Technology implementation services

Enhance every stage of your clinical development with our comprehensive technology implementation, integration, and migration solutions. From seamless initial implementation to ongoing support, we streamline the management of drug safety and development data. By leveraging data-driven insights, we accelerate trials and improve outcomes, helping you navigate the complexities of clinical development thru commercialization more efficiently and effectively.

Maximize efficiency with integrated technology solutions

Our end-to-end technology services include system implementation, upgrades, and validation. With a hybrid delivery model that reduces costs and speeds up rollouts, we provide expert advisory, training, and analytics to help you achieve your business and compliance goals. Discover how our solutions enhance clinical development through the use cases below.

Full-service pharmacovigilance as a service (PVaaS) integrating cutting-edge AI & advanced analytics technology for compliance, safety, and efficiency

End-to-end case intake, processing, and aggregate reporting for seamless drug safety management
Signal detection, safety risk management, and Qualified Person Responsible for Pharmacovigilance (QPPV) support to maintain global regulatory compliance
Real-time analytics and data visualization to optimize safety decision-making
Continuous adaptation to new regulatory requirements and industry standards

Tailored technology services that streamline business processes and improve system functionality

Comprehensive system implementation for optimal alignment with business, technical, and functional requirements
Efficient data migration and system integration using industry-standard formats and third-party tools
Seamless updates to drug safety systems, ensuring access to new features and improvements
Script development and validation to meet business requirements and ensure successful project execution

Leverage advanced AI-driven technology to integrate systems, enhance business intelligence (BI) and provide ongoing support

BI capabilities powered by generative AI for enhanced data visualization, safety reporting, and drug discovery insights
Seamless system integration (e.g., PVA with Argus) to meet specific business functionality
Comprehensive end-user support post-implementation, with expert troubleshooting for third-party technologies
Creation of a structured database to track and resolve recurring technical issues efficiently

Expert guidance to drive your success with strategic problem-solving and regulatory intelligence solutions

Regulatory intelligence automation to track global regulatory changes and ensure compliance effortlessly
Strategy, planning, and problem-solving to optimize business processes and enhance operational efficiency
Rigorous application change management, ensuring proper procedures for updates, hot fixes, and patches
Coordination with vendors to resolve challenges and maintain system integrity throughout the project lifecycle

why synapmed?

Synapmed offers cutting-edge AI, intelligent automation and workflow, and advanced analytics technology solutions to optimize every phase of your clinical development and commercialization.

Our comprehensive approach integrates pharmacovigilance as a service (PVaaS), system implementation, and business advisory services to streamline drug safety and data management. From initial setup to ongoing support, we leverage data-driven insights to accelerate trials, ensure compliance, and improve outcomes.

Our expert advisory and efficient project delivery services help reduce costs, enhance compliance, and meet your business goals with ease.

Frequently asked questions

What are technology implementation and integration services?

Technology implementation and integration services involve deploying and linking various systems to streamline business processes. This includes setting up new technologies, integrating them with existing systems, and ensuring they work together efficiently to meet operational needs across all service areas, including pharmacovigilance and business advisory services.

How do technology implementation services benefit the clinical development process?

Technology implementation services optimize the setup of systems and tools, enhancing data management and regulatory compliance. By providing a cohesive and integrated solution for managing clinical data, these services reduce time and costs, accelerate trials, and improve outcomes.

What is included in system implementation and upgrade services?

System implementation and upgrade services cover deploying new systems, updating existing ones, and integrating them with other technologies. This includes configuring systems to meet specific needs, enhancing features, and ensuring that upgrades are seamless and non-disruptive.

How does technology integration support business goals?

Technology integration ensures that various systems and applications work together smoothly, facilitating efficient data flow and process automation. This alignment supports business goals by improving operational efficiency, reducing errors, and enhancing the overall quality of clinical development activities.

What kind of support is available after system implementation?

Post-implementation support includes troubleshooting, user assistance, and maintenance. This ensures that any issues are promptly resolved and systems continue operating effectively and efficiently.

Can you assist with data migration during technology implementation?

Our technology implementation services include data migration, which involves transferring data between systems using standard formats or third-party tools. This ensures secure and accurate data transfer, minimizing disruptions during the integration of pharmacovigilance and business intelligence systems.

What is involved in the validation process for new systems?

Validation includes developing and executing scripts to ensure that the new system meets all business requirements. This process confirms that the system functions correctly and complies with regulatory standards, including those specific to pharmacovigilance and safety reporting.

How do technology implementation services ensure regulatory compliance?

Technology implementation services are designed to meet industry standards and regulatory requirements. Comprehensive validation and ongoing support ensure your systems maintain compliance throughout their lifecycle, particularly in pharmacovigilance as a service (PVaaS).

How does Synapmed handle regulatory compliance in technology implementation?

Synapmed’s technology implementation services are tailored to meet regulatory requirements. We focus on ensuring compliance through thorough validation and support, helping you navigate regulatory standards effectively.

What expertise does Synapmed offer in technology advisory, project delivery and change management?

Synapmed provides strategic technology advisory, project delivery and change management services, offering guidance on planning, problem-solving, and implementing changes. Our expertise ensures that new technologies align with your business objectives and regulatory requirements, optimizing your technology investments.

How does Synapmed’s pharmacovigilance service integrate with technology implementation?

Our pharmacovigilance as a service (PVaaS) offerings integrate seamlessly with technology implementation to ensure that case intake, processing, and reporting systems fully align with your operational needs. This integration allows for efficient safety data management and compliance with regulatory standards.

What role does business intelligence play in Synapmed's services?

Our business intelligence advisory services leverage generative AI technology to enhance drug discovery, optimize safety data management, and provide insightful data visualization. This empowers your organization to identify gaps and opportunities, ultimately supporting better decision-making in clinical development.

How can Synapmed help with regulatory intelligence?

Synapmed’s regulatory intelligence services provide a unified solution for monitoring global regulatory changes. By automating these services, we help your organization stay compliant while eliminating the hassle of manually tracking various sources of regulatory information.

“Synapmed allows us to build expertise within our company while also outsourcing the administrative aspects. When you work with most vendors, it becomes an assembly line, and quality goes down. Or they take over completely, and we lose oversight. Synapmed is a part of my team, so we get to maintain and retain the quality.” 

“I build and fix departments and Synapmed has been part of that journey with me. We wanted to come up with a safety profile for one of our drugs. Because of the performance of competitor generics, it was getting a bad name. Synapmed mined the data, analyzed our product versus generics from a safety perspective, and wrote an article and abstract on the findings that was very productive.”

What is the Right Outsourcing Strategy for Your Company? Not One Model Fits All

Pharmacovigilance (PV) is crucial for the pharmaceutical and biotech industries as safety regulations grow increasingly complex. Companies encounter challenges in managing rising data volumes, resulting in higher costs and a need for specialized expertise. In response, many organizations are outsourcing PV functions to cut costs and tap into expert knowledge. Successful outsourcing hinges on careful partner selection aligned with specific needs, while retaining essential tasks in-housed when necessary. By effectively managing these partnerships, companies can navigate the complexities of pharmacovigilance while concentrating on their core competencies.

Dedicated to youR Project

No matter the size or scope of your projects, you have a committed partnership team with Synapmed. A team that listens, pays attention to details, and brings smart insights to the table. All so you can solve real problems throughout the product development and commercialization lifecycle.

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