Our Approach
At our clinical research site, we take a comprehensive and collaborative approach to conducting research studies. We understand the importance of conducting rigorous and ethical research to advance scientific knowledge and improve patient care. Our team of experienced researchers, clinicians, and support staff work together to design and implement studies that meet the highest standards of quality and safety. We prioritize patient-centered care and strive to create a comfortable and welcoming environment for study participants. We also value transparency and communication with our sponsors, regulatory agencies, and the broader scientific community. By adopting a multidisciplinary approach and staying up-to-date with the latest advancements in clinical research, we aim to make meaningful contributions to the field and ultimately improve patient outcomes.
Our Facility
Our spacious facility currently has 2000 sq feet of working area and includes:
-Two Private Exam Rooms
-Dedicated Coordinator's Rooms
-Dedicated offices for Monitors and Sponsor to use
- Ample Patient's Waiting Room
-Secure and double locked Storage Area
-Secure and double locked Pharmacy
- Dedicated and double locked Laboratory Area
- Dedicated Regulatory lock regulatory Area
- Reserve parking spaces
- Handicap accessible restrooms
Our Capabilities
-CLIA Waiver Certification
- Secure Ambient cabinets, Refrigerators, -20 and -80 Freezers
- 24/7 Electronic Temperature Monitoring System with Min and Max
monitoring recording and SMS and e-mail notifications
- Two Standard centrifuges for a faster flow of Subjects
- ECG machines
-AED Equipment in Office
-Body Weight scale
- Laboratory State of the Art Scale
-Viral Signs Electronic Monitoring Equipment
- High speed wireless internet access throughout
- Storage is kept locked at all times and is only accessible to assigned clinical personnel. Limited access is strictly enforced with state of the art locks
- 24/7 monitored security cameras throughout the Building
-Works with local labs for prompt labs results
About Us
Our clinical research site boasts a highly trained and dedicated team of full-time research staff members who specialize in conducting clinical trials. Lead by our P.I. Dr.Tanuj Bhatnagar a well know Pulmonologist and Sleep Apnea Specialist who has expertise in treating Asthma , COPD, Pulmonary Fibrosis among others Our study coordinators possess the necessary qualifications, education, training, and experience, including GCP and IATA certifications, to expertly manage clinical trials, two of them are International medical graduate doctors. In addition, we have a regulatory specialist who oversees all regulatory documentation requirements and submissions, as well as contract and budget staff . Our QA teams ensure that all activities are closely monitored to guarantee compliance with our internal and protocol SOPs and regulations. With our qualified staff, we have the ability to rapidly contract, obtain IRB approvals, and launch new trials, typically within a matter of days.
Data Entry within 24H of Subject Visit
Data clarifications answered within 48H of Receipt
Data clarifications answered within 48H of Receipt
Data clarifications answered within 48H of Receipt
Data clarifications answered within 48H of Receipt
Data clarifications answered within 48H of Receipt
Data Queries resolved within 72H of Receipt
Data clarifications answered within 48H of Receipt
Data Queries resolved within 72H of Receipt
Proficient in
