Clinical Trial Services
Elevate your biotech research with Celero's comprehensive clinical trial services, guided by a team that emphasizes safety and unmatched standards.
Celero Comprehensive Clinical Trial Services.
From Concept to Completion.
Celero is your trusted partner for Clinical Trial Services, providing high-quality, cost controlled, and efficient solutions tailored to biotechs unique needs. Trust us to help navigate your journey through the complex world of clinical trials.
Clinical Trial Project Management
Our experienced project management team outlines the work, budget, resource, scope, and timeline. They execute and oversee the clinical trials from setup to closure, ensuring successful completion within the planned parameters.
Site Feasibility
Our team ensures the clinical investigative site is qualified to participate in the trial. Factors such as site staff availability, infrastructure, regulations, and cost-effectiveness are carefully considered to ensure the smooth execution of your trials.
Clinical Trial Application
We prepare and submit the clinical trial documents to Regulatory Authorities (RA), Central Ethics Committees and Independent Review Boards/Ethics Committees (IRB/IEC), ensuring you receive authorization to conduct the clinical trials as per the requirements.
Site Monitoring
Our site monitoring services verify that your trials are conducted in compliance with the study protocol, Good Clinical Practice (GCP), and with the applicable regulatory requirements. We ensure data correctness and accuracy and prioritize subjects' rights and well-being.
Project Specific Training
We provide the information and knowledge needed to conduct the trial correctly. Our training complies with the protocol and regulatory requirements for both our team and the site staff.
Clinical Trial Supply Services
Our clinical supplies management ensures the accurate supply of the investigational products used in the trial. We oversee accurate accountability from receipt, storage, to dispensing according to the requirements.
Biological Sample Handling
Our team verifies that biological samples are collected, stored, and transported to the laboratory according to the protocol requirements and laboratory instructions.
Trial Master File (TMF) Management
We manage and maintain your Trial Master Files (TMF) to demonstrate that the clinical trial has been conducted in compliance with the protocol, GCP, and Regulatory requirements.
Budget Management
Our budget management services focus on the planning, allocation, monitoring, and control of financial resources throughout the lifecycle of a clinical trial. We ensure that your clinical trial is conducted within the approved budget.
Regulatory Audit / Inspection Readiness
In collaboration with our Quality Assurance team, we maintain compliance with the protocol, GCP, and applicable regulatory requirements throughout the course of the clinical trial. We prepare for potential audits or inspections, ensuring readiness at all times.
Global Coverage
Celero Executive team have experience in 80 trials across multiple clinical development phases (P1-P4) in more than 29 countries (US, EU, LATAM, APAC and Africa).
Introducing the Celero Way
A pathway to high-quality, cost-controlled, accelerated trials tailored to your needs.
Learn more about The Celero Way or speak to our Clinical Trial expert.
Speak to an Expert
Speak to an Expert
We are successfully ISO 9001 certified, which further underscores our commitment to meeting internationally recognized quality standards for quality, reliability, and excellence.