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Cardiology

Bioequivalence Study

With more than 100+ studies conducted, Biometrik Riset Indonesia has built a brand of excellence in conducting Bioequivalence (BE) studies to support generic drugs.

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Gastroenterology

Clinical Research

Clinical trials are research studies intended to answer scientific questions and find better ways to treat or prevent diseases

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Biometrik Riset Indonesia Commitment to Bioequivalence Study

Effi Setiawati - Operation Director

Bioequivalence study is very beneficial in the pharmaceutical industry and the wider community in general, therefore Biometrik Riset Indonesia is always committed to being a reliable and affordable laboratory with high validity of test results and quality according to national and international regulations.


More About Biometrik Riset Indonesia

The Reasons Why You Choose to Use Biometrik Services

We are a Contract Research Organization in Bioequivalence Studies and Clinical Trial.


  • Bioanalytical Lab Services At Industry Leading Turnaround
  • Tailor-Made, High-Value Bioanalysis Services For Biotech
  • Preclinical/Clinical Bioanalysis On Your Drugs
  • Bioanalytical Solutions For Small And Large Molecules
  • The validity of the results can be justified
  • Free Preliminary Consulting with our expert team
  • Effective project management
  • In-Depth understanding of Local Regulatory (BPOM and Ethics Committee)

Testimonials

What Our Client Say

Our Happy Customers

With adequate clinical and laboratory facilities, Bioequivalence testing is carried out in accordance with applicable guidelines with a relatively fast timeline. Breaking code product is done comprehensively and clearly. Bioequivalence test report provided on time.

Bintang Agustri GultomRegulatory Affairs Manager - PT Amarox Pharma Global

The process of implementing the Bioequivalence study in Biometrics runs according to a mutually agreed timeline. During the development and preparation process of the Bioequivalence study Product, Biometrics can be a good discussion partner in providing input regarding the critical parameters of the Test Product that can affect the success of the Bioequivalence Study.  

Harbani IndriartoRnD Manager - PT Promed Rahardjo

Publication

Recent Articles and News

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PT Biometrik Riset Indonesia Reinforces Commitment to National Standards Through BPOM Audit

Writer: dr. Ria Oktavia cc.jpg

Depok, November 24th 2025 – The Bioavailability and Bioequivalence (BA/BE) Center of PT Biometrik Riset Indonesia welcomed an audit by the Indonesian Food and Drug Authority (BPOM) as part of the regulatory assessment to ensure compliance with national standards for BA/BE study implementation.

The audit team from BPOM carried out a comprehensive review of the facilities, including laboratory operations, documentation systems, drug storage conditions, temperature monitoring, operational SOPs, and the conduct of both clinical and bioanalytical phases of the studies.

The ...

PT Biometrik Riset Indonesia Wins Ministry of Health Tender for Bioequivalence Testing Services in 2025

PT Biometrik Riset Indonesia Wins Ministry of Health Tender for Bioequivalence Testing Services in 2025

Writer: Pandu Saputra; Editor: Rizky Puspita Dewi

WhatsApp Image 2025-10-23 at 15.54.30_4a4f7926.jpg

Jakarta, August 22, 2025 – PT Biometrik Riset Indonesia is proud to announce its success in winning the tender from the Ministry of Health of the Republic of Indonesia (Kemenkes RI) for providing bioequivalence (BE) testing services and facilitation of the change from imported to domestic raw materials for the drugs sitagliptin, imatinib, and rivaroxaban for the 2025 fiscal year.

This renewed trust from the Ministry of Health reinforces PT ...

Sponsor Audit: Biometrik’s Commitment to Quality and Compliance

Writer : Andi Darmawan

On September 10, 2025, PT Biometrik welcomed a sponsor audit at its laboratory facilities. One of the sponsors conducting the audit was PT Tropica Mas Pharmaceuticals, as part of their evaluation to ensure that the laboratory meets all regulatory requirements and international standards before being entrusted with conducting bioequivalence studies.

The audit was carried out over a full day and covered a wide range of critical aspects, including:

  • Quality Management System, reviewing standard operating procedures (SOPs), documentation, and quality control workflows implem...


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