Home/Research Capabilities
Infrastructure & Operations

Built to run your protocol end to end.

From patient identification through sample processing and cold-chain storage, our on-site capabilities are structured to protect data quality, participant safety and your timelines.

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Examination rooms, plus 2 offices
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Highest-recruiting site globally in the Bayer SEAFRONT cardiovascular trial
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Patients in a pre-screenable EMR database
I–IV
Clinical research phases supported
Site Facilities & Operations

The practical details sponsors ask about.

Space, systems and contingencies in place to support monitoring visits, protocol visits and continuous study conduct.

Examination rooms & offices

Six examination rooms and two offices for study visits, consent discussions and assessments.

Dedicated monitoring workspace

A private workspace for sponsor and CRO monitors during on-site visits.

Remote monitoring capability

Support for remote and hybrid monitoring alongside on-site visits.

Secure internet & document access

Reliable internet with secure, access-controlled arrangements for study documents and records.

Temperature monitoring & excursion alerts

Continuous temperature monitoring of storage units, with excursion notification to site staff.

Backup power plan Being added

A documented backup power plan protects stored product and samples; a backup generator is being installed.

Weekend & extended hours

Weekend and extended-hour availability to accommodate protocol visit windows and participant schedules.

Nearby emergency & hospital access

Close to Windsor Regional Hospital — Metropolitan Campus for emergency care and hospital services.

EDC & systems experience

Hands-on experience with Castor EDC and LabView360, alongside electronic medical records.

Access controls

Restricted access to investigational product, study files and research areas.

Patient Access & Recruitment

Reach eligible participants — quickly.

A large, active primary-care population and established referral networks let us pre-screen and enrol with speed.

EMR database of 2,000+ patients

An active electronic medical record population enabling electronic pre-screening and targeted, protocol-specific patient identification.

Electronic pre-screening

Structured database queries surface eligible candidates against inclusion and exclusion criteria before outreach begins.

Cardiology referral network

Established referral relationships with the Windsor Cardiac Centre and Windsor Heart Institute broaden the cardiology recruitment pool.

Stroke clinic referrals

Access to stroke-clinic referrals through Windsor Regional Hospital supports neurology and cardiovascular programs.

Clinical & Diagnostic Equipment

On-site diagnostics reduce external dependencies.

Electrocardiography (ECG)

12-lead ECG for cardiovascular assessment and safety monitoring.

Holter Monitoring

Ambulatory cardiac monitoring for extended rhythm assessment.

Automated Calibrated BP Monitoring

Standardized blood-pressure measurement for protocol compliance.

Echocardiogram & Stress Testing

Access to echocardiography and stress testing for cardiac studies.

Centrifuge & Sample Processing

On-site centrifuge for timely, compliant biological-sample handling.

Lab, X-ray, Ultrasound & Pharmacy

Laboratory access, X-ray, ultrasound and pharmacy — all in-building.

Investigational Product & Sample Storage

A monitored, secure cold chain.

Temperature-controlled storage with continuous monitoring and excursion notification, backed by a backup power plan, safeguards investigational product and biological samples across the full cold-chain range.

−86 °CUltra-low freezer with continuous alarm monitoring
−20 °CFreezer for sample storage Being added
2–8 °CMonitored refrigeration for IP and samples
24/7Temperature monitoring with excursion notification

Secure IP & drug storage

Controlled-access storage of investigational product with documented chain-of-custody and temperature records.

Storage & monitoring · photo
Research Operations

Disciplined execution, from SOPs to sign-off.

Trained staff and defined processes keep studies compliant, efficient and audit-ready.

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GCP & IATA-trained staff

Research team trained in ICH Good Clinical Practice and IATA dangerous-goods regulations.

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Electronic medical records

EMR-driven workflows underpin pre-screening, scheduling and source documentation.

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Rapid study start-up

Streamlined activation shortens the path from site selection to first patient enrolled.

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Retention strategies

Patient-centred coordination sustains engagement through study completion.

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Quality data collection

A commitment to clean, complete, verifiable data and regulatory compliance.

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Dedicated research team

Two physician assistants, a registered practical nurse, a medical technologist and research coordinator, and a phlebotomist supporting the Principal Investigator.

Need our full equipment inventory?

We can provide a detailed capability statement and equipment list to support your feasibility assessment.