clinical research services

preclinical research services

BA / BE studies

Training Institute

Data management

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Study Feasibility

Clinical research study feasibility assesses participant availability, resources, and compliance to ensure successful study execution. Key factors include demographics, facility and staffing adequacy, ethical/regulatory approvals, and financial/logistical considerations.

Clinical monitoring

Clinical monitoring ensures a clinical trial adheres to the protocol, GCP, and regulatory requirements, safeguarding participant well-being and data integrity. It involves regular oversight, data verification, and compliance checks.

Site management

Site management in clinical research ensures trial sites adhere to protocols, regulations, and GCP, overseeing staff training, patient recruitment, and data collection. It involves regular performance monitoring and coordination of site activities.

Data management

Data management in clinical research involves collecting, processing, and ensuring the quality and integrity of data throughout a clinical trial. This includes data entry, validation, storage, and maintaining compliance with regulatory standards to ensure accurate and reliable study results.

Our Mission

Our mission is to conduct clinical research studies that help pharmaceutical companies develop new medications and new indications for existing medications for a variety of disorders over a wide spectrum of clinical areas. At the same time, helping our patients and clinical trial participants discover new and effective therapies for their conditions where other existing therapies have been unsuccessful.

Our Vision

Our vision is to provide quality and accurate clinical research to help advance tomorrow’s medicines today & Our dedicated and experienced multidisciplinary team of physician’s conducts clinical research with integrity and respect to our clinical research participants.

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Our Members

Our Collaborated Sites

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Our Clients

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Our Certifications