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Prothix Lifesciences
Prothix Lifesciences
Where Research Meet Outcomes !

Unlock Clinical Trials, Medical Affairs, Toxicology & Pharmacology Services to Enhance Your Product Claims Positioning !

Maximize your business with our proven approach (BX) by partnering with us for unparalleled R&D success.

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Our Achievements

125+

Clients

300+

Projects

667+

Sites

900+

GCP Trained PI's

100+

Publications

Type Of Industries We Serve

Pharmaceuticals


Biotechnology

Medical Device

Nutraceuticals

Functional Services

Clinical Research

ICH-GCP Complain Phase II - IV clinical trials

Medical Writing

Manuscripts to CES writing for publication or MAH submission

Pharmacology

In-vivo Efficacy and dose Response Studies in rodents 

Toxicology

in-vivo & In-vitro LD50 and MTT assays in laboratory & Vivarium

Bioavailability

Crossover and Parallel BE/BA Studies as per MAH 

In-Vitro Studies

Bioassays and Potency Testing in non-GLP & GLP environment

Bio-Repository 

Biobanks & Tissue banks for Research Purpose 

Drug Safety & PV

Lifecycle management of the drug including PSUR, SUSUR and RBR

20+ SOC

Partner With Us To Build a Resilient R&D Business

Prothix Lifesciences has been conceived as an extension of the innovative and research-driven principles established by Ethix Pharma. Building upon the strong foundation and industry expertise developed at Ethix Pharma for 17+ years, Prothix Lifesciences emerged to further specialize in clinical and preclinical research services. 

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ICH-GCP Complaint

Quality & Complainces 

We are among the few GCP-compliant CROs that are fully aligned with the FDA, FTC,NDI, EFSA, CDSCO, FSSAI, AYUSH standards for human studies.

Recognized By DIPP Via Certificate No. DIPP174243

Recognized Start-up by the Department for promotion of industry and internal trade in "Healthcare & Lifesciences" for "Healthcare Services"

ISO 9001:2015 IMS for QMS

Integrated Management Systems (IMS) is a holistic approach that harmonizes various management systems within an organization to address objectives collectively. Instead of treating processes individually, IMS ensures a seamless integration, fostering efficiency, reducing costs, and minimizing external audit disruptions.

ICH-GCP E6 (R2)

This document addresses the Good clinical practice

A code of international standards concerning the design, conduct, performance, monitoring, auditing, recording, analysis and reporting of clinical trials. Good clinical practice provides assurance that a study’s results are credible and accurate and that the rights and confidentiality of the study subjects are protected.

Quality | Awards | Recognition

The success of a clinical trial is driven by the strategic selection of a reliable CRO. Our vastly experienced team of highly qualified professionals, a comprehensive portfolio of clinical research services to support diverse requirements, and a robust Quality Management System guided and nurtured by our quality culture makes us a partner of choice for some of the leading pharmaceutical companies in the world.