Domestic and foreign health authorities including the Ministry of Food and Drug Safety and Korea Institute of Drug Safety and Risk Management (KIDS), institutions specified under other laws and regulations, and domestic and overseas clinical trial registration sites such as clinicaltrial.gov |
Compliance with related domestic and foreign laws, such as the Pharmaceutical Affairs Act |
Health information related to safety such as issues (excluding identifying information), information of researchers participating in clinical trials (name, hospital name, contact information), etc. |
Period specified under related domestic and foreign laws, such as the Pharmaceutical Affairs Act |
Ministry of Health and Welfare |
Execution of expenditure report processes in relation to the provision of economic benefits, etc. under the Pharmaceutical Affairs Act and Medical Devices Act |
[Health professionals] Name, organization and address, support amount, application date, support items |
Retaine and used until the purpose of collection is achieved |
Korea Pharmaceutical and Bio-Pharma Manufacturers Association (KPBMA) |
Checking compliance with quarterly reporting obligations under the KPBMA’s Fair Competition Code on Transaction of Pharmaceuticals and compliance with lecture/advisory fee standards under the Fair Competition Code |
[Health professionals] Name, affiliation, amount of payment, date of lecture/consultation, location of lecture/consultation, topic of lecture/consultation |
Korea Medical Devices Industry Association (KMDIA) |
Checking compliance with quarterly reporting obligations under the KMDIA’s Fair Competition Code of Medical Device Transactions and compliance with lecture/advisory fee standards under the Fair Competition Code |
[Healthcare workers] Name, affiliated institution and address, amount of payment, date of lecture/consultation, place of lecture/consultation, topic of lecture/consultation |
Domestic and foreign affiliates and partners of Handok |
Management and analysis of safety information such as issues, data processing and result reporting of various studies such as clinical trials, and compliance with domestic and foreign laws |
Health information related to safety such as issues (excluding identifying information), various research subjects’ health information such as for clinical trials collected via subject identification code, name and contact information of the researcher in clinical trials, etc. |
Retained until the date of withdrawal of consent or the purpose for which it was provided |