Clinical Trials Research Outsourcing Services
Our clinical trials research outsourcing services deliver turnkey solutions from protocol development to final report submission, ensuring data integrity, patient safety, and regulatory acceptance.
Our Clinical Trials Research Capabilities
Our experienced clinical research teams, global site network, and robust project management tools ensure smooth execution of Phase I–IV trials across therapeutic areas and patient populations.
Types of Clinical Trials Research We Handle
- Phase I Safety and Tolerability Trials
- Phase II Proof-of-Concept Trials
- Phase III Pivotal Efficacy Trials
- Phase IV Post-Marketing Surveillance
- Bioavailability and Bioequivalence Studies
- First-in-Human Studies
- Adaptive Design Trials
- Randomized Controlled Trials (RCTs)
- Observational and Epidemiological Studies
- Registry-Based Trials
- Comparative Effectiveness Studies
- Cross-Over Study Designs
- Multi-Center Global Trials
- Pediatric Clinical Trials
- Oncology Clinical Trials
- Vaccine Clinical Trials
- Medical Device Clinical Trials
- Real-World Evidence (RWE) Studies
- Patient-Reported Outcomes (PRO) Studies
- Biomarker-Driven Trials
- Precision Medicine Trials
- Feasibility and Site Assessment Studies
- Patient Recruitment and Retention Programs
- Data Safety Monitoring Board (DSMB) Oversight
- Interim Analysis and Protocol Amendments
- Clinical Trial Data Integration
- eClinical and EDC System Implementation
- Regulatory Submissions and Liaison
- Audits and Quality Assurance
- Custom Clinical Trial Support Services
Key Research Outsourcing Services Offered
- Protocol Development and Review
- Clinical Trial Design Consultation
- Site Identification and Qualification
- Investigator and Site Contracting
- Regulatory Document Preparation
- Ethics Committee Submissions
- Patient Recruitment Strategy
- Informed Consent Process Management
- Clinical Monitoring and Site Visits
- Source Data Verification (SDV)
- Data Management and EDC Setup
- Adverse Event and SAE Reporting
- Medical Monitoring Services
- Safety Data Reconciliation
- Interim Analysis and Data Review
- Biostatistics and Statistical Analysis
- Clinical Study Report (CSR) Writing
- Regulatory Submissions and Filing
- QA Audits and Inspections Support
- Training for Sites and Investigators
- Patient Retention and Engagement Programs
- Vendor and Third-Party Oversight
- Electronic Trial Master File (eTMF) Management
- Risk-Based Monitoring Implementation
- Clinical Data Integration and QC
- Publication Support and Manuscript Drafting
- Secure Data Archiving and Backup
- Post-Study Support and Regulatory Queries
- Custom Long-Term Clinical Partnerships
Why Choose Us for Clinical Trials Research Outsourcing?
Our clinical trial management experts, regulatory knowledge, and global site network ensure cost-effective, timely, and high-quality trial execution with robust patient safety and data integrity.
Industries & Sectors We Serve
- Pharmaceutical and Biotech Companies
- Medical Device Manufacturers
- Clinical Research Organizations (CROs)
- Academic Medical Research Institutes
- Public Health and Regulatory Bodies
- Contract Manufacturing and Logistics Providers
Customized Clinical Trials Solutions
We tailor trial protocols, site management plans, and patient retention strategies to align with your therapeutic area, regulatory goals, and timeline constraints.
Quality Assurance & Regulatory Compliance
Our clinical trial processes comply with ICH GCP, FDA, EMA, and local regulatory guidelines, ensuring audit-ready data, traceability, and regulatory acceptance.
Case Studies & Client Success Stories
Explore how our end-to-end clinical trial services have accelerated product approvals, ensured patient safety, and maintained data quality across diverse studies. References available upon request.
How It Works: Our Research Outsourcing Process
- Requirement Gathering: Define study goals, design, and endpoints.
- Proposal & Quotation: Provide detailed protocol, budget, and timeline.
- Trial Execution: Manage sites, monitor data, and ensure patient safety.
- Data Reporting: Deliver clean datasets, interim updates, and final reports.
- Post-Project Support: Assist with regulatory queries and submission follow-ups.
Frequently Asked Questions (FAQs)
Q: Do you manage multi-country trials?
A: Yes — we have a global site network and regulatory liaison teams for multi-national trials.
Q: Can you handle patient recruitment for rare diseases?
A: Absolutely — we develop targeted strategies for rare and hard-to-reach populations.
Q: How secure is clinical trial data?
A: NDAs, encrypted systems, and GCP compliance ensure complete data confidentiality and integrity.
Get Started / Request a Quote
Contact us today to discuss your clinical trial requirements and receive a customized plan and budget aligned with your project timeline.
Contact Us
Email: research-outsourcing@nthrys.com
Phone: +91-8977624748
Contact Us