Contract development & Manufacturing Services
Releasing Services
Our team of Qualified Persons (QPs) brings extensive experience and expertise in pharmaceutical regulations and market release processes.
Ensuring the safe and compliant release of every pharmaceutical product
At Tiofarma, we conduct comprehensive reviews and evaluations of manufacturing records, analytical data, and quality documentation to certify the release of pharmaceutical batches for distribution and sale. We verify the quality, safety, and efficacy of pharmaceutical products, providing assurance to regulatory authorities, healthcare professionals, and patients. We ensure that all market release activities comply with relevant regulatory requirements, including Good Manufacturing Practice (GMP) guidelines, EU regulations, and other applicable standards.
Our releasing services cover the full scope of batch certification, regulatory compliance, and product quality assurance. Our Qualified Persons conduct detailed reviews of manufacturing records, analytical data, and quality documentation to certify each batch for distribution. They ensure that all release activities meet GMP, EU, and other regulatory standards, while verifying the quality, safety, and efficacy of every product to provide confidence to regulators, healthcare professionals, and patients.
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