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How will green chemistry transform the future of pharma manufacturing

Express Pharma

A clear sign of this was provided by the citation for the 2005 Nobel Prize for Chemistry awarded to Chauvin, Grubbs, and Schrock, which commended their work as “a great step forward for green chemistry”. In recent years, pharma industry has been exploring the potential of green chemistry in drug manufacturing.

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An Annex 1 and Pharma 4.0 perspective on water quality

European Pharmaceutical Review

Her current research is focused on spectroscopy and mathematical modelling as process analytical technologies in pharmaceutical manufacturing. Inspection Technical Guide – Water for Pharmaceutical Use. Chemometrics and Intelligent Laboratory Systems , 2005, Årg. References. US Food and Drug Administration.

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IWD: Spotlight on women in life sciences

pharmaphorum

Darina Shopova (DS): My first job, in 2005, was as a structural CAD engineer in my home country of Bulgaria. DS: By constantly improving the design of our isolators, we are making pharmaceutical manufacturing more sustainable here at Envair Technology. What has your career path been? How did you get into life sciences?

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Ensuring Product Safety: U.S. FDA Guidance on Testing High-Risk Drug Components for Diethylene Glycol and Ethylene Glycol

Quality Matters

FDA guidance is an update to a guidance from 2005 and identifies not only DEG but also EG as potential contaminants in high-risk components including those listed in the title. Regulatory agencies in different countries can use the U.S.

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Corrective and Preventive Action (CAPA) Procedure for GMP

GMPSOP

ISO 9000:2005 Sec. You may have to qualify a new supplier, re-train the employees on operating procedures, re-validate the method to make it robust, or improve storage conditions, etc. Basically, you should take all sorts of preventive measures as directed by the outcomes of the investigation. What is corrective and preventive action?