In a dynamic and often challenging regulatory environment, we help companies navigate through the maze and achieve their goals by our suite of products, managed services, strategic consulting, and staffing services. Each organization is different with the unique challenges and ecosystem that it operates in. We collaborate with you to build innovative solutions that are robust, yet flexible and achieve the desired outcomes.
Companies that automate and integrate their laboratories, manufacturing, quality, ERP, regulatory, and compliance domains can effectively control costs, reduce bench to market time for their products, improve quality and gain meaningful insights through data intelligence. If you are a start-up or already established, we can help in your journey to automate and integrate different business areas.
Our implementations of fully validated solutions like Electronic Lab Notebooks (ELN), Laboratory Information Management Systems (LIMS), Chromatography Acquisition systems, Document Management Systems (DMS) have helped numerous clients with the reduction in testing life cycle times, lower inventory overheads, improved data integrity, compliance with 21CFR Part 11 and GMP regulations and effective data analysis and reporting.
Riva professionals have expertise in implementing and managing numerous off-the-shelf products available in the market. Speak to us, we can assist you with products assessment, selection, and partner with the selected vendor throughout the implementation process.
At times the unique needs of a business require software applications that are not readily available. We cater to such needs with our in-house Product Development and Engineering group. We build custom applications, data intelligence, reporting solutions, APIs, and many more based on customer requirements. The delivery model offered by Riva Scientific ensures the developed product is of the highest quality, scalable, meets business requirements, delivered on time with available post-deployment support and maintenance.
Software validation and equipment qualification are critical components for Pharmaceuticals and Biotech companies to ensure their products meet quality, safety, and regulatory requirements in the markets they operate.
The validation and testing services offered by Riva Scientific allow companies to validate new and existing systems using either our fully on-site, offshore or hybrid model that meets a client’s time and budget constraints. Our professionals bring decades of experience in performing computer systems validation (CSV), manual & automated testing, GxP & 21 CFR Part 11 Assessments, compliance gap assessment, remediation strategies, drafting various technical documents, and many more.
Augment your team with Riva professionals or let us take care of the entire validation and testing effort. Contact us today. We would be glad to discuss your specific needs and customize a package that meets your time and budget.
The right professional is always a difficult find! It's an onerous task to locate individuals with the skill set, aptitude, and talent that are a good match for the team and company's ethos. Our network of recruiters with an eye for top talent removes the guesswork and can make staff augmentation stress-free. Contact us today for your staffing needs for full-time and contract openings.
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