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Gert Moelgaard is vice president for strategic development in NNE Pharmaplan.
He has worked in the pharmaceutical industry for more than 25 years and has
experience from a number of major engineering, automation and validation projects within pharmaceutical manufacturing as well as senior management positions.
Gert has made contributions at international conferences on automation,
GAMP (Good Automated Manufacturing Practice), process validation, PAT (process analytical tool), manufacturing excellence and Quality by Design and a wealth of other topics.
He has also contributed to several books and technical guidelines.
Gert is a past chairman of ISPE (International Society of Pharmaceutical Engineering) and has been very closely involved in ISPE's cooperation with industry and regulators, especially on the science and risk based approach and the Quality by Design (QbD) paradigm of pharmaceutical R&D and manufacturing. He is on the steering committee of ISPE's Community of Practice for Commissioning and Qualification and is currently involved in the training of FDA's field investigators on the new FDA process validation guidance.
You can contact Gert on: +45 3079 2775
Visit Gert's profile on LinkedIn
Gert's upcoming events
The list below shows upcoming events at which Gert is speaking or engaged in otherwise.
| Event: |
The pharmaceutical industry at a crossroad |
| |
Gert will give a presentation adressing the main challenges for companies in today's pharmaceutical markets |
| When: |
7 June 2012 |
| Where: |
Lund, Sweden |
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| Event: |
The pharmaceutical industry at a crossroad |
| Description: |
Gert will give a presentation adressing the main challenges for companies in today's pharmaceutical markets |
| When: |
8 June 2012 |
| Where: |
Uppsala (morning) and Stockholm (afternoon), Sweden |
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| Event: |
ACHEMA 2012 |
| Description: |
Gert will give a presentation titled "Trends in the pharmaceutical industry" |
| When: |
19 and 20 June 2012 |
| Where: |
Frankfurt, Germany |
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