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Equilab International and Mayapada Healthcare Group signed Clinical Trial Agreements (CTA) on 4 September for a global phase 3 diabetes study. The trial will take place at Mayapada Hospital Jakarta Selatan and Mayapada Hospital Kuningan. Representatives attending the ceremony included Ronal Simanjuntak, President Director of Equilab International; dr. Dini Handayani, Chief Medical Officer of Mayapada Healthcare Group; and dr. Deasy Sugesty, Director of Mayapada Hospital Kuningan. The...
On 5 September 2026, the Indonesian Association for the Study of Medicinals (IASMED) convened its annual meeting to evaluate regulatory developments and strategic priorities for clinical research in Indonesia. The event brought together senior government officials and industry representatives, including the Chairperson of the Indonesian Food and Drug Authority (BPOM) – Prof. dr. Taruna Ikrar, M.Biomed., Ph.D., Director General of Pharmaceuticals and Medical Devices at the Indonesian Ministry...
We are pleased to announce that Equilab International has received recognition from the Ministry of Health (MoH) of Iraq as a research centre for Bioequivalence studies, marking another important milestone in strengthening our international regulatory recognition and global presence in Bioequivalence studies. As a leading Bioequivalence Centre in Indonesia and Southeast Asia, this recognition further reflects Equilab’s commitment to maintaining high standards of quality, scientific integrity,...
On 10 September 2026, the Indonesian Food and Drug Authority (BPOM) received a delegation from the Korea National Enterprise for Clinical Trials (KoNECT), Equilab International, and South Korean pharmaceutical companies. Welcomed by BPOM Chairperson – Prof. dr. Taruna Ikrar, M.Biomed., Ph.D., alongside Deputy I for Drug, Narcotics, Psychotropics, Precursors, and Addictive Substances Control – Dr. William Adi Teja, MD., BMed., MMed., and Director of Drug Registration – Dra. Tri Asti Isnariani,...
JAKARTA - The Head of the National Agency of Drug and Food Control (BPOM), Prof. Dr. Taruna Ikrar, M.Biomed., Ph.D., visited an Indonesian independent laboratory, PT Equilab International. This visit is a step taken by BPOM as part of a collaboration to ensure the quality of drug, cosmetic, and food products in Indonesia. "Indonesia is a large country with a vast number of natural herbal products, approximately 17,000 in total. However, there are currently only around 90 standardized herbal medicines and only 21 phytopharmaceuticals. This presents a great potential for conducting clinical trials in Indonesia and enhancing the status of natural herbal products. Equilab is a trusted laboratory in Southeast Asia that complies with BPOM standards and regulations and has experience in performing clinical trials and product quality testing," said Prof. Taruna. The President Director of PT Equilab International, Mr. Ronal Simanjuntak, stated that Equilab has the capability as an independent laboratory in drugs, cosmetics, and food testing and research. Equilab also highlighted its extensive experience in vaccines, infectious diseases, and probiotic clinical trials. "For 22 years, we have been ensuring quality and testing drug, cosmetic, and food products. Equilab already performed more than 1,500 clinical studies including bioequivalence studies, clinical trials, and dermatology testings. In terms of accreditation, we are the only CRO in Southeast Asia accredited by UK MHRA, Malaysian NPRA, BPOM, ISO 17025, and ISO 15189. Our clinical study reports have been accepted in more than 40 countries, including the UK, Germany, the Netherlands, Spain, Hungary, South Africa, Malaysia, and Singapore," said Mr. Ronal. Furthermore, Equilab International continues to innovate by exploring the utilization of artificial intelligence (AI) for research and clinical testing. "We believe that AI can accelerate innovation and increase efficiency in testing," said the Director of Equilab International, Wimala Widjaja.
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Equilab’s Full Spectrum Clinical Research Solutions
A leading independent Contract Research Organization in Indonesia that provides end-to-end services.



World Class
Contract Research
Organization
World-class contract research organization with numerous accreditations are continuously optimizing areas of expertise to expand global reach.



Globally
Approved Reports
Our Clinical Study Reports (CSR) have been approved by 40+ countries across Asia, Europe, and Africa, including regulatory bodies such as WHO and UK-MHRA.



Leading Community-based Clinical Trials
We have vast clinical site network to ensure fast participant recruitment process in vaccine, hormonal, nutritional, and pediatric studies.



TOP 10
CRO
Listed in the top ten Contract Research Organizations (CRO) in Asia Pacific 2022, as featured in Pharma Tech Outlook magazine.







