What We Do

Our Services
and Commitments

From fast-track approval to commercial execution, ACA Pharma helps innovative medicines and devices reach patients faster through Macau, Hong Kong and Singapore pathways, then expands access into Mainland China and other key markets through compliant, end-to-end commercialization.

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AcaPharma team

Macau and Hong Kong Fast-Track for Early Market Access

ACA Pharma specializes in fast-track registration and commercialization pathways that can enable market access in as little as 30 to 90 days post-submission. For medicines through Macau and medical devices through Hong Kong, this is the fastest compliant path into Mainland China’s pilot zones — giving partners a faster route to market, earlier patient access, and a strategic advantage in Greater China.

Our Process
1 Partnership icon
Partnership
Align goals, terms & scope
2 Registration icon
Registration
30–90 day fast-track pathways
3 Marketing icon
Marketing
Build KOL awareness & reach
4 Distribution icon
Distribution
90+ hospitals -> billions reached
Globe showing China and Asia-Pacific region
90+ hospital network
1.4B+ patient reach

Expanding Access. Extending Reach.

Following registration in Macau or Hong Kong, eligible medicines and devices can access a growing network of hospitals across the Guangdong-Hong Kong-Macau Greater Bay Area, Hainan and a other medical pilot zones in Mainland China. This expanded footprint helps bring treatment to a broad patient population more quickly, while also creating a pathway for patients from across Mainland China to travel to designated hospitals for critical care.

Critical Care Solutions

Pediatric and Clinically Urgent Medications:

  • Following registration in Macau, eligible medicines can gain access to leading hospitals in Beijing, Shanghai, Tianjin, Hainan, and Chongqing, as well as 44 of China’s top pediatric hospitals. Classified as clinically urgent and irreplaceable, these medications benefit from a streamlined approval process, entering leading hospitals without the need for national registration or clinical trials.

Fast-Track National Approval:

  • Leveraging initial real-world data collected after Macau registration, national registration is typically completed within 3-6 months for Pediatric Orphan Drugs and 6-12 months for Clinically Urgent Medicines. This streamlined process ensures timely access to critical treatments for patients in need.

Major Media Coverage:

  • Strategic media outreach and market education can help ensure physicians, patients, and families are aware of available treatment options, supporting timely access for those in urgent need.
MACAU Registration hub 44 Pediatric Hospitals 95% rare disease coverage Shanghai Major hospitals Greater Bay Area 71 hospitals Hainan Medical Pilot Zone Chongqing Central access Tianjin Northern access
90+ hospital
network
1.4B+ patient
reach
3–12 mo national
approval

Asia Market Entry Specialists

On-the-ground execution, broader reach

We support rare-disease programs across therapeutic areas, from early access to multi-country expansion beyond China

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