Crystal Life Sciences provides comprehensive clinical research, regulatory affairs, pharmacovigilance, medical writing and data management solutions to pharmaceutical, biotechnology and healthcare organizations.
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Delivering reliable, compliant and sponsor-focused clinical research solutions since 2010.
Providing outsourced pharmaceutical research and clinical support services to pharmaceutical, biotechnology and healthcare industries.
Delivering efficient, high-quality research solutions tailored to sponsor requirements.
Supporting projects from full-service clinical research to specialized niche services.
Committed to the highest standards of quality, compliance and professionalism.
Protocol development, site selection, monitoring, recruitment, data management and medical writing.
Comprehensive clinical research and site management solutions supporting sponsors, CROs, pharmaceutical and biotechnology organizations.
Cost assessment, budgeting, timelines, patient recruitment planning and complete study lifecycle management.
Patient recruitment, site coordination, CRF management, EC submissions and protocol compliance support.
Investigator evaluation, patient population assessment, site qualification and feasibility studies.
ICH-GCP, protocol-specific training, SAE reporting, EDC systems and site staff education.
SOP compliance, audits, CAPA management and quality systems oversight.
Clinical documentation, coordinator support, EDC management and regulatory readiness.
Crystal Life Sciences has successfully completed clinical trial and clinical data management projects across multiple therapeutic areas.
Multicentric, double-blind, placebo-controlled clinical trial.
Piramal Life SciencesClinical trial in CKD patients with anemia on dialysis.
Emcure PharmaceuticalsOphthalmology clinical study for treatment of Dry Eye disease.
Ajanta PharmaFull-service CRO project including trial coordination, CDM and final report.
Tosk Inc., USAClinical trial in newly diagnosed, treatment-naïve patients.
Piramal Life SciencesClinical data management project with final report submission.
RA Chem PharmaClinical trial in Chronic Kidney Disease patients not on dialysis.
Cadila HealthcareClinical trial in Chronic Kidney Disease patients on dialysis.
Cadila HealthcareDelivering quality, compliance and reliability throughout the clinical research lifecycle.
Over a decade of experience providing clinical research, site management and regulatory support services.
Comprehensive outsourced clinical research services tailored to sponsor and project requirements.
Access to research sites across Pune, Mumbai, Chennai, Kolkata, Nagpur and other major cities.
Experience in Ophthalmology, Oncology, Dermatology, Cardiovascular, Respiratory and other therapeutic areas.
Strong focus on ICH-GCP compliance, protocol adherence and regulatory excellence.
Commitment to data integrity, patient safety, quality assurance and operational excellence.
Extensive experience across diverse therapeutic areas supporting clinical development programs.
Committed to regulatory excellence, quality systems and ethical clinical research practices.
Adherence to International Council for Harmonisation Good Clinical Practice guidelines.
Experience with EC submissions, approvals and ongoing compliance requirements.
Support for CDSCO, DCGI and other applicable regulatory requirements.
Focus on protocol compliance, documentation quality and data integrity.
Trusted clinical research support since 2010
Experience supporting clinical research programs.
Experience across multiple therapeutic areas.
Committed to quality, compliance and client satisfaction.
Comprehensive CRO, clinical research and regulatory support services.
Crystal Life Sciences provides end-to-end clinical research, site management, regulatory affairs, pharmacovigilance and medical writing support tailored to sponsor and project requirements.
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