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2025-10-27 13:40
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Policy
Series of expectorant Prospan generics enter KOR mkt
by
Lee, Tak-Sun
Dec 22, 2023 05:46am
Generic versions of Prospan Syrup, a drug that dominated the phyto-expectorant market in the 2000s, are again being introduced to the market. Prospan Syrup, which has been resold by Kwangdong Pharmaceutical since 2012, is the only available 200mL bottle formulation of Prospan, and 7.5mL and bottle formulations of the drug are only availa
Policy
Delayed re-evaluation of hyaluronic acid eye drops
by
Lee, Tak-Sun
Dec 21, 2023 05:54am
The re-evaluation of the reimbursement appropriateness of hyaluronic acid (HA) eye drops has ultimately been delayed. On the 7th, the Health Insurance Review and Assessment Service (HIRA)¡¯s Drug Reimbursement Committee decided to conduct an additional review of the re-evaluation item. Similarly, on the 20th, the Ministry of Health and W
Policy
Braftovi Cap. & Bosulif tablets reimb for the New Year
by
Lee, Tak-Sun
Dec 21, 2023 05:39am
Starting on Jan 1 next month, two anti-cancer drugs will be reimbursed. These drugs include Ono Pharmaceutical Korea¡¯s Braftovi Cap. 75mg (encorafenib) and the 3 Pfizer Korea¡¯s Bosulif tablet tiems. Braftovi has been listed following drug price negotiation with the National Health Insurance Service, and Bosulif was not subject to maximum
Company
30 companies do not fulfill disability employment obligation
by
Kim, Jin-Gu
Dec 21, 2023 05:39am
Twenty-nine Korean pharmaceutical and biotech companies have failed to fulfill their obligations to hire people with disabilities. The Ministry of Employment and Labor added AstraZeneca Korea to the list for 10 consecutive years and Kolon Pharmaceutical for 3 consecutive years due to their failure in fulfilling their disability hiring obli
Company
¡®Use of Cosentyx will rise in ankylosing spondylitis¡¯
by
Son, Hyung-Min
Dec 21, 2023 05:39am
Reimbursement for Novartis' Cosentyx has been expanded to the first-line in ankylosing spondylitis in Korea. The rise of the new reimbursed drug option in the treatment of early ankylosing spondylitis, which is added to the existing options of tumor necrosis factor-alpha (TNF-¥á) inhibitors such as Humira and Remicade, is expected to increas
Company
One-shot Luxterna may soon receive reimbursement
by
Eo, Yun-Ho
Dec 21, 2023 05:39am
The one-shot retinal disease treatment 'Luxterna' is likely to be reimbursed soon. According to industry sources, Novartis Korea completed negotiations for Luxturna (voretigene neparvovec), a treatment for inherited retinal dystrophy (IRD), with the National Health Insurance Service on the 18th. Although the drug pricing negotiations d
Opinion
[Reporter¡¯s view] Dilemma of compassionate use
by
Son, Hyung-Min
Dec 20, 2023 05:41am
Recently, certain global pharmaceutical companies have decided to discontinue compassionate use of its drugs, which permits patients access to investigational drugs, following the official approval of these drugs in Korea.. Consequently, patients without alternative treatment options are left with no choice but to obtain the drugs at a no
Company
Marketability of homegrown drugs being tested in the US
by
Chon, Seung-Hyun
Dec 20, 2023 05:41am
Domestic pharmaceutical and bio companies are entering the US one after another. GC Biopharma succeeded in entering the US market with its blood product on its third try. Since last year, 3 domestically developed drugs have passed the US market gateway, starting with Hanmi Pharmaceutical and Celltrion. Until now, homegrown drugs that have entere
Policy
Bill pending on substituting dispositions for illegal rebate
by
Lee, Jeong-Hwan
Dec 20, 2023 05:40am
A bill that would allow companies to substitute the price cut/rebate suspension dispositions made on their respective drugs due to rebates has been put on hold at the Standing Committee¡¯s Legislation and Judiciary Subcommittee stage. The review for the bill continued after the Ministry of Health and Welfare, the ministry in charge of the
Opinion
[Reporter's view] Bothered by the PE exemption system
by
Eo, Yun-Ho
Dec 20, 2023 05:40am
The pharmacoeconomic evaluation exemption system is receiving much scrutiny. Under the pretense of improving the system, there are growing voices in favor of reducing of the system, supporting its reduced and limited application. These discussions reached culmination in a session titled, ¡®On improving the pharmacoeconomic evaluation exem
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