IT Quality, Validation, and Compliance Consultant

Pharma IT Careers IT Quality, Validation, and Compliance Consultant January 18, 2023 Location: Denmark Application deadline: ASAP Pharma IT Careers IT Quality, Validation, and Compliance Consultant January 18, 2023 Location: Denmark ← Back to careers Share on email Share on linkedin Share on twitter Share on skype Share on facebook Are you a detail-oriented, quality-conscious …

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Serialization in Brazil – this time it is for real.

With legislation dating back to January 2009, requirements for serialization and reporting in Brazil has been underway for a long time now. Those of us having worked with serialization for a while, may remember working feverishly in second half of 2015 to comply with an almost impossibly complex set of requirements. The goal at the …

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EU MDR postponed until 26 May 2021. Relax, plenty of time?

The full implementation of the EU MDR (Medical Device Regulation) was recently postponed until 26-May 2021 and for any Medical Device company that wants to sell their products in the European Marketplace, they have to be compliant with MDR. So, now you have plenty of time to get fully compliant with MDR? Not really, I’m …

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Handling sensitive patient data in the US – Guide to HIPAA Compliance

In the following post Pharma IT will describe the content of the HIPAA legislation and give some points to what is important in respect to implementation of HIPAA compliance. Should you need assistance to establish HIPAA compliance in your organisation, please contact us HIPAA – the Health Insurance Portability and Accountability Act sets the standard …

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