South Korea eases requirements for drug imports | Healthcare Asia Magazine
, Korea

South Korea eases requirements for drug imports

Pharmaceutical companies could benefit from the government’s drive to reduce regulatory uncertainty.

The Ministry of Food and Drug Safety of South Korea has minimised the steps required for the import of new biologic agents such as COVID-19 vaccines, by waiving the need for foreign drug developers looking to export their products to the country to present certificates from their respective country.

According to a report from Fitch Solutions, this would speed up the approval process for foreign-developed biologic agents that are urgently needed to counter public health emergencies or that could help patients with rare diseases.

“The government's drive to reduce regulatory uncertainty and improve investor sentiment will yield benefits for the pharmaceuticals sector,” the report stated.

The ministry has also introduced a legal basis to allow drug developers to skip phase III clinical trials for orphan drugs used to treat a rare disease or condition, when there is a limited number of patients who can join their phase III clinical study in the country.

Instead of phase III results, the ministry would ask orphan drug developers to hand in relevant phase II clinical study results. The government expects the revision could incentivize orphan drug developers and provide more options to local patients with rare diseases who suffer from a shortage of treatment choices.

Korea is fast becoming a major player in the pharmaceutical industry, especially within the biotech arena, Fitch noted, as the ongoing business transformation among South Korean companies towards drug discovery will see the introduction of more innovative treatments.

With over 900 new medicines under development, Korean pharmaceutical companies now boast ownership of 4% of global drug development pipelines. As of 2017, Korea developed 29 new medicines and of the new medicines, a total of eight new drugs were approved by the US FDA and nine new drugs were approved by EMA, as of March 2018.

“Mirroring the trajectory of their Japanese peers, South Korean firms have made significant investments in R&D as they seek to shift away from their traditional focus on generic drugs. Spurred on by government incentives such as subsidies and tax breaks, the ratio of R&D spending to sales has increased among South Korean drugmakers,” the report stated.

Join Healthcare Asia Magazine community
Since you're here...

...there are many ways you can work with us to advertise your company and connect to your customers. Our team can help you dight and create an advertising campaign, in print and digital, on this website and in print magazine.

We can also organize a real life or digital event for you and find thought leader speakers as well as industry leaders, who could be your potential partners, to join the event. We also run some awards programmes which give you an opportunity to be recognized for your achievements during the year and you can join this as a participant or a sponsor.

Let us help you drive your business forward with a good partnership!