Releasing Services

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Supporting Services

Our team of Qualified Persons (QPs) brings extensive experience and expertise in pharmaceutical regulations and market release processes.

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.

Releasing services include

Our Qualified Persons perform thorough reviews and assessments of manufacturing records, analytical data, and quality documentation to certify the release of pharmaceutical batches for distribution and sale.

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 QPs verify the quality, safety, and efficacy of pharmaceutical products, providing assurance to regulatory authorities, healthcare professionals, and patients.

Do you have any questions? 

Reach out to our team today for personalized assistance.

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