Soterius

Name: Soterius
Address: 5 Independence Way, STE# 300, Princeton, NJ, 08540, US
Telephone: +12122030450

We are Soterius – a strong team of experienced professionals from the pharma industry.

We design customized, innovative, and cost-efficient processes for clinical safety, pharmacovigilance, and medical affairs. Our deep industry knowledge and up to date insights let us combine agile, people-powered intelligence with big data in pioneering customer-centric solutions.

04/03/2024

Discover the nuances of multilingual intake, local literature search, and local PV responsible/safety officer implementation with our expert-led webinar on: EU PV Optimization: Streamlined Technology Driven Oversight & Unified Governance

Don’t miss out! Register now @ https://bit.ly/Webinar-EuPv

04/02/2024

We’re excited to share that another U.S based Clinical Study Site has been trained on our innovative Safety Document Notification system, UNITYdx™: A Revolution in Clinical Trials

Reach out to us today for a demonstration at [email protected] or visit https://bit.ly/UNITYdx to learn more about UNITYdx™

04/01/2024

Join Dr. Sumit Verma and Dr. Parul Singla for a Live Webinar on 4th April. Our experts will dive into the intricacies of EU PV Optimization and elevate your understanding of streamlined governance.

Don't miss out on this opportunity to gain essential knowledge and optimize your EU PV practices! Reserve your spot now: https://bit.ly/Webinar-EuPv

03/26/2024

Join us for our upcoming webinar focused on “EU PV Optimization: Streamlined Technology Driven Oversight & Unified Governance” on 4th April.

Get Expert Insights on:
• Comprehensive Understanding of Local Responsible Person (LRP) Requirements.
• Importance of local literature searches in pharmacovigilance within the EU.
• Practical strategies for handling the complexities of multi-language adverse event.
• Methods for seamless integration with the central QPPV office.

Register @ https://bit.ly/Webinar-EuPv

03/20/2024

Dive into the intricacies of EU PV Optimization and elevate your understanding of streamlined governance and cutting-edge technologies with our expert-led session on 4th April.

Register @ https://bit.ly/Webinar-EuPv

03/18/2024

We're thrilled to announce that another Clinical Study Site has successfully completed training on our cutting-edge Safety Document Notification system, UNITYdx™

Reach out to us today for a demonstration at [email protected] or visit https://bit.ly/UNITYdx to learn more about UNITYdx™

03/13/2024

Join our experts Dr. Sumit Verma and Dr. Parul Singla for an in-depth exploration of EU PV Optimization: Streamlined Technology Driven Oversight & Unified Governance on 4th April.

Key takeaways:
• Comprehensive Understanding of Local Responsible Person (LRP) Requirements: Participants will gain insights into the landscape of LRP requirements in the EU.
• Importance of local literature searches in pharmacovigilance within the EU.
• Practical strategies for handling the complexities of multi-language adverse event (AE), product quality complaints (PQC), and medical information intake for drugs and devices in the EU.
• Explore methods for seamless integration with the central QPPV office, emphasizing on centralized operations management and governance, along with leveraging technologies to optimize overall pharmacovigilance processes.

Don't miss this opportunity to gain valuable knowledge and optimize your EU PV practices. Register @ https://bit.ly/Webinar-EuPv

03/08/2024

Happy International Women's Day to all the incredible women out there! Your strength, resilience, and achievements inspire us every day.

Let’s emphasize the importance of , and the crucial role of in achieving . It calls for action to break down barriers, challenge , and create environments where all women are valued and respected.

Together we can forge women's equality. Collectively we can all .

03/05/2024

Attention clinical trial professionals! Register for our webinar and explore the power of UNITYdx™ in simplifying safety document distribution. Say goodbye to manual processes and hello to efficiency.

Don't miss out; register now: https://bit.ly/Webinar-SUSAR

Key takeaways:
1. Regulatory Requirements for reporting of 7/15-day SUSARs to Clinical Sites for Clinical Trials in the US/EU
2. Emphasise the critical need for sponsors to transition from manual approaches in managing compliance for SUSAR reporting in multi-centric studies to more efficient and automated solutions, ensuring streamlined coordination, enhanced documentation practices, and reduced risks of non-compliance and audit discrepancies.
3. Streamlining of multi-country trials with automated reporting rules, ensuring seamless compliance management and reducing the complexity associated with diverse regulatory requirements across different regions
4. Ensuring data security with robust measures to protect sensitive information related to SUSAR notifications

03/04/2024

With our latest release of UNITYai.Lit™, we are able to import into any safety database E2B R3 files for ICSRs that include the Full Text Publication for an ICSR, such that you save on the overall cost of processing a literature article, along with saving valuable time in re-processing a literature article, looking for and purchasing the full text, analyzing and processing it.

UNITYai.Lit™ also allows you to configure desired categories for literature assessment, and review samples of your literature outputs on a periodic frequency. The in-built Workflow Scheduler gives you the required sample for review, on the day of the week/month that you desire, replete with auto-assignment and workflow management capabilities.
Reach out to us today for a demonstration at [email protected] or visit https://bit.ly/UNITYaiLit to learn more about UNITYai.Lit™

02/29/2024

Did you know? Millions around the world face the challenges of rare diseases every day.

Small steps, big impact. Join the fight against rare diseases on this World Rare Disease Day.

02/28/2024

Are you tired of manual processes for safety document management? Join our webinar 👉🏻 https://bit.ly/Webinar-SUSAR and discover how UNITYdx™ automates safety document distribution, improves compliance tracking, and enhances efficiency.

Register today and embrace the future of clinical trials!

Address

5 Independence Way, STE# 300
Princeton, NJ
08540

Telephone

+12122030450

Website

http://www.soterius.com/

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