CPhI Pharma Evolution Guest Post-Electronic Batch Records: Are Your Systems...
I wanted to share my guest post published at the CPhI Pharma Evolution website. There are some great comments, so join in if the post sparks some ideas. Stringent inspection-readiness policies are...
View ArticleGood Manufacturing Practice Background and Overview
Highly regulated industries, such as pharmaceutical and biotech manufacturing, face a myriad of compliance issues, which vary by region of the world and continuously involve. Emerson’s Heather Schwalje...
View ArticleManaging Asset Performance and Collaborating in the Life Science Industry
In two very different industries, I have some updates to share from Emerson consultants. On the reliability front, when we last checked in with Emerson’s Richard Barnes, a Senior Asset Optimization...
View ArticleElectronic Batch Record Design Considerations
Last week, the 2nd International Summit on GMP, GCP & Quality Control was held in Chicago, Illinois USA. Emerson’s Heather Schwalje, a senior Life Sciences consultant, presented Moving beyond part...
View ArticleCPhI Pharma Evolution Guest Post-Electronic Batch Records: Are Your Systems...
I wanted to share my guest post published at the CPhI Pharma Evolution website. There are some great comments, so join in if the post sparks some ideas. Stringent inspection-readiness policies are...
View ArticleGood Manufacturing Practice Background and Overview
Highly regulated industries, such as pharmaceutical and biotech manufacturing, face a myriad of compliance issues, which vary by region of the world and continuously involve. Emerson’s Heather Schwalje...
View ArticleManaging Asset Performance and Collaborating in the Life Science Industry
In two very different industries, I have some updates to share from Emerson consultants. On the reliability front, when we last checked in with Emerson’s Richard Barnes, a Senior Asset Optimization...
View ArticleElectronic Batch Record Design Considerations
Last week, the 2nd International Summit on GMP, GCP & Quality Control was held in Chicago, Illinois USA. Emerson’s Heather Schwalje, a senior Life Sciences consultant, presented Moving beyond part...
View ArticleCPhI Pharma Evolution Guest Post-Electronic Batch Records: Are Your Systems...
I wanted to share my guest post published at the CPhI Pharma Evolution website. There are some great comments, so join in if the post sparks some ideas. Stringent inspection-readiness policies are...
View ArticleGood Manufacturing Practice Background and Overview
Highly regulated industries, such as pharmaceutical and biotech manufacturing, face a myriad of compliance issues, which vary by region of the world and continuously involve. Emerson’s Heather Schwalje...
View ArticleManaging Asset Performance and Collaborating in the Life Science Industry
In two very different industries, I have some updates to share from Emerson consultants. On the reliability front, when we last checked in with Emerson’s Richard Barnes, a Senior Asset Optimization...
View ArticleElectronic Batch Record Design Considerations
Last week, the 2nd International Summit on GMP, GCP & Quality Control was held in Chicago, Illinois USA. Emerson’s Heather Schwalje, a senior Life Sciences consultant, presented Moving beyond part...
View Article
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