Vaccine, Immunology, and Infectious Disease

Our end-to-end services are designed to streamline your clinical trial process and mitigate risk:

• Strategic Site Selection
  We identify and qualify the most suitable Principal Investigators (PIs) from our network and high-performing sites, ensuring rapid patient enrollment. Our strong, long-term relationships with these sites enable a rapid start-up and predictable execution for your study. Click here to see our success story.
   

• Regulatory Submissions and Compliance
  Our experts manage all submissions to Ethics Committees (EC) and BPOM, navigating the local regulatory landscape to secure approvals efficiently. We have a strong relationship with BPOM and the Ministry of Health (MoH), and a deep understanding of the unique regulatory requirements for vaccine trials. 
  
  We are proud that our sites have successfully undergone inspections by international authorities such as BPOM, PMDA (Japan), and NMPA (China), a testament to our commitment to global quality standards.
   

• Proactive Clinical Monitoring
  Equilab's experienced Clinical Research Associates (CRAs) conduct rigorous monitoring to maintain data integrity and adherence to regulatory standards from site initiation, interim monitoring, until site closeout.
   

• Pharmacovigilance
  We implement a comprehensive safety monitoring system to manage adverse events swiftly and accurately, protecting patient welfare and your data.
   

• Investigational Product (IP) and Sample Management
  As your Importer of Record (IoR), Equilab simplifies the complex logistics of importing your Investigational Product (IP) into Indonesia. We provide secure depot facilities with strict temperature control for IP storage and distribution. Additionally, our central laboratory offers state-of-the-art biomedical freezers (-20°C and -70°C) for storing and managing your clinical trial samples. This integrated approach ensures the integrity of your IP and samples while reducing your logistical burden.
   

• Project and Site Management
  Our dedicated Clinical Project Managers (CPMs) are specialists in endocrinology research. With over 20 years of collective experience, our team ensures your study adheres to all protocol and quality standards. We maintain transparent communication and close coordination with clinical sites to ensure smooth progress and help you achieve your research goals.
   

• Seamless Data Management and Statistical Analysis
  Our team handles large, complex datasets from thousands of subjects, providing reliable and clean data for analysis. Equilab also involved in many vaccine studies to perform the statistical analysis and deliver the report to the Sponsor.