Trusted Clinical Research and Bioanalysis Partner for Pharmaceutical Quality

"Quality Data for Confident Regulatory Decisions"

Pro Q Bioscience is a trusted testing laboratory and Contract Research Organization (CRO) providing high-quality services in Bioavailability/Bioequivalence (BA/BE) studies, clinical trials, and bioanalytical testing. Our work is conducted in compliance with the latest SNI ISO/IEC 17025 standards and Good Clinical Practice (GCP), ensuring reliable data to support pharmaceutical quality and regulatory requirements

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Our Vision

Dedicated to establishing itself as a trusted testing laboratory and Contract Research Organization (CRO), equipped with strong capabilities, professional expertise, and a high level of responsibility to meet client needs in accordance with both local and international standards

Our Mission

Committed to continuously developing the organization and implementing the SNI ISO/IEC 17025:2017 management system and Good Clinical Practice (GCP) with continues improvement in effectiveness and consistent application.
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Our values

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Independency

Professionalism

Confidentiality and Integrity

Efficient

Expertise and Commitment to the quality and ethical conduct

Care, responsive, and reliable

Our Main Service

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Bioavailability & Bioequivalence (BA/BE) Studies

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Clinical Trial Services

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Bioanalytical Testing

pathologycam testing

Pharmaceutical Quality Testing

mineral assay

Research & Development Support

parmaceutical reserach

Bioanalytical Testing

Why Choose Us

Scientific Excellence

We deliver accurate, reliable, and internationally acceptable data supported by competent experts and validated methods

Regulatory Compliance

Our operations comply with recognized standards, including SNI ISO/IEC 17025 and Good Clinical Practice (GCP)

Quality Commitment

A robust quality management system ensures consistency, traceability, and continuous improvement in all activities

Client-Focused Approach

We build long-term partnerships by understanding client needs and providing responsive, professional support

Advanced Capability

Modern analytical technology and experienced teams enable us to handle complex research and testing requirements

Regulatory Confidence

We understand national regulatory expectations and provide data packages suitable for submission requirements

Efficient Study Management

Timelines and project coordination are optimized to support product registration targets

Local Expertise

Strong understanding of the Indonesian pharmaceutical industry environment

Integrated Services

From study planning to final report — all in one place

Our Team

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Mamat Rachmat

Head of Laboratory Department
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Asra Rahama Adiarty Putra

Technical Manager

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Agnesya Elysabeth Kodisu

Responsible in Quality Management

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Chesilia Pangestu

Administration and Scientific Data Analyst

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Harris Jefferson Susanto

Bioanalytical Supervisor

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Millatul Karimah

Laboratory Analyst

Our Facilities