In November 2017, the European Commission published a set of new guidelines on Good Manufacturing Practices (GMP) specific to advanced therapy medicinal products (ATMPs). 

Below, seQure Life Sciences created a summary about the new New Guidelines on Good Manufacturing pratices for advanced therapies:

Good Manufacturing Practices

To download our infographic, click here.

Who is seQure Life Sciences
seQure is a niche services provider operating in the Life Sciences sector. seQure provides expert pharmacovigilance, quality management and assurance, regulatory and computer system validation solutions to drug and device companies to help them meet regulatory requirements. seQure services are provided as consultancy, as projects or in a functional service provision model. The company strives to meet specific needs of clients in the following sectors: pharmaceutical, biotechnology, medical device, academic institutions and associations as well as CROs (Contract Research Organizations) and Service Providers.

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