Our Services
Clinical Operations
From Study Start-Up to Close-Out - Efficient, Compliant & Quality-Focused Clinical Trial Operations
Ethics Committee Registration & Administration
Build a Compliant, Effective & Inspection-Ready Ethics Committee.
NABH Accreditation of EC and Clinical Sites
Strengthen Quality. Demonstrate Compliance. Build Assessment Readiness.
Human Resource
Building Skilled, Trained & Compliant Clinical Research Teams
Third Party Archival
Professional Archival Solutions for Clinical Research, Ethics Committees, Hospitals & Research Organizations
Day-to-day management of a trial site, from first contact through to close-out. This includes site selection support — market research, surveys, and interviews with physicians and medical staff to confirm a site is right for the study — along with feasibility assessment, subject recruitment, patient care, and subject retention through effective follow-up and ancillary care. Our team handles the operational load so sponsors and investigators can focus on the trial’s scientific outcomes.
- Site Selection Support
- Feasibility
- Contract & Budget Assistance
- Study Staff Training
- Site SOP Preparation
- IRB / IEC Related Process
- Informed Consent Process
- Subject Recruitment
- Patient Care
- Subject Retention
- Drug Dispensing & Accountability
- Adverse Events
- Site Master File Maintenance
- IP Management
- Case Report Forms
- Monitoring & Auditing
- Study Close-Out
- Archival
End-to-end support for working with Institutional Review Boards and Ethics Committees, including assistance for faster submission and approval. This extends to the informed consent process — every subject enrolled has the right to understand every detail of the trial they’re joining, and our experienced study staff manage that process directly, along with the ongoing administrative work an Ethics Committee requires to stay compliant.
GCP (Good Clinical Practice) and study-specific training delivered to every member of study staff by our experts. We appoint experienced Clinical Research Coordinators (CRCs) and study managers at each site, trained to ensure smooth, compliant conduct of the trial from day one.
We support Ethics Committees and clinical sites in working toward NABH accreditation standards. This includes reviewing existing documentation, processes, and site practices against what NABH requires, and helping strengthen the gaps we find. Our team stays involved throughout the process, working alongside site staff rather than simply flagging what needs to change. The goal is a smoother, better-prepared path to accreditation, with fewer surprises along the way.
We help identify, place, and support qualified clinical research staff at your study site. This includes coordinating staffing needs so the right people are in place before a trial begins, not scrambling to fill gaps once it’s underway. Staff placed through CliniGlia are expected to meet GCP and study-specific requirements for the duration of the trial. We stay involved throughout the study rather than stepping back after initial placement, so staffing issues get handled quickly if they arise.
Once a study closes out, all trial documentation needs to be retained securely for as long as regulations require — often for several years after a trial ends. We provide third-party archival facilities with the required measures and provisions in place to keep those records safe, organized, and retrievable. This includes physical storage, protection from damage or loss, and a clear system for locating specific documents if a sponsor, auditor, or regulator needs access later.
Clinical Operations
Our Clinical Operations Services and Training Programmes support the complete clinical trial lifecycle—from study planning, site selection and start-up to participant management, monitoring, quality oversight, and study close-out. We help Sponsors, CROs, hospitals, and clinical research sites strengthen GCP compliance, protocol adherence, participant safety, documentation, data integrity, and overall trial quality.
Ethics Committee Registration, Administration​
Build a compliant, effective, and inspection-ready Ethics Committee with expert guidance on CDSCO and DHR registration, EC administration, SOPs, documentation, review processes, training, and regulatory compliance. Our practical training and consultancy services support hospitals, medical colleges, universities, research institutions, and professionals in establishing and managing well-structured Ethics Committees aligned with applicable regulatory and ethical requirements.​
NABH Accreditation of EC and Clinical Sites
Our NABH-focused training and consultancy services help Ethics Committees, clinical research sites, hospitals, medical colleges, and research institutions strengthen quality management, documentation, governance, and compliance systems. We help organizations develop structured and sustainable quality systems aligned with NABH requirements, supporting assessment readiness, continuous quality improvement, and effective clinical research governance.​
Human Resource
Our Human Resource Services for Clinical Research help hospitals, medical colleges, research institutions, and clinical trial sites build skilled, trained, and compliant research teams. We support the complete HR lifecycle—from manpower planning, recruitment, qualification assessment, and training to deployment, performance monitoring, competency development, and retention—ensuring clinical research teams are equipped to meet GCP, regulatory, protocol, documentation, and participant safety requirements.
Third Party Archival
Our Third-Party Archival Services provide secure, structured, and compliant long-term storage of clinical research, regulatory, Ethics Committee, and institutional records. We help organizations maintain documents with confidentiality, controlled access, traceability, document integrity, and easy retrieval, supporting regulatory requirements and inspection readiness while reducing the burden of managing archival infrastructure internally.