Our company provides comprehensive clinical research services for organizations looking to enter the Indonesian market and navigate the regulatory requirements of the Indonesian FDA (Badan Pengawas Obat dan Makanan, BPOM). We specialize in conducting clinical trials that adhere to both local and international standards, ensuring that products meet the necessary safety, efficacy, and quality benchmarks required for approval.Our team has extensive experience in managing all phases of clinical trials, from protocol development and patient recruitment to data management and regulatory submissions. We work closely with clients to design and execute studies that align with their specific objectives and the regulatory landscape in Indonesia. By leveraging our local expertise and robust infrastructure, we help companies successfully conduct clinical research, facilitating a smoother and more efficient path to market entry. This service is crucial for pharmaceutical and biotech companies aiming to expand their presence in Indonesia and ensure compliance with local regulations..