Improve your Performance in the Hospital and Health Systems Marketplace
PruTech's experienced consultants work seamlessly with clients in the pharmaceutical, biotechnology, and medical device/diagnostic industries to resolve complex problems, implement the best practices, and continuously improve operational processes at critical junctures. We have tailored our services to assist our clients in meeting strategic business goals as well as in complying with regulatory standards.
PruTech provides a full range of clinical services and resources to ensure expedited development and successful submission to regulatory agencies. We offer services ranging from single components, such as monitoring and data management, to fully integrated clinical development programs.
Our expert staff design, develop, and maintain quality systems and ensure the validity and accuracy of required data. PruTech also assist clients in complying with FDA regulations and guidelines.
ERP Supplier and Customer Integration
Supply chains need to be effectively managed for your customers as well as your suppliers. Organizations need to have an integration strategy that creates better forecasting of their customer needs and keeping supply resources available to meet this demand. PruTech Solutions can implement ERP Supplier and Customer Integration platform that provides documented and uniform interfaces that can be easily adapted and maintained by our clients.
Business Intelligence (BI) systems are implemented to provide current, historical, and future views of business information. The standard process is to collect information into data warehouse or data mart for an aggregate view of specific business operations such as sales, production, financial and many other sources. BI Software elements support reporting, interactive analyses, dashboards and statistical data mining. PruTech can assist clients improving their existing data warehouse applications, integrate with new data sources and provide robust search and filtering tools to present data in easily accessible components.
Compliance requirements are affecting all types of businesses and organizations today. Many companies have specialized processes that are needed to meet industry specific regulations. As these state and federal regulations continue to grow, many of these compliance criteria can become more intertwined and can lead to duplicate and sometimes contradictory documentation and procedures. Implementing a system that organizes the regulatory procedures can reduce potential risks, increase efficiency of meeting compliance profiles and decrease the cost of manage multiple regulatory needs.
Below are additional solutions we provide to our pharmaceutical clients:
- Case report form design and production
- Database and data entry screen design
- Adverse event and medication coding (MedDRA, WHO DRUG, client-customized dictionaries)
- SAE reconciliation
Computer System Validations
- Document management
- Quality Assurance
- Technical writing
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Contact us for a free consultation for all your IT solutions needs.
Call: (732) 404 1600
555 U.S. Highway 1 South
Iselin, New Jersey 08830
(732) 404 1600
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Charlotte, North Carolina 28202
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New York City, New York 10007
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