General Affairs Committee
The committee deals with JGA's organizational management , public relations, and financial issues.
Regulatory Affairs Committee
The committee deals with regulatory issues related to the approval and license of generic medicines.
Reevaluation Committee
The committee deals with regulatory issues related to reevaluation of approved medicines stipulated by the relevant law.
Pharmaceutical Technology Committee
The committee is for exchanging information and knowledge on the development of pharmaceutical science, formulation technology and regulatory guidelines.
Drug Safety Committee
The committee deals with safety issues such as safety information, GVP(Good Vigilance Practice) and GPSP(Good Post-Marketing Study Practice).
Quality Committee
The committee deals with quality assurance issues such as GQP(Good Quality Practice) and GMP(Good Manufacturing Practice).
Customer Consultation Committee
The committee is for exchanging opinions on appropriate way and skill of information provision for medical professionals and patients.
Intellectual Property Committee
The objectives of the committee include to safeguard common interests of member companies on national and international pharmaceutical IP matters and to help promote the competitiveness of the generic industry.
Distribution Improvement Committee
The committee deals with distribution issues such as further promotion of transparency in distribution and stable supply of generic medicines.
NHI Pricing Committee
The committee deals with NHI(National Health Insurance) related matters such as drug pricing and reimbursement system, medical service fees and dispensing fees.
International Affairs Committee
The committee is for exchanging and reviewing information on global generic medicine issues related to market trend, regulatory affairs, intellectual property and other business topics. The committee also promotes global collaboration with oversea generics industry associations.
Environment Committee
The committee reviews and promotes environmental conservation activities by gathering information about trends of countermeasures against global warming and reduction of industrial wastes in cooperation with other pharmaceutical associations.
Code of Practice Committee
The committee aims to ensure each JGA member's compliance with Code of Practice and Fair Competition Code.
Ethics Committee
The Committee aims to ensure each JGA member company compliant with corporate ethic code, as well as the JGA Charter of Corporate Behavior and Compliance Program Guidelines.
Biosimilar medicines Committee
The area of focus included to collect and discuss information related to biosimilar medicines both from local and global sources, and provide relevant information to multiple stakeholders.
Public Affairs Committee
The committee aims to plan and manage following activities with respect to external public relations of each committee, publication of JGA news, place advertisement, participation in events such as academic conferences, and websites.
Task Force for Further Promotion of Generic Medicine Use
The task force is responsible for review on actions to be taken by industry side in response to the "Roadmap for Further Promotion of Generic Medicine Use"announced by the Ministry of Health,Labour and Welfare in April,2013.
Policy Committee
This committee formulates the views of the association on the future vision of the generic pharmaceutical industry as well as on the relevant important issues.