EDC Software for Clinical Trials in Singapore
HSA-aligned EDC for Singapore’s world-class clinical research ecosystem
Singapore sits at the centre of Asia-Pacific clinical research. Run clean, PDPA-conscious eCRF data through HSA-aligned workflows and DSRB-reviewed studies — priced in Singapore dollars.
- Compliant audit trails & e-signatures
- Local-currency pricing: S$1 to USD
- 14-day free trial, no credit card
- Deploy in days, not months
Singapore is a strategic hub for biotech and medtech trials, home to world-class academic medical centres and one of the most efficient regulatory pathways in Asia. The Health Sciences Authority (HSA) administers clinical trial notifications and approvals, while research in public healthcare institutions runs through Domain Specific Review Boards (DSRBs) and institutional review processes aligned to the national human biomedical research framework.
Trials in Singapore are often regional proof-of-concept studies that global sponsors expand into Southeast Asia. That places a premium on data quality and transparency from day one. Elysium Clinical Trials EDC gives sponsors, CROs and hospitals an eCRF environment that is immediately credible — audit-trail complete, GCP aligned and export-friendly.
This page covers the Singapore regulatory picture, how Elysium supports it, and what the platform costs in Singapore dollars.
Local Regulatory Authorities & Data Integrity
Elysium is engineered for the record-keeping expectations of the authorities that govern clinical research in Singapore.
HSA (Health Sciences Authority)
HSA administers clinical trial authorisation and notification in Singapore. Elysium supports the data-integrity and record-keeping expectations behind HSA trial authorisation.
DSRB & institutional review
Domain Specific Review Boards under the public healthcare clusters review human biomedical research. Versioned eCRFs and complete audit trails satisfy the documentation reviewers ask for.
PDPA (Personal Data Protection Act)
Singapore’s PDPA governs the collection, use and disclosure of personal data, including research contexts. RBAC, encryption, retention controls and access logging support PDPA obligations.
ICH GCP E6(R2)
The GCP standard expected by sponsors and CROs running Singapore-based studies; Elysium’s workflows align to it end to end.
Singapore’s research ecosystem moves fast and expects international-grade systems. Whether the study is a phase I proof-of-principle at a research hospital or a multi-country Southeast Asian programme anchored in Singapore, Elysium gives your team the same professional data infrastructure used in mature markets — without the licence and deployment overhead of legacy EDC.
A Complete Electronic Data Capture Platform
Everything your study team needs, from first CRF draft to database lock and export.
Drag-free eCRF Builder
Design case report forms with validation, skip logic and required-field rules — no code.
Study & Subject Management
Manage sites, visits, subjects and ePRO/pROM instruments from one workspace.
Security & Access Control
Role-based permissions, two-factor-ready logins, encryption in transit and at rest.
Queries & SDV
Raise, answer and close queries; schedule source-data-verification tasks for monitors.
Audit Trail
Every edit, signature and query is attributed, time-stamped and non-destructive.
Export & Reporting
Export to CSV, Excel, JSON or CDISC ODM; API access for downstream pipelines.
Electronic Signatures
e-sign at form, visit or study level with full linkage to the signer and timestamp.
Randomization
Coding and allocation management with support for commonly used randomization schemes.
Medical Coding
MedDRA/WHO-Drug-style term coding within the same environment you enter data.
From Sign-Up to First Data in Three Steps
Create an Account
Sign up for a 14-day free trial. No credit card, no procurement delay — your team can explore immediately.
Build Your CRFs
Model your study, sites and visits, then assemble eCRFs with the visual builder — most studies are live within a day.
Enroll & Monitor
Invite site staff, enroll subjects, run queries and SDV, then lock and export when your database is clean.
Built for how research teams in Singapore actually work
- Rapid setup for HSA notifications and DSRB-submitted protocols
- One platform for bilateral (Singapore + regional) and global studies
- Remote monitoring and SDV workflows for sponsors based anywhere
- Multi-language forms (English, Chinese, Malay, Tamil where required)
- High-volume data entry that keeps pace with fast-enrolling Singapore studies
- S$ pricing so local finance and grant budgeting is straightforward
Singapore intends to remain the region’s clinical research gateway, and competition between sites and CROs is strong. A modern, compliant data platform is now a differentiating factor in winning sponsor business. Elysium delivers that differentiation at a price point that makes sense in Singapore’s market.
Pricing for Singapore in Singapore Dollar
Transparent, local-currency figures so you can budget without doing the forex math. Billing on your invoice is in US dollars; equivalents are shown at the current rate.
Starter
For small studies and independent researchers
- 5 Studyies
- 50 Subjects
- 5 Users
- 2GB Storage
- Core EDC
- CSV Export and Import
- Audit Trail & Reports
- Internal Messaging System
- Query Management
Professional
For growing research teams and CROs
- 15 Studyies
- 500 Subjects
- 15 Users
- 5GB Storage
- REST API Access
- Core EDC
- CSV / Excel Export
- Audit Trail and Reports
- Internal Messaging System
- Query Management
Enterprise
For organizations running multiple concurrent studies
- 100 Studyies
- 5,000 Subjects
- 100 Users
- 25GB Storage
- REST API Access
- Core EDC
- All Exports / Import Options
- Audit Trail and Reports
- Query Management
- Priority Support
- Internal Messaging System
- Medical Coding (ATC/DDD, WHO ICD-10, LOINC)
- REST Api Access
- Desktop app (works offline as well)
Unlimited Plan
For large CROs and enterprise sponsors
- Unlimited Studyies
- Unlimited Subjects
- Unlimited Users
- 100GB Storage
- REST API Access
- All Advanced Features
- Dedicated Support
- Custom SLA
- Complete System Training
- Internal Messaging System
- Medical Coding (ATC/DDD, WHO ICD-10, LOINC)
- *Sensitive Medical Coding (medDRA and WHODrugs)
- REST API Access
- Desktop app (works offline as well)
Need a dedicated EDC built for your organization?
Custom study types, self-hosted or private-cloud deployment, local regulatory and language support, dedicated SLAs, SSO, and audit packs for Singapore-based sponsors and CROs.
Questions about EDC for Singapore
Does Elysium support HSA-authorised trials?
Yes. Elysium is designed for the data-integrity foundations behind HSA trial authorisation: audit trails, electronic signatures, versioned records and full export. Authorisation itself comes from HSA; Elysium covers the system your submission relies on.
How does Elysium fit DSRB review?
DSRBs evaluate how data will be handled, protected and reported. Elysium provides role-based access, complete audit history and transparent data flows, which strengthens the documentation you present to reviewers and supports continuing review.
Is Elysium PDPA-compliant?
Elysium supports the technical controls the PDPA expects — restricted access, encryption and audit logging — and processes data only as you instruct. Your organisation manages consent, purpose and retention; we can support a data protection impact assessment for your trial.
Can we expand a Singapore study to other Southeast Asian sites?
Yes. Build the study once, then add sites in Malaysia, Thailand, the Philippines or beyond under the same environment, applying site-level access rules. One audit trail covers the whole region.
What are the Singapore dollar prices?
This page shows SGD-equivalent figures for budgeting. Subscriptions are billed in US dollars with itemised invoices; see the pricing section for the current SGD numbers.
Elysium EDC in other regions
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