ICBio Clinical Research Pvt. Ltd. is a premier, full-service clinical research organization headquartered in Bengaluru, India. We deliver end-to-end, high-quality clinical research solutions to pharmaceutical and biopharmaceutical companies worldwide, ensuring regulatory compliance and scientific excellence.
ICBio is a full-service clinical research organization established by experienced clinical research professionals to provide high-quality, scientifically driven, and cost-effective research solutions. Based in the heart of Bengaluru, India, we support domestic and international pharmaceutical and biopharmaceutical companies across the complete spectrum of clinical research and drug development.
As a dedicated clinical research organization in Bengaluru, we ensure the highest standards of ethical conduct, data integrity, and scientific excellence. Our comprehensive expertise covers Bioavailability/Bioequivalence (BA/BE) studies, clinical trials from Phase I to Phase IV, bioanalytical research, pharmacovigilance, regulatory services, medical writing, biostatistics, clinical data management, and central laboratory services.
We are deeply committed to advancing clinical research in India by maintaining rigorous quality standards. Our state-of-the-art facilities in Bengaluru are designed to meet the demands of global drug development programs, ensuring timely delivery and regulatory compliance for every sponsor we partner with.
As a premier clinical research organization, ICBio delivers end-to-end clinical research services across BA/BE studies, clinical development, bioanalytical research, regulatory services, and central laboratory solutions, all managed from our Bengaluru facility.
End-to-end BA/BE study solutions for generic and pharmaceutical products in India, from study planning and volunteer management to data generation and regulatory reporting.
Advanced bioanalytical services supported by modern LC-MS/MS instrumentation and validated analytical methods for pharmaceutical research at our Bengaluru laboratory.
Clinical research support across Phase I to Phase IV studies in India, including healthy volunteer and patient-based research programs managed by expert teams.
Professional statistical planning, analysis, programming, and reporting to support clinical research and regulatory submissions for global health authorities.
Regulatory support designed to help sponsors navigate submission requirements and meet applicable national and international regulatory expectations seamlessly.
Safety monitoring and pharmacovigilance solutions supporting the identification, assessment, documentation, and management of safety information globally.
Scientific and regulatory medical writing services for clinical and pharmaceutical research documentation across global markets, ensuring clarity and compliance.
Structured clinical data management solutions designed to maintain data quality, consistency, integrity, and regulatory compliance throughout the trial lifecycle.
A fully integrated central laboratory supported by LIMS, NABL accreditation, GCLP compliance, and advanced analytical capabilities in our Bengaluru facility.
ICBio has extensive experience supporting studies approved or accepted by regulatory authorities and health agencies across multiple international markets.
India
Brazil
Chile
Malaysia
United Kingdom
Europe
Australia
UAE
Iraq
Gulf Council
Kazakhstan
Zambia
Choosing the right clinical research organization is critical for your drug development success. ICBio provides the regulatory experience, accredited laboratories, and data integrity you need.
Studies approved or accepted by DCGI-CDSCO, ANVISA Brazil, ISP Chile, NPRA Malaysia, MHRA, EMA, TGA, UAE MOH, Iraq MOH, GCC, Kazakhstan, and Zambia.
Our central laboratory in Bengaluru is supported by NABL and ILAC-MRA accreditation and follows applicable quality and compliance standards.
Our research and development capabilities are supported by DSIR approval from the Government of India, ensuring top-tier scientific validation.
Dedicated project management teams coordinate research activities and maintain clear communication with sponsors throughout the study lifecycle.
Our network includes approximately 150 hospital and investigator sites across 17 cities in India, facilitating rapid patient recruitment.
Accurate, reliable, comprehensive, and scientifically sound data while following applicable ICH-GCP and regulatory requirements.
Our clinical research organization operates a purpose-built clinical research infrastructure in Bengaluru covering approximately 20,000 sq. ft., designed to support complex and multi-study requirements with the highest level of precision.
20,000 sq. ft. facility featuring clinical units, volunteer screening areas, volunteer information centres, and secure archival infrastructure.
Advanced instrumentation including SCIEX 4000, SCIEX 4500, SCIEX 5500, Shimadzu 8040 and 8050 mass spectrometers, and PerkinElmer ICP-MS.
Air-conditioned clinical research units with controlled access, ICU support, UPS backup, and 24/7 medical support availability.
Our team has developed and validated methods for 200+ molecules, supporting diverse pharmaceutical research requirements globally.
Central laboratory supported by NABL and ILAC-MRA accreditation, following GCLP compliance and applicable quality standards.
Headquartered at Devi Circle, Chikkabettahalli, Yelahanka Main Road, Bangalore – with excellent connectivity and infrastructure.
A streamlined, quality-driven approach designed to support your development and regulatory objectives efficiently from our Bengaluru headquarters.
We understand your product, research objectives, regulatory requirements, and project timelines.
Our experienced scientific and project management teams develop a customized research approach aligned with your requirements.
Studies are conducted through experienced professionals, quality systems, advanced infrastructure, and appropriate regulatory procedures.
Scientific, clinical, bioanalytical, and statistical data are processed and reviewed with accuracy, ensuring reliable and timely research outputs.
We provide customized research solutions to support innovator, generic, and biosimilar development programs across domestic and international markets from our base in Bengaluru, India.
As a leading clinical research organization in Bengaluru, ICBio proudly serves pharmaceutical, biopharmaceutical, and medical device companies across major localities in Karnataka and pan-India. Our strategic Bengaluru location ensures seamless collaboration with top-tier hospitals, investigator sites, and regulatory bodies.
ICBio is committed to becoming a preferred research partner for organizations involved in drug development and healthcare innovation worldwide.
"ICBio's experienced team and scientific expertise provide valuable support throughout the clinical research process, helping sponsors manage complex study requirements efficiently."
— Pharmaceutical Research Partner
"The combination of experienced professionals, advanced infrastructure, and regulatory knowledge makes ICBio a dependable partner for clinical research programs."
— Biopharmaceutical Client
"ICBio maintains a strong focus on data quality, timelines, communication, and sponsor requirements throughout the study lifecycle."
— Global Healthcare Client
Learn more about how ICBio, a premier clinical research organization in Bengaluru, can support your drug development and regulatory submission needs.
ICBio offers comprehensive clinical research services in Bengaluru, including Bioavailability/Bioequivalence (BA/BE) studies, Phase I to Phase IV clinical trials, bioanalytical research, pharmacovigilance, regulatory services, medical writing, biostatistics, and clinical data management.
Yes, our central laboratory in Bengaluru is fully NABL and ILAC-MRA accredited, ensuring the highest standards of data integrity, GCLP compliance, and regulatory acceptance globally for all bioanalytical and clinical research projects.
ICBio has extensive experience supporting studies approved or accepted by DCGI-CDSCO (India), ANVISA (Brazil), MHRA (UK), EMA (Europe), TGA (Australia), NPRA (Malaysia), and several other global health agencies.
Partner with ICBio for high-quality, scientifically sound, regulatory-compliant, timely, and cost-effective clinical research solutions trusted by 90+ clients across 56+ countries.
Request a Consultation →Looking for a reliable clinical research organization partner for your pharmaceutical, biopharmaceutical, medical device, nutraceutical, or clinical research program in Bengaluru or India? Connect with ICBio today.
#2, Survey No. 8/1/2, ICBio Tower 2, Devi Circle, Chikkabettahalli, Vidyaranapura, Yelahanka Main Road, Bangalore – 560097, India
+91-80-23641042 / 43
+91 9900111990 (Mobile)