{"id":3073,"date":"2023-10-22T14:00:12","date_gmt":"2023-10-22T14:00:12","guid":{"rendered":"https:\/\/calian.stage.tbkdev.com\/dev\/calian.com\/src\/health\/?page_id=3073"},"modified":"2025-04-02T10:27:59","modified_gmt":"2025-04-02T14:27:59","slug":"contract-research-organization-services","status":"publish","type":"page","link":"https:\/\/calian.stage.tbkdev.com\/dev\/calian.com\/src\/health\/pharma-solutions\/contract-research-organization-services\/","title":{"rendered":"Contract Research Organization Services"},"content":{"rendered":"\n
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Contract research organization<\/p>

CRO services that inspire confidence <\/h1>

Full-service contract research organization (CRO) delivering excellence for more than 20 years. We have the knowledge and experience to help you achieve success in your product development programs. <\/p>

Request a quote<\/a>Download the brochure<\/a><\/div><\/div><\/div><\/div>\"A<\/div><\/div><\/div>\n\n\n\n
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Clinical study management<\/h3>
Study management is critical to the success of every project. Our experienced professionals deliver superior service by taking a collaborative approach to study management. This approach, combined with exceptional organizational and interpersonal skills, creates a responsive, client-driven environment.<\/p>\n

We manage each step of the process, from site selection and feasibility assessments to start-up, study planning, risk management and interaction with regulatory authorities and ethics committees.<\/div>

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Clinical monitoring<\/h3>
Our\u202fclinical research associates (CRAs) are known for their outstanding client service, attention to detail and in-depth knowledge of industry regulations and guidelines. They verify compliance with protocols, quality standards, data collection and regulatory guidelines\u2014ensuring the highest quality data for your clinical trial. <\/p>\n

We provide site selection, site initiation, interim monitoring and close-out visits, as well as remote monitoring, site personnel training, mentoring and guidance. We also assess protocol compliance and data integrity, as well as a host of other monitoring services.<\/div>

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Data management<\/h3>
We offer a full spectrum of data management services and expertise to optimize your data. Our clinical data managers rigorously follow standard operating procedures that encompass security, industry regulations and ICH\/GCP. They work collaboratively and cross-functionally to ensure all stakeholders’ needs are met. We use a comprehensive, but easy-to-use, cloud-based clinical data management platform that supports a wide range of study types and designs. <\/p>\n

From data management planning and CRF and database design to EDC database build and role-based security and access control, we have you covered.<\/div>

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Biostatistics<\/h3>
Biostatistical design and analysis are central elements of any clinical trial. Establishing a sound biostatistical plan results in optimal study design and high-quality data output. Comprehensive statistical input during the early stages of a clinical development program decreases overall costs and accelerates timelines to regulatory approval. <\/p>\n

We manage sample size calculation, protocol development support, statistical analysis plans, interim and final data analysis, support for medical writers and more.<\/div>

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Quality assurance<\/h3>
Our quality assurance team provides compliance oversight and guidance through carefully planned audits and detailed reports. This allows continuous process improvement to ensure the ongoing effectiveness of your clinical trial.<\/p>\n

We also offer quality assurance services that are independent audits of clinical investigational sites, processes, documentation and assessment of the quality of the data collected and processed.<\/div>

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End-to-end support for your clinical research<\/h2>

Calian has the knowledge and experience to support you at every stage of your clinical research and help you get your product approved.<\/p><\/div><\/div><\/div>

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