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Who We Are

About Us

We are PT Prodia Diagnostic Line (Proline), a business unit of Prodia Group which engaged in IVD industry. Bearing Prodia name, which is known to accentuate quality with more than 45 years of experience in the world of clinical laboratory in Indonesia, Proline also put quality in its products.

Our Vision

To become a leading IVD manufacturer in Indonesia.

Our Mission

To meet national and regional need of qualified IVD products.

The Spirit of Prodia

1. Customer Satisfaction

We put customers first in everything we do. We speak and act with our customers in mind.

2. Excellence

We strive to be better, smarter and more innovative.

3. Attitude

Act positive and focus on solution. We understand that negativity will only decrease our productivity and effectiveness.

4. Teamwork

We support and value our co-workers, and we enjoy working together as a team to achieve more than we can achieve as individuals.

5. Openness

We are open, honest and fair in what we say and do, and take responsibility for our actions.

6. Quality

We provide quality products and services that provide value to customers.

7. Balance

We are committed to maintaining a work/life balance, as well as a business/learning environment at Proline.

What We Do

Our Expertise

We focus on in vitro diagnostic products suitable for a wide range of laboratory sizes which are known for features such as:

  • User-friendly reagent with optimized stability for an outstanding result in clinical chemistry and immunoturbidimetric test which comes with supporting controls, calibrators/standards, and supplementaries.
  • Robust fully-automated and semi-automated clinical chemistry instrument suitable for small to large laboratory testing.
  • Fast, accurate, and user-friendly rapid diagnostic test for reliable point-of-care testing. 

OEM Manufacturing Service

In the field of IVD development and production, we provide all-in-one product customization service starting from the technical product formulation, brand and packaging design, and up to pre and after-sales training and services.

Get to Know More About Us

Read and save information about our company profile by downloading the following files:

Certificates

ISO 13485 : 2016

Clinical Chemistry Production Certificate

Immunology Production Certificate

GMPMD Certificate

GDPMD Certificate

Milestones

2010

April, 2010

Company Establishment

PT Prodia Diagnostic Line (abbreviated as Proline) was officially established in Cikarang, Indonesia with one of its business scopes as a manufacturer of IVD medical devices.

2011

April, 2011

Partnering With DiaSys

DiaSys as one of the world's leading IVD manufacturers with more than 20 years of experience, is officially partnering with Proline in the production of the reagents. By using the same protocol, the product quality manufactured by Proline is equivalent to the product standard made by DiaSys.

October, 2011

Proline Factory Inauguration in Cikarang

More than a year since the construction began, finally on 15 October 2011, Proline's production site in the Industrial Estate of Jababeka III was finished and ready to be used.

2012

February, 2012

Production Certificate

Every manufacturer of medical devices must have a Production Certificate from the Ministry of Health of the Republic of Indonesia. After preparing the work area and procedures and also passing field checks, Proline finally obtained a Production Certificate from the Ministry of Health of the Republic of Indonesia which is mandatory of every manufacturer of medical devices.

April, 2012

Distributor Permit

Proline successfully obtains an IPAK (Medical Device Distributor Permit) from the Ministry of Health of the Republic of Indonesia. This certificate allowing Proline to distribute medical device products to end users in healthcare facilities all around the nation.

July, 2012

Pilot Production

Armed with a Production Certificate and a verified protocol, Proline has successfully carried out the first production of 4 liters of Triglycerides FS.

2014

November, 2014

ISO 13485:2003 Certificate

ISO 13485 is a quality management system standard for the medical device industry. Proline as a company that prioritizes quality in every product and process, was awarded ISO 13485:2003 certificate. This achievement shows Proline's commitment to be able to provide quality products to customers.

2015

January, 2015

Available on E-Catalog Site

Starting January 2015, Proline products will be available to be purchased via e-catalog, a portal for the procurement of medical devices at government health facilities released by LKPP.

June, 2015

GMPMD Certification by Ministry of Health

As an IVD manufacturer, through an audit process carried out by the Indonesian Ministry of Health, Proline successfully received the GMPMD certificate that reflects Proline's commitment to applying the principles of Good Method of Manufacturing of Medical Devices.

2017

April, 2017

GDPMD Certification by Ministry of Health

Proline successfully received the GDPMD certificate released by the Indonesian Ministry of Health. It reflects Proline's commitment to applying the principles of Good Method of Distribution of Medical Devices.

November, 2017

ISO 13485:2016 Certification

Responding to the publication of the latest version of the ISO 13485 standard, going through the recertification process to get ISO 13485:2016 certificate.

2019

October, 2019

Immunology Production Certificate

As proof of our commitment to meeting product eligibility standards, Proline has successfully obtained a production certificate for immunological products from the Indonesian Ministry of Health.

November, 2019

The Inauguration of INBIO

On November 13, 2019, Proline inaugurated INBIO as its new production line in the scope of immunology. This division focuses on the development and production of products such as lateral flow immunochromatography tests.

2020

November, 2020

ISO 13485:2016 Certification by TUV NORD Indonesia

As a company that prioritizes quality in every product and process, Proline's quality management system successfully complies with ISO 13485:2016 standard in the scope of the medical device industry. This achievement shows Proline's commitment to providing quality products to customers.

2021

January, 2021

Proline's Product at Innovation E-Catalog

Starting January 2021, RI-GHA COVID-19 will be available in the innovation e-catalog section as one of the innovative medical device products to help Indonesia to cope with the spreading of COVID-19.
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