Expertise in Validation Documentation and Execution Services
At Valqpro LLP, we provide complete Validation Documentation and Execution Services tailored for pharmaceutical, biotech, food, and healthcare facilities. Our team prepares and executes validation protocols in accordance with GMP, WHO, US FDA, MHRA, and EU GMP standards, ensuring your systems, processes, and equipment are fully qualified and audit-ready.
Whether you’re commissioning a new system, expanding your facility, or maintaining ongoing compliance, we support every step of your validation lifecycle—from design qualification to requalification, process validation, and cleaning validation.
Thermal Validation
At VALQPRO LLP, we specialize in thermal validation to ensure the integrity and compliance of temperature-controlled equipment used in pharmaceutical, biotech, and healthcare industries. Our precise validation techniques help maintain regulatory compliance with standards such as US FDA, EU GMP, WHO, and ISO 17025.
HVAC Validation
At VALQPRO LLP, we specialize in clean room validation to ensure contamination control, environmental stability, and regulatory compliance in pharmaceutical, biotech, and healthcare industries. Our services help maintain adherence to ISO 14644, EU GMP, US FDA, and WHO guidelines for clean room environments.
Qualification
Our team of experienced validation professionals prepares and executes all critical qualification documents required during equipment and system lifecycle stages, including Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Requalification Services, Process Validation, Cleaning Validation