MOALI CORP

Commissioning, Quality Management System, and Validation Services

MOALI corporation offers a wide range of validation and qualification techniques and services with the necessary tools and expertise to help grow your business. We partner with our clients from start to finish, focusing on their needs while producing new ideas, developing effective strategies and designing high quality and scaleable solutions. Contact us to learn more.

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About Us

Creative Solutions

MOALI corporation is an engineering and information technology solutions provider helping the pharmaceutical, healthcare, biotech, hospital, and medical device industries.
MOALI has been conducting utilities, facilities, equipment, process, test method, and computer system validations in the FDA regulated industries since 2009 at various client sites.
Though we’ve grown since our founding, we’re still the same agency at heart. Let us help make your dreams a reality. Are you ready to set your brand or business on the path to success? Give us a call today and see what we can do for you.

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Solutions

Discover Our Expertise

MOALI Corporation exists to solve the critical issues facing our clients, both large and small. Our unique approach is not only what differentiates us, but also what makes us successful. We provide a broad range of services and solutions to help organizations facilitate change, achieve their vision and optimize performance and productivity.
Project Management in Computer System Validation, Software Validation, Process Validation, Test Method Validation, Equipment/ Utilities/ Facilities/ Infrastructure Commissioning and Qualification, Analytical Laboratory Instruments Validation, Sterilization Process Validation, (Moist Heat, Dry Heat, Ethylene Oxide, Vaporized Hydrogen Peroxide, and Filtration), Lyophilization Process Validation, Aseptic Processing Technique Validation, Vial Washing Process Validation, Data Integrity Data Flow Mapping, Environmental Monitoring Systems, Controlled Environment Qualification, Manufacturing and Packaging Systems Validation, Validation and Verification, Periodic Process Validation Reviews, Periodic Computer System Validation Reviews, Validation Master Plans, Design History Files, Device Master Records, Design Controls, Change Controls, Deviations, Non-conformance, CAPAs, Remediation, Warning Letters, and Consent Decree Quality Management Systems.
FDA regulated industries (pharmaceutical, healthcare, biotech, hospital, and medical device)
cGXPs (cGMP, cGLP, and cGCP)
21 CFR Part 4, 11, 210, 211, 803, & 820
ISO 13485, 14644, 14971, 9001, 11135, and 11137
EU GMP Annex 11, JP 11, Health Canada, Australia, and Taiwan FDA
ICH Q7, Q8, Q9, and Q10
GAMP 5