TRANSFORMNG HEALTH CARE, ONE TRAIL AT A TIME
Magnadyne Solutions is a global CLINICAL RESEARCH ORGANIAZTION — built for sponsors and Pharma Stakeholders who demand zero compromise on trial integrity, uncompromised data, regulatory confidence, speed to lock and submission ready.
97+
Clinical Trials Delivered (Phase I–IV) In the last 24 Months
1,200+
Patients Enrolled Across Global Studies
98%
On-Time Database Lock
96%
Client Retention Rate
8+
Countries Across Active Trial Delivery
Full-Spectrum Clinical
Trial Management.
GASTROENTEROLOGY & IBD
ONCOLOGY & HAEMATOLOGY
Phase I–III oncology trial management with biomarker strategy, imaging oversight, safety monitoring, medical data review, and complex operational delivery across global sites.
IMMUNOLOGY & RHEUMATOLOGY
Integrated autoimmune trial delivery including biomarker operations, patient monitoring, laboratory coordination, regulatory support, and longitudinal endpoint management across multi site studies.
RARE & ORPHAN DISEASE
CARDIOVASCULAR & METABOLIC
NEUROSCIENCE & CNS
Full-service CNS trial delivery with cognitive assessment oversight, ePRO integration, patient
engagement strategies, and longitudinal study management for complex neurological indications.
We work in your
system. Natively.
We hold active certified partnerships across multiple leading eClinical EDC platforms. No system migration, no re-platforming — we embed directly into your existing infrastructure and deliver our expertise from day one.
Medidata Rave
Strategic Alliance
Zelta
Certified Partner
Medrio
Premium Partner
Clinion
Certified Partner
Clinspark
Alliance Partner
Veeva Vault
Collaborative
Wumedoo
Integration Partner
From first patient to
database lock.
01
Study Conduct Takeover
Mid-study transitions executed with a structured 72-hour gap analysis, dedicated DML assignment, and parallel-run protocol — zero disruption to timelines or data integrity.
Gap Analysis
Parallel Run
Zero Disruption
02
Database Design & Build
UAT
eCRF Build
CDASH
21 CFR Pt 11
03
Data Cleaning & Query Management
MedDRA
WHODrug
SLA-Driven
04
Closeout & Database Lock
Database Lock
DMR
Archival
Annex 11
Performance Benchmarks — CDM Delivery
Performance Benchmarks — CDM Delivery
72h
Gap Analysis
2 Wks
10d
Live
Numbers that speak
for
themselves.
“Magnadyne didn’t just support our study operations, they became a strategic extension of our clinicalteam, driving execution, oversight, and delivery across six concurrent oncology trials.”
Integrated CRO Partnership
We operate as a seamless extension of your clinical organization, aligning strategy, operations, oversight, and execution across the full trial lifecycle.
Accelerated Study Start Up
From protocol handoff to study activation, our teams mobilize rapidly with dedicated clinical, regulatory, and operational leadership in place.
Inspection Ready Operations
Across global studies and regulatory engagements, we maintain rigorous quality oversight, GCP aligned processes, and inspection ready trial execution.
Ready to elevate
your clinical trial delivery?
Let’s build a strategic partnership that accelerates study execution, strengthens regulatory confidence,
and advances your clinical Programme from start up to close out.
