About Us

Vivo Bio Tech is a full service CRO offering drug development & discovery services to pharmaceutical & biotech companies world-wide in accordance with OECD, AAALAC & IND guidelines. The company offers services in the areas of In vitro, In vivo, toxicity studies, pharmacological investigations, pharmacokinetics & toxicokinetic studies etc. Our experienced & talented scientists offer advice on defining drug development paths tailored to specific molecules. Tailored and dedicated to our clients, we distinguish your development plan is as superlative as the products you bring to our testing facilities.

The Biologic Research Services group at Vivo Bio Tech offers a complete line of protein services, including gene synthesis, cloning, expression and purification of recombinant proteins and monoclonal antibodies. Our scientists will team up with you to develop solution for the most difficult to deal products including purification of untagged & poorly expressed proteins.

In-vitro Services offers solutions for pharmacologic, toxicological & bioanalytical investigations in drug discovery & development. Critical investigations like bacterial reverse mutation assays, chromosomal aberration, and micronucleus are specialty services by our scientists.

The In-vivo Services group at Vivo Bio Tech provides both non-regulatory and regulatory IND enabling preclinical development services. We are capable of screening & evaluating molecules for various pharmacological & therapeutic properties. Specifically for oncology, our scientists can provide design & development of xenograft models for evaluation of anti-cancer agents. Further, our scientists can customize in-vivo DMPK studies to help profile your drug candidate in both rodent and non-rodent animal models.

Vivo Bio has partnered with Taconic for sourcing foundation and expansion colonies of the animal models and have started in-house breeding of Specific Pathogen Free rodents.

Why Vivo Bio Tech?

Vivo Bio Tech offers pioneering methodologies for support backed by precise service level agreements to ensure comfort of client through the period of the study & thereafter. We have very experienced scientists with proven capabilities in drug development. We have a sophisticated facility in this region. The following are the advantages of partnering –

Highest Quality Standards

At Vivo Bio Tech, we believe that a client requires delivering confirmable results for all regulatory studies, hence, all the study procedures are developed and validated to meet current GLP and ICH guidelines. The scheme of quality assurance available at Vivo Bio Tech strongly adheres to the requirements of OECD and FDA regulations.

Regulatory support services

Our teams of experts have proven expertise for moving lead candidates to IND and subsequent market approval. Our experts can suggest you the suitable research options enabling you quick turn-around submissions to regulatory agencies.

End-to-End Integrated Services

We offer broad range of services ranging from In vitro to preclinical development addressing the full service lifecycle, both within and beyond the studies.

Fast Turn around Time

With the all the infrastructure located in vicinity, all the Biologic Research, in-vitro and in-vivo services requirement of the sponsor is addressed, thereby minimizing cost and turn-around time.

Seamless facility operations

With iBMS system, our facility is under constant monitoring & surveillance for all the activities being carried out. With restricted entries to personnel to different areas of the buildings based on their predefined roles, our facility defines the right environment to carry out all your research needs.

Cost effectiveness

Owing to the location benefit (Asia-Pacific), Vivo Bio Tech offers cost effective solutions within the stipulated time lines without compromising on the quality of deliverables