Articles Tagged: Pharmaceutical Manufacturing

How Digital Batch Management Improves Efficiency and Consistency

I’ve discussed some of the new regulations facing the pharmaceutical industry in past posts. Some of these regulations, like data integrity, are relatively consistent across the globe while others, like… Read more »

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Three Ways to Improve Regulatory Compliance in Pharmaceutical Manufacturing

Pharmaceutical companies in the market today need to comply with a huge array of regulations –in most regions, manufacturers must follow Good Manufacturing Practice (GMP), as well as Good Documentation… Read more »

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5 Questions to Ask in a Serialization Journey

In a prior blog post I discussed how serialization in the world of prescription drugs provides end-to-end product integrity as it tracks and authenticates each change of ownership of the product… Read more »

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Serialization Plays a Key Role in Track and Trace

With the pharmaceutical supply chain becoming longer and more complex than ever, opportunities for counterfeiting, gray marketing or product mix-ups of prescription drugs is at an all-time high. With a… Read more »

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Looking Ahead: Best Practices #7 and #8 for Retrofitting Your Pharmaceutical Manufacturing Facility

Written by Guest Blogger, Richard Parapar Throughout this series, we’ve covered six of the eight best practices for retrofitting an automated pharmaceutical manufacturing facility. In this installment, we’ll cover the… Read more »

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Getting Educated, Getting Involved: Best Practices #5 and #6 for Retrofitting Your Pharmaceutical Manufacturing Facility

Written by Guest Blogger, Richard Parapar In our last installment, we covered the third and fourth best practices adopted by Genentech and proven to be effective in retrofitting pharmaceutical manufacturing… Read more »

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Data, Development, and Documentation: Best Practices #3 and #4 for Pharmaceutical Manufacturing Retrofit

Written by Guest Blogger, Richard Parapar In our last blog, we provided an introduction to the first two of eight best practices for effectively retrofitting manufacturing systems in a pharmaceutical… Read more »

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Getting Started: Best Practices #1 and #2 for a Pharmaceutical Manufacturing Upgrade Project

Written by Guest Blogger, Richard Parapar It’s hard to address flaws in an existing system if you don’t know what they are. And the more information that a facility has… Read more »

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Genentech: How One Company Made Retrofitting Work

Written by Guest Blogger, Richard Parapar Genentech is a pharmaceutical company best known for their groundbreaking cancer treatments. Their CCP1 facility— that is, their first large-scale cell culture production facility—… Read more »

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Genentech: How One Company Made Retrofitting Work

Written by Guest Blogger, Richard Parapar Genentech is a pharmaceutical company best known for their groundbreaking cancer treatments. Their CCP1 facility— that is, their first large-scale cell culture production facility—… Read more »

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Getting Started: Best Practices #1 and #2 for a Pharmaceutical Manufacturing Upgrade Project

Written by Guest Blogger, Richard Parapar It’s hard to address flaws in an existing system if you don’t know what they are. And the more information that a facility has… Read more »

Leave a comment

Data, Development, and Documentation: Best Practices #3 and #4 for Pharmaceutical Manufacturing Retrofit

Written by Guest Blogger, Richard Parapar In our last blog, we provided an introduction to the first two of eight best practices for effectively retrofitting manufacturing systems in a pharmaceutical… Read more »

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Looking Ahead: Best Practices #7 and #8 for Retrofitting Your Pharmaceutical Manufacturing Facility

Written by Guest Blogger, Richard Parapar Throughout this series, we’ve covered six of the eight best practices for retrofitting an automated pharmaceutical manufacturing facility. In this installment, we’ll cover the… Read more »

2 Comments

Getting Educated, Getting Involved: Best Practices #5 and #6 for Retrofitting Your Pharmaceutical Manufacturing Facility

Written by Guest Blogger, Richard Parapar In our last installment, we covered the third and fourth best practices adopted by Genentech and proven to be effective in retrofitting pharmaceutical manufacturing… Read more »

Leave a comment

5 Questions to Ask in a Serialization Journey

In a prior blog post I discussed how serialization in the world of prescription drugs provides end-to-end product integrity as it tracks and authenticates each change of ownership of the product… Read more »

Leave a comment

Serialization Plays a Key Role in Track and Trace

With the pharmaceutical supply chain becoming longer and more complex than ever, opportunities for counterfeiting, gray marketing or product mix-ups of prescription drugs is at an all-time high. With a… Read more »

Leave a comment

Three Ways to Improve Regulatory Compliance in Pharmaceutical Manufacturing

Pharmaceutical companies in the market today need to comply with a huge array of regulations –in most regions, manufacturers must follow Good Manufacturing Practice (GMP), as well as Good Documentation… Read more »

Leave a comment

How Digital Batch Management Improves Efficiency and Consistency

I’ve discussed some of the new regulations facing the pharmaceutical industry in past posts. Some of these regulations, like data integrity, are relatively consistent across the globe while others, like… Read more »

Leave a comment

Looking Ahead: Best Practices #7 and #8 for Retrofitting Your Pharmaceutical Manufacturing Facility

Written by Guest Blogger, Richard Parapar Throughout this series, we’ve covered six of the eight best practices for retrofitting an automated pharmaceutical manufacturing facility. In this installment, we’ll cover the… Read more »

2 Comments

Data, Development, and Documentation: Best Practices #3 and #4 for Pharmaceutical Manufacturing Retrofit

Written by Guest Blogger, Richard Parapar In our last blog, we provided an introduction to the first two of eight best practices for effectively retrofitting manufacturing systems in a pharmaceutical… Read more »

Leave a comment

Getting Educated, Getting Involved: Best Practices #5 and #6 for Retrofitting Your Pharmaceutical Manufacturing Facility

Written by Guest Blogger, Richard Parapar In our last installment, we covered the third and fourth best practices adopted by Genentech and proven to be effective in retrofitting pharmaceutical manufacturing… Read more »

Leave a comment

Serialization Plays a Key Role in Track and Trace

With the pharmaceutical supply chain becoming longer and more complex than ever, opportunities for counterfeiting, gray marketing or product mix-ups of prescription drugs is at an all-time high. With a… Read more »

Leave a comment

5 Questions to Ask in a Serialization Journey

In a prior blog post I discussed how serialization in the world of prescription drugs provides end-to-end product integrity as it tracks and authenticates each change of ownership of the product… Read more »

Leave a comment

Three Ways to Improve Regulatory Compliance in Pharmaceutical Manufacturing

Pharmaceutical companies in the market today need to comply with a huge array of regulations –in most regions, manufacturers must follow Good Manufacturing Practice (GMP), as well as Good Documentation… Read more »

Leave a comment

How Digital Batch Management Improves Efficiency and Consistency

I’ve discussed some of the new regulations facing the pharmaceutical industry in past posts. Some of these regulations, like data integrity, are relatively consistent across the globe while others, like… Read more »

Leave a comment

Genentech: How One Company Made Retrofitting Work

Written by Guest Blogger, Richard Parapar Genentech is a pharmaceutical company best known for their groundbreaking cancer treatments. Their CCP1 facility— that is, their first large-scale cell culture production facility—… Read more »

Leave a comment

Getting Started: Best Practices #1 and #2 for a Pharmaceutical Manufacturing Upgrade Project

Written by Guest Blogger, Richard Parapar It’s hard to address flaws in an existing system if you don’t know what they are. And the more information that a facility has… Read more »

Leave a comment