Approval is only the beginning of access.

See how innovative medicines move from regulatory approval through value assessment and price negotiation to real patient access.

๐Ÿ‡บ๐Ÿ‡ธ๐Ÿ‡ช๐Ÿ‡บ๐Ÿ‡ฏ๐Ÿ‡ต๐Ÿ‡ง๐Ÿ‡ท๐Ÿ‡ฎ๐Ÿ‡ณ๐Ÿ‡ฆ๐Ÿ‡บ
Regulatory
HTA
Price
Access

One medicine. Different access logic.

After approval, different institutions, evidence thresholds and negotiation mechanisms determine when patients actually receive treatment.

๐Ÿ‡จ๐Ÿ‡ณ

China

1
NMPAMarketing authorization
2
NHSAValue and negotiation
3
NRDLNational reimbursement list
4
Patient accessImplementation
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South Korea

1
MFDSApproval
2
HIRABenefit assessment
3
NHISPrice negotiation
4
MOHWFinal listing
RSA
๐Ÿ‡ฆ๐Ÿ‡บ

Australia

1
TGARegistration
2
PBACHTA recommendation
3
PBSPricing and listing
4
Patient accessSubsidized use
Pricing by indication

Special mechanisms often determine the real pathway.

From China's national reimbursement negotiation and Korea's RSA and flexible pricing contracts to Australia's indication-based pricingโ€”the differences need explanation, not just a list.

๐Ÿ‡จ๐Ÿ‡ณChina

National reimbursement negotiation

Clinical value + economic evidence
Payment standard + listing
๐Ÿ‡ฐ๐Ÿ‡ทSouth Korea

RSA

Payer
Shared uncertainty
Outcome feedback
๐Ÿ‡ฐ๐Ÿ‡ทSouth Korea

Flexible price contract

Base price
Use / expenditure signal
Price adjustment
๐Ÿ‡ฆ๐Ÿ‡บAustralia

Pricing by indication

Indication
Value difference
Differentiated price

Start with one market. See the complete pathway.

Explore the real decision relationships between regulation, HTA, pricing, reimbursement and post-listing management.