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12 23 21 -- Tips For Risk Facilitators Conducting Remote Sessions

12/23/21 Pharmaceutical Online Newsletter

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Key Equipment Sourcing Strategies For Contract Manufacturing Organizations (CMO s)

Key Equipment Sourcing Strategies For Contract Manufacturing Organizations (CMO s)
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David winger

07 30 21 -- 8-Step Checklist To Write Effective Investigation Reports

07 30 21 -- 8-Step Checklist To Write Effective Investigation Reports
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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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