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Session by Dr Ranjit Barshikar, CEO-QbD International; United Nations Adviser - Geneva
⏲ 11 min 53 sec ✓ 16-Dec-2021
Patti Cochrane (Trillium Health Centre) - QBD Interview (April 17, 2008)
⏲ 19 min 37 sec ✓ 17-Aug-2010
Pfizer, Inc.'s Approach to Quality By Design in Clinical Trials
⏲ 1 min 69 sec ✓ 30-Jan-2013
Opening presentation QbD framework.mp4
⏲ 36 min 69 sec ✓ 19-Apr-2022
Advancing Gene Therapy - A Quality by Design Approach
⏲ 7 min 58 sec ✓ 04-Dec-2021
QBD DRILL TAPE 2020: FTG'S
⏲ 42 sec ✓ 03-Jul-2020
QbD-Expert™ Software : Live Video Promo �️
⏲ 2 min 77 sec ✓ 08-Feb-2018
Raphael Liogier Chaire J. Leclercq UCL 4 5 : Analyse critique des trois thèmes propres à la technoscience déreconstructive
⏲ 93 min 30 sec ✓ 18-Mar-2016
Patient Advocates in Improving the Quality of Clinical Trials by Carol Matyka
⏲ 80 sec ✓ 30-Jan-2013
QBD_Sync
⏲ 1 min 97 sec ✓ 03-Feb-2023
MEGGLE: Co-processed Excipients
⏲ 55 sec ✓ 13-Oct-2020
Panel: Looking Forward - Where are Biopharmaceutical Manufacturers Going, and How Should We Get There?
⏲ 22 min 19 sec ✓ 15-Dec-2016
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_session-by-dr-ranjit-barshikar-ceo-qbd-international-united-nations-adviser-geneva.webp "In this video:nSession: Dr Ranjit Barshikar, CEO-QbD International; United Nations Adviser - GenevanTopic: Automation and AI for Formulations Development")
_patti-cochrane-trillium-health-centre-qbd-interview-april-17-2008.webp "Patti Cochrane (Trillium Health Centre) - QBD Interview (April 17, 2008) from qbd")
_pfizer-inc-39s-approach-to-quality-by-design-in-clinical-trials.webp "This video pertains to CTTI's QbD & QRM Project: http://www.ctti-clinicaltrials.org/what-we-do/investigational-plan/qbd-qrmnn*The views and opinions expressed in this video are those of the speaker and do not necessarily reflect the official policy or position of CTTI.")
_opening-presentation-qbd-framework-mp4.webp "Opening presentation QbD framework.mp4 from qbd")
_advancing-gene-therapy-a-quality-by-design-approach.webp "Do you already have a sound Chemistry, Manufacturing and Controls (CMC) strategy to guide your gene therapy development process? nIn this episode Peiqing Zhang speaks about some of the recent regulatory setbacks for gene therapy programs. He notes that one of the main reasons is gaps in the CMC section of the regulatory submission and that interpretation and implementation of guidelines released for gene therapy seem to be unclear to the industry. nnPall recently published a Quality by Design")
_qbd-drill-tape-2020-ftg39s.webp "QBD DRILL TAPE 2020")
_qbd-expert-software-live-video-promo.webp "� � Presenting Live Promo of nQbD-Expert (Quality by Design) Software nnQbD-Expert™, is a World’s First USFDA 21CFR11 Compliant Software Application for Pharma “Quality by Design (QbD)” for designing & development of pharmaceutical dosage forms, offers in built Readymade Modules with Customizable Templates for 150 different pharma formulations comprising of: (A) Solid Orals (Tablets IR / MR, MUPS, Hard Gelatin & SoftGel Capsules), (B) Liquid Orals (Solution, Suspension, Emuls")
_raphael-liogier-chaire-j-leclercq-ucl-4-5-analyse-critique-des-trois-thmes-propres-la-technoscience-dreconstructive.webp "La technoscience du XXIème siècle bouleverse-t-elle la structure de la narration humaine ?nLe corps :n- Corps, chair, morphologie, forme et transformationn- L’homme physiquement augmentén- Physiologie et physionomie (qu’est-ce qu’un corps ? La question du périmètre nerveux) - Le rapport à l’espacen- Le corps signe d’autre que lui-mêmen- Performance et esthétique corporellesnLa conscience :n- L’intelligence augmentée : définitions et paradoxesn- L’intelligence artifici")
_patient-advocates-in-improving-the-quality-of-clinical-trials-by-carol-matyka.webp "National Breast Cancer Coalition Advocate Carol Matyka discusses the importance of having patients involved in improving the quality of the clinical trials process. nnThis video pertains to CTTI's QbD & QRM Project: http://www.ctti-clinicaltrials.org/what-we-do/investigational-plan/qbd-qrmnn*The views and opinions expressed in this video are those of the speaker and do not necessarily reflect the official policy or position of CTTI.")
_qbd-sync.webp "QBD_Sync from qbd")
_meggle-co-processed-excipients.webp "MEGGLE has it. The right co-processed excipients for direct compressionnnThe use of co-processed excipients (CPE) are by far the easiest and fasted way to develop solid oral dosage forms.nnThe solution: Co-processed excipientsnnTraditional excipients struggle to cope with current challenges in drug development such as high speed tableting, developing direct compression formulation, low dose related content uniformity issues and insufficient tablet hardness due to high dose loading. Co-processed")
_panel-looking-forward-where-are-biopharmaceutical-manufacturers-going-and-how-should-we-get-there.webp "• Talking about the state of the biotech industry today: Which emerging trend will see the most growth?n• People and technology: How are these forces working together to grow and mature our industry?n• Discussing challenges in capacity planning, make-buy decisions, and supply chain managementn• What is the next big challenge and the next big opportunity facing our community? Are we ready for it?nn--nnModerator: nnPatrick Yang, Former EVP, Technical Operations, GenentechnnDr. Patrick Y. Y")
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