- 6th Floor, Pushparaj Circle, Sangli 416416
- Mon - Sat 10.00 - 18.00. Sunday CLOSED
Expert Clinical Trials
From Phase I to IV, we manage clinical trials with precision—handling patient recruitment, site selection, monitoring, and regulatory requirements.
Regulatory Excellence
We streamline regulatory approvals, ensuring compliance with drug/device submissions and ethics committee standards.
Training & Development
Our specialized GCP and regulatory training programs prepare professionals for excellence and compliance in clinical research.
Who We Are
Driving Innovation in Healthcare
Visshwa Solutions is a trusted Contract Research Organization (CRO) specializing in clinical trials, regulatory compliance, and medical research. We work with pharmaceutical, biotech, and healthcare companies to bring safe, effective treatments to market.
Our commitment to quality, ethics, and innovation ensures seamless clinical trial execution, regulatory approvals, and industry-leading training. Partner with us to advance healthcare together.
OUR SERVICES
Solutions That Deliver
Medical Writing
Expert medical writing services for protocols, CSRs, IBs, and regulatory documents with strict compliance to global guidelines.
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Clinical Trial
Comprehensive clinical trial management from protocol development to study completion, ensuring regulatory compliance.
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Clinical Trial Monitoring
Professional monitoring services ensuring data quality, protocol compliance, and patient safety throughout trials.
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Drug Safety Management
Comprehensive pharmacovigilance services including adverse event reporting, safety monitoring, and risk management.
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Clinical Data Management
Efficient data collection, cleaning, and analysis with advanced EDC systems and quality control processes.
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Biostatistics & Statistical Programming
Expert statistical analysis and programming services for clinical trials, ensuring accurate data interpretation and reporting.
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Quality Assurance & Compliance
Comprehensive quality assurance services including audits, SOP development, and regulatory compliance monitoring.
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Years of Experience
0Trials Completed
0Patients Recruited
0Experts Trained
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Our Testimonials
What Our Clients Say
Visshwa Solutions ensured seamless clinical trial execution. Their expertise in patient recruitment and compliance made a huge difference!
Their medical writing team delivered clear, precise study protocols, making regulatory approvals easy and hassle-free.
Navigating regulatory approvals was smooth with Visshwa Solutions. Their expertise truly saved us valuable time. From the beginning, they demonstrated a clear understanding of the process and guided us at every step.
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