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09 16 21 -- How To Find (and Manage) Biotech Consultants

09 16 21 -- How To Find (and Manage) Biotech Consultants
pharmaceuticalonline.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from pharmaceuticalonline.com Daily Mail and Mail on Sunday newspapers.

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08 19 21 -- Top Priorities And Challenges For New CDER Director Patrizia Cavazzoni, M D

08 19 21 -- Top Priorities And Challenges For New CDER Director Patrizia Cavazzoni, M D
pharmaceuticalonline.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from pharmaceuticalonline.com Daily Mail and Mail on Sunday newspapers.

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07 20 21 -- Qualification Considerations For A Factory-in-a-Box

07 20 21 -- Qualification Considerations For A Factory-in-a-Box
pharmaceuticalonline.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from pharmaceuticalonline.com Daily Mail and Mail on Sunday newspapers.

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06 17 21 -- From Pharma To Biopharma -- Education & Workforce Training Programs Converge To Meet Industry Needs

06 17 21 -- From Pharma To Biopharma -- Education & Workforce Training Programs Converge To Meet Industry Needs
pharmaceuticalonline.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from pharmaceuticalonline.com Daily Mail and Mail on Sunday newspapers.

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04 01 21 -- Auditing Electronic Batch Records For cGMP Status

04.01.21 Auditing Electronic Batch Records For cGMP Status Sponsor Pharmaceutical Online and Techceuticals, in collaboration with Federal Equipment Company, are excited to announce Virtual Pharma Expo: Oral Solid Dose Manufacturing. Don’t miss this FREE LIVE event on May 5th & 6th featuring 15-minute presentations with leading OSD packaging and process equipment manufacturers. Register Now. Featured Editorial By Tim Sandle, Ph.D., Bio Products Laboratory Ltd. This article presents some advice for auditing electronic batch records to assess their cGMP status. This is useful in the qualification stage and essential once the electronic record system is in operation. Industry Insights Article

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