Comprehensive IQ/OQ/PQ validation services ensuring your pharmaceutical equipment meets FDA, EMA, and global regulatory requirements. Complete documentation packages and expert validation support.
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FDA-compliant validation protocols ensuring regulatory compliance and operational excellence.
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Our validation services ensure compliance with pharmaceutical regulations worldwide, including FDA (USA), EMA (Europe), Health Canada, TGA (Australia), and other international standards.
Electronic records and signatures validation for US market requirements.
European Medicines Agency qualification and validation guidelines.
Good automated manufacturing practice for computerized systems.
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Contact our validation specialists to discuss your equipment qualification requirements and ensure regulatory compliance for your pharmaceutical operations.
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