OUR VISION
To become a leader in the field of Pharma,Biotech,bio/Chemo informatics,ADEMT-clinical research for drug development and  be a renowned source for the highest quality on science with ethics.

OUR MISSION
Committed to meet the international standards through continuous training and development.

OUR PROMISES
We will be your best choice for:
Cost Effectiveness \ Timely Delivery \ Adherence to Regulatory Complaince \ Efficient Project Management

CHROMOSOFT is one of the Global leading providers of BIO,Pharma CRO/KPO Training dedicated to promoting ethical and high- quality Multi Research. Recognizes the need for well-trained Pharma,clinical researchers to bridge the gap between the basic researcher’s bench. Chromosoft is committed to result oriented, effective, dedicated management of Pharma clinical research training in India.

Indian Healthcare industry has been facing daunting challenges addressing the imbalance in the demand and supply of skill and talented work force. The CROs & Pharmaceutical company of the Healthcare world have been pumping huge amounts for the in-house training program essential for grooming the professional in line with industries’ growing requirements.

CRC - BIO provides contract research services in biology to a growing base of biotech and pharmaceutical companies’ world wide. Biological evaluation of New Molecular Entities (NMEs) plays crucial roles in ascertaining structure activity relationships [(SAR) to correlate chemical structure with biological activity], potency, ADME and in vivo efficacy assessment.

The scope of Biology services encompasses in vitro and in vivo profiling of molecules for their efficacy, ADME and toxicity. The Biology services at CRC-BIO complement our existing strengths in Medicinal Chemistry, Bioinformatics and Clinical research. Our integrated services platform allows clients to access multiple and seamless outsourcing choices across the drug discovery chain, ensuring speedy implementation of their research projects.

Our Biology strengths have been capitalized on the development of screening methodologies based on advanced technological platforms, developing a strong scientific team and to perform in an environment that meets international standards.

Require new ways of working and we believe that to deliver the true promise of BIO sciences, innovation is necessary. Our clients benefit not just from lower costs and boosted efficiencies, but also from the infusion of fresh ideas and thinking. Our location allows us easy access to a diverse talent pool .

Understanding the specific needs of Clinical Trials & Research,CRC group has set up a Clinical Research Services unit to provide dedicated facility in this field. The Clinical Trials Safety Laboratory meets international standards, can handle high volume workloads, provides a secure and safe environment for sample storage and an advanced laboratory information management system. It is located close to the international and domestic airports for faster sample management.

For further details contact clinical.trials@crcgroupin.com

Client specific Project Managers are designated to provide personalized services. Highest priority is given to client confidentiality. The Clinical Research Services can customize all its processes and functions to the needs of the client. With the advent of clinical trial outsourcing to Asia, CRC looks forward to an exciting business partnership with our overseas clients in the near future. CRC has a rich working experience of over years as a reference laboratory and is one of the highest accredited laboratories in the Global. We are committed to provide quality central laboratory services for clinical trials, understanding fully that the reliability of clinical laboratory data is crucial for the success of each trial. We maintain the integrity and confidentiality of your research which is critical to the well being of each study subject and overall success of the trial. The lab provides services that meet the required regulatory standards of the pharmaceutical industry. In last five years we have offered our services as central laboratory for clinical trials to most of the leading national and international pharmaceutical companies.

QUALITY ASSURANCE

The laboratory has a well documented Quality Assurance (QA) program based on good laboratory practices (GLP). We perform testing in the laboratory using standard operating procedures and world class equipment. Our Quality Assurance team understands that accurate clinical data is key to maintaining the integrity of your research and for the well-being of each subject.

STRATEGIC PROJECT

Clinical Trials Strategic Project Managers carefully review study protocols prior to having an initial central laboratory services discussion with the study sponsor. He/she will also discuss protocol revisions with the study sponsor, address sponsor satisfaction concerns throughout the duration of the study partnership. The option of customized test request forms and reporting formats is also available.