Cosmetic Product Registration - South Korea

K

kp7788

#1
Hi Everyone,

I am interested in knowing the steps involved in registering a cosmetic product in Korea (for a US-based company).

Also, will it require approval from KFDA or some other organization?

Please do tell your views on this.

Thanks in advance.
 
Elsmar Forum Sponsor

Stijloor

Staff member
Super Moderator
#2
Hi Everyone,

I am interested in knowing the steps involved in registering a cosmetic product in Korea (for a US-based company).

Also, will it require approval from KFDA or some other organization?

Please do tell your views on this.

Thanks in advance.
Can someone help?

Thanks.

Stijloor.
 
Thread starter Similar threads Forum Replies Date
M SOPs for a new Cosmetic Product Development Laboratory Calibration Frequency (Interval) 1
Ajit Basrur Approximately $2 Million of Potentially Harmful "Cosmetic" Eye Product Seized US Food and Drug Administration (FDA) 0
A Regulatory requirements for electrical cosmetic appliances US Food and Drug Administration (FDA) 5
I Writing a Cosmetic Criteria for Switches Document Control Systems, Procedures, Forms and Templates 1
V Placement of cosmetic products on EU market as medical devices EU Medical Device Regulations 2
GoSpeedRacer Validation of Processes 7.5.6 - Do cosmetic welds need process validation? ISO 13485:2016 - Medical Device Quality Management Systems 3
E External Thread Cosmetic/Appearance Inspection, Prints (Drawings), Testing, Sampling and Related Topics 2
E Cosmetic Standard for Sheets of Extruded Plastic Manufacturing and Related Processes 1
P Cosmetic Inspection of Plastic Injection Molded Parts Manufacturing and Related Processes 5
A Stuck at 'Analyse' stage of DMAIC Improvement Cycle on Cosmetic Specification Manufacturing and Related Processes 10
Q Please suggest how to improve Cosmetic Visual Inspections Inspection, Prints (Drawings), Testing, Sampling and Related Topics 10
A Cosmetic Visual Inspection Specification Advantages Manufacturing and Related Processes 7
A Cosmetic Spec - Convincing Management Visual Inspection Standard is Necessary Manufacturing and Related Processes 5
R Regulatory Aspects of Co-Packaging Medical Device and Cosmetic Other Medical Device and Orthopedic Related Topics 6
M Human Factors Testing for CE Marking of a Cosmetic Device CE Marking (Conformité Européene) / CB Scheme 9
S Cosmetic Inspection (scratch, black dot, burr) Standard in Manufacturing Inspection, Prints (Drawings), Testing, Sampling and Related Topics 4
J Do Cosmetic GMPs apply for Fragrance Manufacturer US Food and Drug Administration (FDA) 1
Roberticus Blacklight Cosmetic Inspections of Stainless Steel Parts ISO 13485:2016 - Medical Device Quality Management Systems 5
C Corrective Action and Preventive Action for Operator Error (Cosmetic - Handling) Preventive Action and Continuous Improvement 15
C MSA on Attribute Data - Can use Different Parts with Different Cosmetic Issues? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 3
S Medical Device or Cosmetic Device in Korea? Hand Held Wrinkle Reduction LED Light Other Medical Device Regulations World-Wide 1
S Medical Device or Cosmetic Device in Japan? Hand Held Wrinkle Reduction LED Light Japan Medical Device Regulations 3
V Creating a Cosmetic Inspection Specification for Powder Coated Painted Finished Parts Manufacturing and Related Processes 7
H Business Process for Cosmetic Manufacturer ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
B Sterilize or Disinfect? Research Cosmetic Device Other Medical Device and Orthopedic Related Topics 4
P Plate Glass: Cosmetic Inspection for Scratches Inspection, Prints (Drawings), Testing, Sampling and Related Topics 5
R Eliminating Cosmetic Issues and Customer Complaints Problem Solving, Root Cause Fault and Failure Analysis 14
R Cleaning Validation Protocol in a Cosmetic company ISO 13485:2016 - Medical Device Quality Management Systems 13
M Cosmetic defects on chrome plating - Chrome plating visual standards Manufacturing and Related Processes 6
Ajit Basrur Trending segregated for cosmetic and functional dppm? Automotive requirements Misc. Quality Assurance and Business Systems Related Topics 5
K Cosmetic Specifications - Seeking good example of a cosmetic inspection standard Manufacturing and Related Processes 2
H Medical device Product Registration Registrars and Notified Bodies 2
A Can a power Supply be an accessory to a medical device, if it is an 'off-the-shelf' product. IEC 60601 - Medical Electrical Equipment Safety Standards Series 3
M Extension to shelf life of new product under MDR EU Medical Device Regulations 1
lanley liao Are there guidelines for application of all API monogrammal product? Oil and Gas Industry Standards and Regulations 2
S ISO 11137- Simulated product vs SIP Other Medical Device Related Standards 2
K "World Class Product" based QM. I need advice. Quality Management System (QMS) Manuals 14
R IATF 16949 Certification for new site with transferred product--what is the impact with CSR and scorecards? IATF 16949 - Automotive Quality Systems Standard 0
William55401 Distributed By Product - Best Practices for Configuration Management and Purchasing Controls ISO 13485:2016 - Medical Device Quality Management Systems 0
R Compatibility studies - combination product CE Marking (Conformité Européene) / CB Scheme 4
R Compatibility studies - Medicinal Product and Medical Device Other ISO and International Standards and European Regulations 0
J Marking "Distributed By" to product with distributors' reference-code EU Medical Device Regulations 3
dinaroxentool Selling a product in Both UK and EU after Brexit UK Medical Device Regulations 8
P EU MDR Translation of Product Name EU Medical Device Regulations 0
N Is this a single integral drug device combination product EU MDR CE Marking (Conformité Européene) / CB Scheme 1
V New Product Model CE Mark Certification under MDR EU Medical Device Regulations 0
Sidney Vianna Informational APQP4Wind - Advanced Product Quality Planning for the Wind Power Supply Chain APQP and PPAP 3
K 510k FDA review, will they accept Biocompatibility result generated using feasibility product lots? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 8
G Adopting old product - compliance with IEC 62304 IEC 62304 - Medical Device Software Life Cycle Processes 9
S How long does it take to register a product with MHRA? UK Medical Device Regulations 3

Similar threads

Top Bottom