Clinova RRS Regulatory & Recruitment Services
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    • Regulatory Support
    • Ethics Committee Support
    • BPOM Submission Coordination
    • Patient Recruitment Support
    • Patient Communication Support
    • Clinical Trial Documentation
    • ISF Binder Support
    • Pharmacy Binder Support
    • Quality Control Checks
    • Accountable deliver & AOR/POD Tracking
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About Us

Supporting Clinical Trials with Regulatory, Patient Recruitment, and Site Support Solutions

Our Expertise

Clinova RRS is a dedicated clinical trial support provider with 6 years of experience across Australia and New Zealand, with a current focus on supporting clinical trial services in Indonesia. We understand that the success of any study hinges on the quality of its administrative and logistical foundation. We bridge the gap between complex regulatory requirements and site readiness, turning operational challenges into organized, clinical-grade solutions.

Who We Support

We provide practical, locally focused support for a diverse range of stakeholders across the clinical research sector, including:
  • Sponsors & CROs (Pharmaceutical & Biotechnology)
  • Medical Institutions (Hospitals, Universities, & Healthcare Organizations)
  • Site Teams (Research Sites, Investigators, & Study Teams)

Our Location

Clinova RRS supports clients across Indonesia’s primary research hubs, including Jakarta, Surabaya, Bandung, Medan, Yogyakarta, Semarang, Makassar, Denpasar, and Palembang. While our current focus is deeply rooted in Indonesia, we also bring 6 years of experience across Australia and New Zealand. In the future, we are strategically planning to expand our high-standard support across the wider Asia-Pacific region and internationally.

Our Core Strengths

Our expertise is built on four key pillars designed to streamline your trial operations:
  • Regulatory & Start-Up Mastery (Ethics Committee and BPOM)
  • Integrated Patient Support
  • Comprehensive Site Readiness (ISF/Pharmacy)
  • Quality & Accountable Logistics (AOR/POD tracking)

Our Commitment to Clinical Excellence

Trust is the most important variable in any trial. We are committed to upholding the highest standards in:
Confidentiality
Discreet handling of all sensitive study and patient data.
Accuracy & Compliance
Meticulous attention to detail in every document and checklist.
Reliable Turnaround
Meeting time-sensitive milestones with dependable support.
Patient-Focused Care
Ensuring materials are clear, professional, and empathetic.

Advancing Clinical Research with the Experts

At Clinova RRS, we aim to make clinical trial support more organized, reliable, and accessible. From Jakarta to the wider region, we help your projects move forward with confidence. Contact us on +61 0405 030 206 or email us at info@clinovarrs.com.
Contact
+61 0405 030 206
info@clinovarrs.com
Operational Hours
Monday – Friday 9:00 AM – 5:00 PM (Closed Weekends)
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