ISO 13485:2016
This course gives a detailed introduction to the standard and gives the partici- pants a solid knowledge of the standard content and how they should
Pharma 4ever er specialiseret i konsulentarbejde for medicinal-, biotek- og medicinsk udstyrsvirksomhed
Pharma4ever is your daily engineering or QA partner in the pharmaceutical and medical device industry.
We see it as our mission to provide key resources for your project.
Pharma4ever has more than 477 years of experience in the pharmaceutical field in Denmark across more than 25 profiles spanning over Process Engineering, Finished Product Engineering and Device areas.
This base of experience, as well as our network of external partners, enables us to deliver the profiles you are looking for.
Let us talk about the possibilities for filling your needs for your project.
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This course gives a detailed introduction to the standard and gives the partici- pants a solid knowledge of the standard content and how they should
This course goes through the different development phases and the different key documents for each development phase; from Design Planning to Design Transfer.
Are you ready to become part of our team of highly skilled specialists? And do you want to make your automation knowledge count as you
Would you like to make your expert process knowledge count as you make a difference for our clients within the pharmaceutical industry? Are you fed
Are you well versed in the art of cleaning and sterilization for equipment and processes? And would you like to put that knowledge to good
This course is focusing on European approval process and the content of the Medical Device Regulation (MDR), but is also introducing the FDA approval process.
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