ABOUT US

C-TrialPro is a Clinical Research Site Solutions Organization for global biopharmaceutical sponsors to optimize drug development. Deploying best-in class clinical research site solutions that deliver efficient, predictable, auditable and ethical clinical trials.

Creation of scalable technology platforms to access clinical research sites and patient networks in emerging markets. Partnering with networks of hospitals, doctors and patients, C-TrialPro helps create an ecosystem for pharmaceutical research and better health.

Global Reach

Access to emerging markets

Advanced Technology

Scalable platforms

Ethical Practices

Highest standards maintained

Expert Team

Experienced professionals

SERVICES & SOLUTIONS

What do we offer and Why Us?

Site Management

We have all the best sites all over India and we manage them very efficiently

Study Feasibility

Have any study? Always contact us to get the Feasibility done at the earliest.

Biospecimen Collection Study

CTrialPro is your best trusted partner for Biospecimens

Institutional Ethics Committee Formation

We are helping in forming Institutional Ethics Committee for various hospitals

Regulatory

We handle all the Regulatory part and ethical issues with ease

GCP Workshop

We are organizing GCP training Workshops in various institutes and hospitals

BIOSPECIMEN COLLECTION SERVICES

Our comprehensive biospecimen collection service supports pharmaceutical research and clinical trials with the highest quality standards. We provide reliable access to various types of biospecimens, ensuring proper collection, processing, and storage.

Comprehensive biospecimen collection services
Full regulatory compliance
Rapid processing and delivery
Expert consultation on collection requirements
Rigorous quality control processes
Secure handling and storage protocols
Detailed documentation and tracking
Global logistics network

CAREERS

We’re always looking for talented professionals to join our team.

Please click the button below to submit your CV (PDF, max 1MB):

Submit Your CV

SITE MANAGEMENT ORGANIZATION (SMO)

We dedicate ourselves to quality and efficiency in clinical research. Our expertise spans diverse therapeutic areas, ensuring successful trial outcomes through strong partnerships.

Site selection and feasibility assessment
Investigator and site staff training
Study start-up and initiation
Ongoing monitoring and oversight
Data management and quality control
Regulatory compliance and documentation
Patient recruitment and retention
Site close-out and study termination

Proven Expertise

Commitment to quality across diverse therapeutic areas.

Collaborative Approach

Working closely to achieve optimal trial outcomes.

Innovation Driven

Leading with technology for clinical research excellence.

EXPLORE OUR ENGAGING COURSES

We believe that learning should be an exciting journey! Discover our specialized diploma program.

Clinical Research & Pharmacovigilance Course

Advance Diploma in Clinical Research & Pharmacovigilance

Master the essentials of clinical trials, data management, and drug safety.

What You'll Learn:

Module 1: Introduction to Clinical Research & Advancement of ICH-GCP
Module 2: Ethical & Regulatory Aspects of Clinical Trials
Module 3: Operations Aspects of Clinical Trials
Module 4: Pharmacovigilance at Glance
Module 5: Signal Management, ADR Reporting System & Dictionaries
Module 6: Regulatory Aspects of Pharmacovigilance
Module 7: Career orientation and Interview Preparation

View Full Syllabus Enroll Now

C-TrialPro

Site Management Organisation