Claim" — MoCRA Strategies for 2026

Mar 24

One Sunscreen Could Land You on FDA's Blacklist — Have You Checked Your OMUFA FY2026 Status?

One Sunscreen Could Land You on FDA's Blacklist — Have You Checked Your OMUFA FY2026 Status?

One Sunscreen Could Land You on FDA's Blacklist — Have You Checked Your OMUFA FY2026 Status?

Mar 13

Two More Digits. A Lot More Work. — FDA's NDC Format Change Explained

Two More Digits. A Lot More Work. — FDA's NDC Format Change Explained

Two More Digits. A Lot More Work. — FDA's NDC Format Change Explained

Mar 6

K-Beauty FDA Compliance: Why 'Marketing' Is No Longer Enough in the U.S. Market

K-Beauty FDA Compliance: Why 'Marketing' Is No Longer Enough in the U.S. Market

K-Beauty FDA Compliance: Why 'Marketing' Is No Longer Enough in the U.S. Market

Feb 24

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