Quinary Clinical Research Pvt. Ltd.

Quinary Clinical Research Pvt. Ltd. Quinary is a budding Clinical Research Organization, largely involved in the end-to-end management of human ethics committees.

Quinary Clinical Research Pvt Ltd
13/07/2026

Quinary Clinical Research Pvt Ltd

Transforming Ethics Review. Accelerating Clinical Research.Multicentre clinical studies shouldn't be slowed down by frag...
29/06/2026

Transforming Ethics Review. Accelerating Clinical Research.

Multicentre clinical studies shouldn't be slowed down by fragmented ethics approvals and repetitive review processes.

With Quinary's e-IRB, research teams can move from multiple independent submissions to a single, centralized digital ethics review platform - bringing together Institutions, Ethics Committees and Investigators in one connected workflow.

Our platform enables:
✔️ Single ethics review for multicentre studies
✔️ Faster approvals and reduced administrative burden
✔️ Real-time collaboration and transparency
✔️ Audit-ready compliance and centralized oversight

One Study. One Review. Faster Research.

This digital transformation empowers Institutions and Researchers to seamlessly align with the Operational Guidelines for Single Ethics Review for Multicentre Research in India, ensuring efficiency, transparency and compliance in multicentre study oversight.

Streamlining Ethics Committee Workflows with e-IRBA comprehensive digital platform designed to streamline Ethics Committ...
22/06/2026

Streamlining Ethics Committee Workflows with e-IRB
A comprehensive digital platform designed to streamline Ethics Committee operations, enabling seamless collaboration, real-time communication, efficient document management, and accelerated review processes. e-IRB empowers researchers, sponsors, and committee members to work together effectively, ensuring regulatory compliance while facilitating faster approvals for clinical research studies.

One Study. Many Sites. One Unified Ethics Review Process.Managing ethics approvals across multiple institutions can be c...
10/06/2026

One Study. Many Sites. One Unified Ethics Review Process.
Managing ethics approvals across multiple institutions can be complex and time-consuming. With e-IRB, multicentre clinical studies can streamline ethics review workflows, improve coordination among participating sites, and enhance regulatory compliance across India.
✔ Centralized oversight
✔ Efficient communication across sites
✔ Standardized review processes
✔ Faster study activation
At Quinary Clinical Research, we are committed to leveraging technology to make research governance more efficient and transparent.

We’re delighted to welcome Selva Sundaravel S as Director – Clinical & Regulatory Affairs at Quinary Clinical Research P...
03/06/2026

We’re delighted to welcome Selva Sundaravel S as Director – Clinical & Regulatory Affairs at Quinary Clinical Research Pvt. Ltd. His expertise will strengthen our commitment to excellence, innovation and growth. We look forward to this association as we continue advancing our mission and delivering greater value to our clients and stakeholders.

DSMB Services at Quinary Clinical Research (QCR) With the latest ICMR Operational Guidelines for Single Ethics Review hi...
02/06/2026

DSMB Services at Quinary Clinical Research (QCR)
With the latest ICMR Operational Guidelines for Single Ethics Review highlighting the importance of Data and Safety Monitoring Boards (DSMBs) where appropriate, QCR is ready to support your clinical research needs with comprehensive DSMB management services.

Our DSMB Expertise:
✔ DSMB Constitution & Member Management
✔ DSMB Charter Development
✔ COI & Confidentiality Management
✔ Safety Data Review Coordination
✔ Meeting Management & Documentation
✔ Recommendation Tracking & Reporting
✔ Regulatory-Compliant Archiving

A robust DSMB helps protect participant safety, maintain study integrity, and enable informed decision-making throughout the study lifecycle.

QCR – Delivering Independent, Efficient & Compliant DSMB Solutions for High-Quality Clinical Research.

QuinaryClinicalResearch DataSafetyMonitoringBoard “From Safety Review to Study Success — QCR DSMB Services."

QCR’s Ecosystem – Enabling Efficient Single Ethics Review for Multicentric Studies As part of ongoing regulatory reforms...
25/05/2026

QCR’s Ecosystem – Enabling Efficient Single Ethics Review for Multicentric Studies

As part of ongoing regulatory reforms to accelerate clinical research approvals in India, the Indian Council of Medical Research (ICMR) has released operational guidance on the Single Ethics Committee (EC) Review mechanism for multicentric studies on International Clinical Trials Day.
This guidance is a significant step toward:
✔️ Reducing approval timelines
✔️ Minimizing duplication in submissions
✔️ Streamlining protocol amendment reviews across participating sites
The framework emphasizes:
🔹 Harmonized EC review processes
🔹 Digitized submission & communication systems
🔹 Coordinated review mechanisms between Central ECs and local ECs
🔹 Improved transparency, compliance & oversight

🚀 Future-Ready Digital Support from QCR With future-ready digital capabilities, QCR’s eIRB ecosystem and experienced Ethics Committee support team are well-positioned to support institutions, sponsors, CROs, and investigators in adopting this evolving regulatory model effectively.
The QCR eIRB platform — already supporting multiple multicentric studies and having processed 13,000+ research applications — enables:
✅ Single-Window Submission
Submit one harmonized protocol along with all site-specific documents through a unified digital platform, minimizing duplication and administrative burden.
✅ Centralized Coordination
Facilitates seamless communication between the Coordinating PI (c-PI), participating sites, and reviewing ECs for synchronized study ex*****on.
✅ Accelerated Review Timelines
Automated workflows, structured review pathways, and real-time query management help enable faster ethics review and approvals.
✅ Complete Lifecycle Tracking
Track submissions, approvals, amendments, continuing review activities, and decisions with full transparency and audit-ready documentation.
✅ Enhanced Compliance & Participant Safety
Integrated modules for:
• SAE reporting
• Protocol deviations
• CAPA management
• Continuing review
…help strengthen oversight and participant protection.

💡 Outcome
✔️ Reduced timelines
✔️ Improved regulatory compliance
✔️ Enhanced transparenc

On this special day, I celebrate the courage and commitment of those who participate in clinical trials. Your efforts ar...
20/05/2026

On this special day, I celebrate the courage and commitment of those who participate in clinical trials. Your efforts are essential in advancing medical knowledge and improving patient care.🙏

A perfect blend of review, recognition, and team bonding.✨
06/04/2026

A perfect blend of review, recognition, and team bonding.✨

All Study Files. One secure place 🔐
09/03/2026

All Study Files. One secure place 🔐

Address

Top Floor B Portion, Nandanam Building, No. 1, B Channasandra, OMBR 5th Main Road
Bangalore
560043

Opening Hours

Monday 10am - 6am
Tuesday 10am - 6am
Wednesday 10am - 6am
Thursday 10am - 6am
Friday 10am - 6am
Saturday 10am - 6am
Sunday 10am - 6am

Telephone

+919740233593

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