Exemplary Preclinical Contract Research Organization!!!.

A preclinical and biological contract research organization, SyncBio Research Private Limited (SBR) began operations in 2019 with the goal of offering top-notch preclinical services. Growing with the times, SyncBio Research Private Limited (SBR) has put in place quality systems that adhere to CCSEA, FDA – GoG, Schedule L1 GLP, ISO/IEC 17025:2005,  and other regulations.

 

With its cutting-edge testing facilities and laboratories situated in a tranquil setting, SBR has been offering testing services for Toxicology, Pharmacology, DMPK, Biocompatibility/Biological Reactivity, and Pharmacopoeia to companies in the pharmaceutical, biopharmaceutical, medical device,  and various research institutes.

 

SBR boasts cutting edge facilities and laboratories spanning 6,000 square feet. Animal facilities and laboratories are outfitted with modern technology that keeps up with the most recent developments in science.

 

SBR is cognizant of the significance of its clients’ projects hold a position, and it can provide you with reports that are of the highest caliber by adhering to stringent quality control procedures and meet industry requirements in a timely manner. SBR continues to assist long after the project is finished.

 

SBR’s highly skilled and informed personnel offers timely, polite, and courteous services. The helpful management further improves this.

 

SBR can give end-to-end solutions and optimize the success of your endeavors owing to our professional approach and in-depth knowledge of your initiatives.

 

We Thank GSBTM and i-HUB    for their support and assistance

Our Range - Services

Pharmaceuticals / Biopharmaceuticals

SyncBio Research Pvt Ltd offers Bioassay Services (IP/BP) as well as Toxicity/Batch release services (IP/BP/USP)

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Preclinical & Toxicological

The mission of SyncBio Research is to support the preclinical and development of biologics, biosimilars, peptides, protein medicines, vaccines, and other innovative biologics therapeutic products.

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Biocompatibility Studies for Medical Devices

Biocompatibility Studies are conducted as per ISO/IEC 17025: 2005 for the testing of medical devices. In accordance with ISO, US FDA, and regulatory approval criteria for CE marking, our team of highly qualified scientists thoroughly…

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Risk Assessment

The published and proprietary toxicological data for the drug of interest and surrogate molecules are being thoroughly evaluated in order to undertake hazard analysis, assist product regulatory compliance, and perform product safety risk assessment

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Laboratory Animal Supply

We are aware that choosing the right animal model for your investigation is essential to its pre-clinical success. Animal models of the highest caliber, including mice, rats, guinea pigs, hamsters, and rabbits, are what SyncBio is dedicated…

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