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AltaQ offers a full range of validation services to medical device, pharmaceutical, and biotechnology companies from planning through execution and final reporting. This includes validation activities covering product, process, system, equipment, facility and more. 


Experts at AltaQ use regulatory knowledge and best practices to optimize validation planning, and execution to save our clients time and money. AltaQ assembles focused project teams to assist with processes such as validation master planning, protocol development, project administration, execution activities, final reporting, and documentation. 


Our team has successfully completed projects in the US, Europe, China, Japan, and South Asia. We would like to meet with you to provide a free compliance summary assessment regarding your validation needs. Click Here. 

AltaQ has the capability and expertise to provide complete validation services in the following areas:

  • Validation Master Planning

  • Process Validation

  • Facility Qualification

  • Utilities Qualification

  • Equipment Qualification

  • Cleaning Validation

  • Sterilization System Validation

  • Filing and Packaging Equipment Qualification

AltaQ has the expertise to provide software and computer system validations covering:

  • Software System (Process and Products)

  • 21CFR Part 11 Compliance

  • ERP and MRP System

  • Document Management Systems

  • CAPA Systems

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