Worried about Sterility and Cross-Contamination? Ensure sterility with Alcami’s thorough Steam-in-Place Validation services and receive a detailed, expert-reviewed report after your system validation. Fast turnaround times keep your project on track. Trust Alcami for reliable and efficient Steam Quality Testing. Download the infographic to learn more > https://hubs.li/Q02L8dRK0 #Alcami #Sterilization #SteamQualityTesting #PharmaQuality #Validation #SQT #IQOQPQ
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Business Development Associate and Internal Sales Representative at Alcami Corporation
Concerned About Maintaining Sterility and Avoiding Cross-Contamination? Achieve assured sterility through Alcami's comprehensive Steam-in-Place Validation services, accompanied by an in-depth report reviewed by specialists post-validation. Quick processing times ensure your project remains on schedule. Depend on Alcami for dependable and effective Steam Quality Testing. Access the infographic for further details > https://gag.gl/gBPNme #Alcami #Sterilization #SteamQualityTesting #PharmaQuality #Validation #SQT #IQOQPQ
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Business Development Manager @ Alcami | Biotech Sales Professional | MS in Applied Life Sciences
Concerned about Maintaining Sterility and Avoiding Cross-Contamination? Achieve assured sterility through Alcami's comprehensive Steam-in-Place Validation offerings, complemented by an in-depth report reviewed by specialists post-validation. Quick processing times ensure your project remains on schedule. Depend on Alcami for dependable and effective Steam Quality Testing. Access the infographic for further information > https://gag.gl/gBPNme #Alcami #Sterilization #SteamQualityTesting #PharmaQuality #Validation #SQT #IQOQPQ
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Highly motivated PhD graduate with a deep passion for bioinformatics, virology, microbiology, immunology and the intricate dynamics of host-pathogen interactions
Highly recommend! Learned so much at this course!
!!! HURRY UP !!! There are still spots available for our last hPSC GMP Biomanufacturing Bootcamp of the year starting on December 11! 📢 Join us: https://lnkd.in/e_EMYFeR #biomanufacturing #celltherapy #advancedtherapies
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Another rewarding collaboration with my friend and fellow Stabilitarian, Kim HuynhBa. We discuss how the lifecycle concept discussed in ICH Q12 can be built into the stability program and support product and process changes from design through post-approval. For those interested, here is the link to the full article https://lnkd.in/eqQ5Akix
Managing Director; Adjunct Faculty; USP Council of Expert; AAPS Fellow; Editor-in-Chief of KENX Insight; GMP/QMS expert.
So excited to see in print a new publication that I have with Chris Latoz on Stability Lifecycle Management. #stability #lifecycle #ICHQ12 #pharmaceuticalindustry #FDA #NDA #ANDA Follow this link for the full paper. https://lnkd.in/eqQ5Akix
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Publisher / Sr. Business Development Manager , B2B Media Sales: Pharmaceutical Online , CellandGene- Life Science Connect Media
In Sterilize in Place (SIP) validation cycles, every detail is crucial. Every aspect, from the positioning to maintaining the integrity of biological indicators, must be precise; any deviation can result in erroneous outcomes and potential process risks. Numerous issues can be introduced by utilizing tape for positioning during SIP validation, ultimately undermining the process' validity. Continue reading to explore the top nine reasons why tape should not be relied upon during SIP validation cycles. #pharma #sterilization #validation Mesa Laboratories, Inc., Dan Johnson, Megan Wood, Crystal Sgrignoli Hostler
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👉Myth Of 3 Validation Batches? 👉Why we take 3 batches for Validation? 👉Any guidelines available for selection of Number of batches? 👉Why not less than 3 Batches? 👉Why not more than 3 Batches Read all these in following 👇👇👇👇👇👇👇👇👇👇👇👇👇👇👇 https://lnkd.in/d-BPeZF
Why Do We Use Three Batches For Validation?
pharmainform.com
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👉Myth Of 3 Validation Batches? 👉Why we take 3 batches for Validation? 👉Any guidelines available for selection of Number of batches? 👉Why not less than 3 Batches? 👉Why not more than 3 Batches Read all these in following 👇👇👇👇👇👇👇👇👇👇👇👇👇👇👇 https://lnkd.in/d-BPeZF
Why Do We Use Three Batches For Validation?
pharmainform.com
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👉Myth Of 3 Validation Batches? 👉Why we take 3 batches for Validation? 👉Any guidelines available for selection of Number of batches? 👉Why not less than 3 Batches? 👉Why not more than 3 Batches Read all these in following 👇👇👇👇👇👇👇👇👇👇👇👇👇👇👇 https://lnkd.in/d-BPeZF
Why Do We Use Three Batches For Validation?
pharmainform.com
-
👉Myth Of 3 Validation Batches? 👉Why we take 3 batches for Validation? 👉Any guidelines available for selection of Number of batches? 👉Why not less than 3 Batches? 👉Why not more than 3 Batches Read all these in following 👇👇👇👇👇👇👇👇👇👇👇👇👇👇👇 https://lnkd.in/d-BPeZF
Why Do We Use Three Batches For Validation?
pharmainform.com
