Validated CloudThe MUSA Validated Cloud
For more information, please visit our product website at www.validatedcloud.com.
At MUSA, we’ve leveraged years of validation, qualification and IT experience to create a Validated Cloud environment perfect for biotechnology, biomedical, and pharmaceutical companies. Our Validated Cloud is a private FDA-compliant cloud available on demand anywhere from any internet connection and designed specifically for the Life Sciences industry. Our Validated Cloud includes all of the features available from other industry sources and can be coupled with our Validation as a Service (VaaS) for additional 21 CFR compliance out of the box.
Validated Cloud is…
FDA 21 CFR Part 820/11 and GxP Documented – All of our standard system templates have been pre-approved by industry experts to provide operational and installation qualification documents that await your signature.
Open for Audits – All documentation is available for review by your internal auditors or by FDA inspectors.
Scalable – As your company grows and your data needs mature, the MUSA Validated Cloud scales to meet your dynamic storage and bandwidth requirements.
Available Globally – From your manufacturing room floor in London to your research laboratory in San Francisco, the same data, applications and configurations are available to all contributors globally (certain security encryptions are not available in all countries).
Quickly Deployed – Available in a quarter of the time of in-house validated deployments.
Affordable – Validated Cloud doesn’t require costly investments in hardware, software or the hiring of validation, compliance or IT professionals.
Customizable – Our packages are chosen à la carte so you can customize your Validated Cloud to fit your business needs. MUSA can deploy your cloud for your internal staff to manage and support or, for smaller companies, you can leverage our support staff to act as your information technology and quality assurance departments.
Secure – Your validated data is always secure and accessible via Virtual Private Network (VPN) or secured network data connection.
Available with Software as a Service (SaaS) – We’ll assist in the creation of URS, FRS, SDS, and Validation Plan documentation to support and validate the applications that you utilize in your day-to-day business.
Qualification Outsourcing with Validation as a Service (VaaS)
Validation is a necessity in the biotechnology, biomedical and pharmaceutical industries. For growing companies, qualification and compliance professionals can consume a significant portion of your budget that could be better invested in your core business. Validation as a Service (VaaS) gives you on-demand compliance for all of your validated documentation requirements - similar to having a department full of qualification experts on staff, but significantly more affordable. With VaaS, you leverage our consultants on an hourly basis according to your needs. MUSA’s specialists have experience in pharmaceutical and biomedical development as well as information technology and can create custom templates for everything including assay quality control through custom system resource and application configurations.
Team up your Validated Cloud with our Validation as a Service offering and let MUSA’s seasoned professionals handle all of your customized qualification-related information technology, manufacturing and research and development needs. Whether you leverage our existing Quality System or would like us to translate our documentation into your existing SOPs, our validation and compliance experts have the expertise to meet your dynamic needs. We’ll inspect and sign off on the final documentation to make certain that it meets FDA 21 CFR Part 820/11 requirements, giving you the confidence and peace of mind that you are in compliance with FDA regulations.
