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Corona Vaccine Production

GMP compliance

Genre: mRNA vaccine
Published: 2021
Length: 1h 11min
Keywords: GCP, GMP, GDP, Qualification/Validation, QC, mRNA vaccine

BioNTech has acquired Novartis plant in Marburg for large scale manufacturing of Corona vaccines [1]. This current approach represents innovative but also risky procedure since vaccine candidate must be approved and production line must be inspected by authority.

In order to receive authorial permission to produce this vaccine, several things must be performed to establish GMP compliance. These aspects are then subject of authorial inspection representing prerequisite for receiving manufacturing license in Germany.

In this seminar you will learn all relevant issues to qualify a production plant for pharmaceuticals based on this prominent case study for large scale mRNA vaccine manufacturing. This theoretical approach will illustrate authorial requirements for pharma production and general drug approval.

Teaching goals [printed on certificate]:

-approval of pharmaceuticals (vaccines) in Germany and EU

-clinical trials and GCP compliance

-from pilot scale to large scale

-qualification of large scale production to GMP compliance (vaccines)

 

Participation in this seminar includes success control and receive of certificate of completion including all relevant keywords for your records.

[1]
https://www.fiercepharma.com/manufacturing/biontech-buys-novartis-plant-for-covid-19-vaccine-eyes-capacity-up-to-750m-doses

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