Moelgaard Consulting is specialised within consulting services within pharmaceutical manufacturing, technology and GMP compliance. The services are based on more than 30 years experience in the pharmaceutical industry, mainly from Novo Nordisk, NNE Pharmaplan and Vetter Pharma Fertigung.
The services are related to the practical application of modern process validation, pharmaceutical manufacturing technology and automation as well as training and workshops on implementation.
Active engagement in the advances of the pharmaceutical industry within technology, manufacturing and compliance internationally with regulators and professional organisations. Through engagements in workshops, courses and conferences and the development and implementation of new guidelines within pharmaceutical manufacturing and compliance in ISPE, PDA and ECA (European Compliance Academy).
“The life science industry is undergoing some very big changes that hold a lot of business opportunities if handled right. However, there are some significant challenges for pharmaceutical companies in becoming global, staying in compliance and achieving operating efficiency. There is a lot of work to be done”
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