19: The important role of AI in TMF oversight
PharmaLex Talks24 Touko 2023

19: The important role of AI in TMF oversight

Artificial intelligence is playing an increasingly important role in document management in the life sciences industry and in particular in improving management and oversight of the Trial Master File (TMF). The podcast explores why and how AI is a gamechanger for the TMF and what it means for pharmaceutical companies now and in the future.

Bio:
Jim Horstmann is Product Manager of Clinical Products at Phlexglobal where he draws on his extensive experience in document management solutions that comply with health authority regulations while also being easy to use and interoperable with other systems. For the past 11 years, Jim has focused primarily on electronic Trial Master File solutions. He is passionate about optimizing business processes by leveraging technology to help make organizations more efficient and productive.
For more information about how AI is used PhlexTMF, please visit https://www.phlexglobal.com/

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Jaksot(37)

29: Exploring the interactions between validation and technology transfer

29: Exploring the interactions between validation and technology transfer

Synopsis: In this podcast, Gerardo Gomez talks about the interactions between validation and technology transfer, considering the views and expectations of the regulators. As Gerardo explains, technol...

24 Tammi 202413min

28: Early access programs: What they are and how to plan for them

28: Early access programs: What they are and how to plan for them

Synopsis: Early access programs are designed to allow patients suffering from a life-threatening unmet medical need or disease to be given promising treatments that have not yet received marketing app...

5 Joulu 202315min

27: Assessing gaps and achieving compliance with Annex 1

27: Assessing gaps and achieving compliance with Annex 1

Bio Patrick Nieuwenhuizen Quality professional with a Microbiology & Sterile Manufacturing background with over 25 years’ experience in the Pharmaceutical Industry. Worked for several global Pharmace...

28 Marras 202315min

26: Navigating the Process of Technology Transfer

26: Navigating the Process of Technology Transfer

Synopsis: Technology transfer involves two main types: scale-up and transfer to a different site. Scale-up technology transfer involves moving a technology or process from a laboratory or pilot-scale ...

14 Marras 202318min

25: Scaling Patient Safety through Innovation

25: Scaling Patient Safety through Innovation

Bio: Michael Braun-Boghos Michael has been working in medicinal product safety for the last three decades. He spent 13 years at the European PV headquarters of Fujisawa, which later became Astellas, ...

25 Syys 202316min

24: Why Early Phase Modeling is Key to Reimbursement and Patient Access

24: Why Early Phase Modeling is Key to Reimbursement and Patient Access

Market access can be a big hurdle for companies to overcome and might require a different approach to the process of gathering evidence to support reimbursement discussions. Early phase modeling can h...

12 Syys 202311min

23: The Unique and Complex World of Combination Products

23: The Unique and Complex World of Combination Products

Combination products offer unique advantages in terms of delivering improved therapeutic outcomes or enhanced patient convenience. Typically, combination products are understood to be a drug-device or...

31 Elo 202310min

22: Avoiding Pitfalls with your Product Development Strategy

22: Avoiding Pitfalls with your Product Development Strategy

Companies often fall into common traps in early-stage product development. These range from interactions with the regulators to their ability to manufacture their product. Forward planning is crucial,...

2 Elo 202312min

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