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BioWorld - Wednesday, February 11, 2026
Home » Topics » Regulatory » PMDA

PMDA
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Gold chain link engraved with "partnership"

Japan keen to deepen regional partnerships, says PMDA head

Jan. 26, 2022
By Kohei Kanayasu
TOKYO – Japan’s Pharmaceuticals and Medical Device Agency (PMDA) is refocusing its efforts to strengthen ties with Asian counterparts as COVID-19 and market trends show a clear need for faster drug development, approval and accommodation for ailments more common in the region.  
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Chest X-ray analyzed using CXR-AID

Fujifilm, Lunit get nod for collaborative AI-powered chest X-ray analysis system in Japan

Aug. 20, 2021
By Gina Lee
Fujifilm Holdings Corp. has bagged the Japanese Pharmaceuticals and Medical Devices Agency (PMDA)’s approval for CXR-AID, its artificial intelligence (AI) powered chest X-ray analysis system developed in collaboration with Lunit Inc.
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Drug research illustration

Japan’s volatile policy direction continues as challenge, but R&D remains strong

Aug. 3, 2021
By Gina Lee
Rapid changes, a traditionally conservative approach and a chronic lack of regulatory transparency could undo a lot of the progress that Japan has made in the past few years to speed up approvals and all but eliminate a punishing drug lag that, for decades, held back the development of the country’s biopharma sector.
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Drug research illustration

Japan’s volatile policy direction continues as challenge, but R&D remains strong

July 30, 2021
By Gina Lee
Rapid changes, a traditionally conservative approach and a chronic lack of regulatory transparency could undo a lot of the progress that Japan has made in the past few years to speed up approvals and all but eliminate a punishing drug lag that, for decades, held back the development of the country’s biopharma sector.
Read More
Japanese flag

PMDA moves to speed up approvals of innovative devices, improve predictability

June 16, 2021
By Gina Lee
Japan’s Pharmaceuticals and Medical Devices Agency (PMDA) has been stepping up efforts to bring innovative medical devices to market faster and make the regulatory approval process more predictable and further speed up approval processes that have been known for long delays.
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PMDA warns of shock, anaphylaxis with Joyclu

June 1, 2021
By Mari Serebrov
With 10 cases of serious shock and anaphylaxis, including one death, in the month since Seikagaku Corp.’s osteoarthritis drug, Joyclu (diclofenac etalhyaluronate sodium), launched in Japan, the Pharmaceuticals and Medical Devices Agency (PMDA) issued a blue letter to health care professionals and is adding a warning section to the drug’s Japanese label.
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Pills and bottle

After years of effort, Japan slashes drug lag

Dec. 8, 2020
By Alfred Romann
TOKYO – Steadily over a decade and a half, Japan’s drugs and devices regulator has all but eliminated a huge drug lag that put the second largest drug market in the world well behind most others in terms of the time it took for approvals and patient access to innovative drugs.
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Pills and bottle

After years of effort, Japan slashes drug lag

Dec. 7, 2020
By Alfred Romann
TOKYO – Steadily over a decade and a half, Japan’s drugs and devices regulator has all but eliminated a huge drug lag that put the second largest drug market in the world well behind most others in terms of the time it took for approvals and patient access to innovative drugs.
Read More
Japan flag doctor

Japan’s drug repricing plan to hit some top sellers

Feb. 4, 2020
By Jihyun Kim
HONG KONG – Aiming to increase the financial stability of the national health care insurance system, Japan has announced a list of 17 drugs for which prices will be reduced. The country’s Central Social Insurance Medical Council, an advisory group from the Ministry of Health, Labour and Welfare (MHLW), approved the drug repricing system on Jan. 22.
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Japan’s drug repricing plan to hit some top sellers

Feb. 3, 2020
By Jihyun Kim
HONG KONG – Aiming to increase the financial stability of the national health care insurance system, Japan has announced a list of 17 drugs for which prices will be reduced.
Read More
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