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93% of clinical studies within our care are completed on or ahead of schedule and on budget

Successful Delivery of Clinical Trials From Start-Up to Close-Out

Our expert clinical operations team is integral to ensure the overall seamless execution of the study, ledgering their diverse skill set across planning, patient safety, quality and communication.

Our CRO services include:

  • Clinical trial feasibility assessment
  • Study start-up including site identification, qualification, and selection
  • Study document development
  • Essential document collection and maintenance
  • Translations
  • Trial master file set-up and maintenance
  • Site monitoring and management
  • Patient recruitment and retention strategies
  • Clinical trial management system
  • Training of clinical research associates
  • CRA management and quality control
  • Audit preparation
  • Regulatory & ethics committees submissions
  • Third-party vendor management
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25+

years experience in clinical research across all phases & indications

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93%

studies finished on time or ahead of time and on budget

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335000+

shipments to sites via our in-house clinical supply chain

Experience Across All Therapeutic Indications 

 

Our team has extensive experience and deep understanding of the latest advancements in all therapeutic areas  

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Oncology: 19.2%

Respiratory: 12.5%

Cardiology: 11.1%

Neurology: 10.4%

Metabolic: 8.4%

Gastroentology: 5.1%

Immunology & Virology: 4.7%

Infections: 4.7%

Gynaecology & Urology: 4.4%

Haematology: 4%

Rheumatology: 3.7%

Dermatology: 3.7%

Psychiatry: 3%

Pain management: 1.7%

Hepatology: 1%

Oto-rhino-laryngology: 1%

Neonatology: 0.7%

Orthopaedics: 0.7%

Highly Experienced and Trained Professionals 

SanaClis Clinical Research Professionals (CRAs) bring vast knowledge and experience to each clinical trial.

We pride ourselves in building and maintaining long-term relationships with clinical investigation sites. This approach allows SanaClis to achieve, and in most cases exceed recruitment targets in 93% of trials monitored and conducted within the company's portfolio of clinical studies.

 

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See how we’ve helped Protara Therapeutics to expedite timelines

By collaborating with SanaClis, Protara has been able to expedite timelines and maintain reliable and uninterrupted clinical supply and saw meaningful improvements in study activities after only 2 months of partnership.

Find Out More

Speak to an Expert

Reach out to our team of experts to discuss your project needs.

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