Welcome to C-Trials Global Inc.
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About C-Trials Global Inc.
C-Trials Global Inc. specializes in comprehensive Clinical Research Solutions, with a strong focus on:
- CT & BA-BE/PKPD Study Monitoring
- Pharmacovigilance and Patient Safety Review Services
- Medical Monitoring
- Qualification Audit Services
- Clinical Trials Operation Services
- Medical and Scientific writing services
- Formulation and ready dossier services
- Contractual CRA/Staff services
- Complete CRO & Pharmaceutical unit Set Up
- GXP Training (GCP/GLP/GVP/GMP)
- Regulatory and Compliance Services
Expertise:
C-Trials Global Inc. offers a complete portfolio of clinical research services. The company is known for delivering global projects with speed, competency, and cost-effectiveness. It has extensive experience working with diverse territories and organizations across the USA, India, Jordan, Europe, China, Canada, UK, Thailand, and Malaysia.
Capabilities
The team at C-Trials Global Inc. is highly trained and possesses expertise in all aspects of Good Practice (GxP). The company boasts an unmatched combination of knowledge, project management skills, and experience in handling hundreds of bioequivalence studies for various submissions worldwide. This diverse team of professionals, consultants, and subject matter experts enables the company to develop new approaches and capabilities to meet the challenges in the product development life cycle.
Mission
The core mission of C-Trials Global Inc. is to ensure “Quality, Integrity, Commitment.” The company is dedicated to providing the best research data for its clients by adhering to rigorous standards and guidelines.
Compliance and Standards
C-Trials Global Inc. has extensive experience in handling clinical research activities according to various international standards and guidelines, including but not limited to:
- USFDA
- EMA
- MHRA
- ANVISA
- Health Canada
- TGA
- Chinese FDA
- PMDA
- GCC
- New Drugs and Clinical Trials Rules, 2019 – Amendment-2022 (CDSCO)
- Other Asian countries (Indonesia, Thailand, Malaysia, Singapore, etc.)
Conclusion
With its global reach, extensive expertise, and commitment to quality and integrity, C-Trials Global Inc. is a reliable partner for comprehensive clinical research solutions.
C-Trials Global's Services
CT/Bioequivalence/PKPD Study Monitoring
Pharmacovigilance Services
Audit Services
Clinical Trials Operations
Medical Monitoring
Medical And Scientific Writing
Contractual CRA/Staff support
GXP Training
Special Consultation Programs
Formulation & Ready Dossier Services
Regulatory and compliance services
Why Choose C-Trials Global
At C-Trials Global Inc. we believe transparency and flexibility are the keys to success when working with our clients. Our clients and the trials being conducted come in versatile shapes and sizes. We endeavor to meet our clients’ needs by being proactive and have created an environment that advances this approach with our teams. We believe people/clients are our greatest asset and understand that best performances come from individuals who know they are part of an esteemed team.
- Experience with all phases of clinical trials (Phase II -IV) across multiple therapeutic areas, in paper and electronic data environments.
- Highly experienced and responsive team with 20 years’ experience in the pharmaceutical industry.
- More than 200 Sites, 250 PIs, more than 2000 Patients recruited till date.
- Worked with more than 50 ethics committees.
- 24X7 Data Backup
- Well trained and responsible staff (As per USFDA, EMA, MHRA, ANVISA, Health Canada, TGA, Chinese FDA, PMDA, GCC, ICH-GCP New Drugs and Clinical Trials Rules, 2019 – CDSCO and Applicable Regulatory Guidelines)
- Impeccable work record for delivery on time and with best quality.
- End to end Clinical Trial services.
Your Trusted Partner in Clinical Research Excellence
A Global Clinical Research Services Provider
Global Country Presence
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Our Experiences
Years of experience Expert Team
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BA/BE Studies monitored
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Medical Monitoring Projects
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Pharmacovigilance Case processing
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Clinical Trials/PKPD Studies monitored
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GXP trainings and consulting programs
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Call For More Info
+1 (484) 697-8988