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12 14 21 -- How To Enable Your Quality Risk Management Lifecycle

12/14/21 Pharmaceutical Online Newsletter

Jakob bondeTristan wilkinsPaola lazzeriAnna campanellaGiulia artalliEli lillyAllison alixWebinar catalentVan daelenLee allenJacqueline hargisLloyd magerFrank panofenMegan masonAndrea engelSharon nowak

EU GMP Annex 1 Non-Viable Environmental And Process Monitoring Insights And Updates

The 2020 release of the EU GMP Annex 1 draft includes a new chapter on viable and non-viable environmental and process monitoring. This paper covers.

Anna campanellaPaola lazzeriGiulia artalliFrank panofenDaniele pandolfiMaurizio della pietra

Classification Qualification And Monitoring According To EU GMP Annex 1 Rev 12

Classification Qualification And Monitoring According To EU GMP Annex 1 Rev 12
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.

Life sciences divisionMaurizio della pietraProduct line managerLife sciences

09 24 21 -- 5 Misconceptions About Data Integrity In Pharma

09 24 21 -- 5 Misconceptions About Data Integrity In Pharma
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.

Maysam sodagariPaola lazzeriAnna campanellaOliver staufferGiulia artalliSpencer bolteHemi sagiFrank panofenMatt smithAndy gollYves massicotteJustin kadisAndreas meudtJohn erdnerSharon nowakDaniele pandolfi

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

Comunidad autonoma de catalunaPaul magretaMajaz hussainBrian stephensMukta acharyaJessica settimiQuadro comilCase study seeq corporationCase study flow sciences incEquipment companyArticle promega corporationApplication note silverson machines incSamira shoreThermo fisherJohn barleyGrifols recombinant protein

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