Key Capabilities

An integrated team covering standardization, preclinical, clinical, and regulatory workstreams for natural product development in Indonesia.

Raw Material Standardization

Botanical authentication and extract characterization.

Preclinical Testing

Toxicity, pharmacodynamic, and safety pharmacology studies.

Clinical Trial Execution

Clinical studies for natural products, standardized herbal medicines, and health supplements, run at qualified Indonesian sites.

Analytical Laboratory

Marker compound assay and stability testing support.

Medical Writing

Protocols, study reports, and registration dossiers.

Regulatory Affairs

BPOM registration pathways for traditional herbal medicine, standardized herbal medicine, and phytopharmaceuticals.

Biostatistics

Statistical analysis plans, sample size, and reporting.

Post-Market Surveillance

Real-world safety monitoring after registration.

Ready to discuss your Natural Products program?

Our integrated team is ready to design a study tailored to your development goals.