Our Services

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At Veroaks Therapeutics, we understand that successful clinical trials require more than just good science – they require efficient and effective clinical operations management. That's why we offer a full range of clinical operations services to help our clients confidently plan, execute, and manage their clinical trials.

Our experienced team of clinical operations professionals have a deep understanding of the regulatory environment, industry best practices, and the unique challenges of clinical research. We are committed to providing customized solutions tailored to each client's specific needs while maintaining the highest standards of quality, accuracy, and integrity.

Our Services Include: 

• Protocol development: We can help design and develop a clinical trial protocol that meets regulatory requirements and scientific objectives.
• Site selection and management: We can assist with site identification, selection, and initiation and provide ongoing site management and support throughout the trial.
• Patient recruitment and retention: We can help design and implement patient recruitment and retention strategies to ensure enrollment targets are met and patients remain engaged in the trial.
• Study monitoring: We can provide on-site and remote monitoring to ensure that the trial complies with protocol requirements, regulatory requirements, and GCP standards.
• Data management and analysis: We can provide data management and analysis services, including database design and management, data cleaning, statistical analysis, and report generation.
• Medical writing and regulatory submissions: We can provide medical writing services, including protocol writing, clinical study reports, and regulatory submissions, to help ensure that all documents are of the highest quality and meet regulatory requirements.

At Veroaks Therapeutics, we understand that clinical monitoring is a critical component of successful clinical trials. That's why we offer a full range of clinical monitoring services to help our clients ensure that their trials comply with protocol requirements, regulatory requirements, and GCP standards.

Our team of experienced clinical monitors is dedicated to providing customized solutions tailored to each client's specific needs while maintaining the highest quality, accuracy, and integrity standards. We use a risk-based approach to monitoring, focusing on the areas of highest risk to ensure that the trial data is of the highest quality and is conducted safely and ethically.

Our clinical monitoring services include the following:

• Site selection and initiation: We can help identify and select appropriate clinical trial sites and provide on-site initiation visits to ensure that the site is prepared to conduct the trial.
• On-site monitoring: We can provide on-site monitoring visits to ensure that the trial complies with protocol requirements, regulatory requirements, and GCP standards.
• Remote monitoring: We can provide remote monitoring services to supplement on-site monitoring, including a review of electronic data capture (EDC) systems, a review of source documents, and a review of other trial documentation.
• Site management: We can provide ongoing site management and support throughout the trial, including resolving issues and ensuring the site fully complies with regulatory requirements.
• Training and support: We can provide training and support to clinical trial site personnel to ensure they are fully prepared to conduct the trial and comply with all relevant requirements.

At Veroaks Therapeutics, we understand that effective site management is essential for successful clinical trials. That's why we offer a comprehensive range of site management services to help our clients ensure that their clinical trials comply with regulatory requirements and GCP standards and that data is of the highest quality.

Our experienced site managers are dedicated to providing customized solutions tailored to each client's specific needs while maintaining the highest standards of quality, accuracy, and integrity. We work closely with clinical trial sites to ensure that the are fully prepared to conduct the trial and comply with all relevant requirements.

Our site management services include the following:

• Site identification and selection: We can help identify and select appropriate clinical trial sites based on the specific needs of each trial.
• Site initiation: We can provide on-site initiation visits to ensure the site is fully prepared to conduct the trial and comply with all relevant requirements.
• Site monitoring: We can provide ongoing site monitoring to ensure that the trial complies with protocol requirements, regulatory requirements, and GCP standards.
• Site closeout: We can provide site closeout services to ensure that all site trial-related activities are completed promptly and efficiently.
• Investigator and site staff training: We can provide investigator and site staff training to ensure that all personnel is fully prepared to conduct the trial and comply with all relevant requirements.
• Patient recruitment and retention: We can help design and implement patient recruitment and retention strategies to ensure enrollment targets are met and patients remain engaged in the trial.

Veroaks Therapeutics is dedicated to providing high-quality regulatory services for clinical research studies, helping our clients to navigate the complex and constantly evolving landscape of regulatory requirements. Our experienced professionals are committed to delivering customized solutions tailored to each client's specific needs while maintaining the highest standards of accuracy, integrity, and confidentiality. 

Our services include:

• Study design and planning: We can provide expert guidance on study design and protocol development, helping to ensure that your research meets all relevant regulatory requirements and ethical standards.
• Regulatory submissions: We can prepare and submit regulatory documents to regulatory agencies, including investigational new drug (IND) applications, new drug applications (NDAs), and biologics license applications (BLAs).
• Compliance support: We can help ensure that your study is conducted in compliance with applicable regulations and guidelines, including the International Conference on Harmonization (ICH) guidelines, Good Clinical Practice (GCP) standards, and the Code of Federal Regulations (CFR).
• Clinical trial management: We can support the entire process, including site selection, monitoring, data management, and safety reporting.
• Post-marketing support: We can provide ongoing support after regulatory approval, including post-marketing surveillance, safety reporting, and compliance with post-marketing requirements.