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PODCAST

From Concept to Medicine - A Comprehensive Drug Development Journey

Welcome to a Complete Drug Development Journey!Have you ever wondered how groundbreaking medicines go from a scientist’s vision to life-saving treatments in hospitals and pharmacies worldwide? The journey of drug development is an intricate, high-stakes adventure—filled with scientific breakthroughs, regulatory twists, and the relentless pursuit of innovation.In this podcast, we take you behind the scenes of pharmaceutical research and development, unraveling the complex and fascinating process that

science chemistry

All Episodes

14:02

150 – Season 10 Recap & Vision Forward (S10E15)

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

Recap key digital innovations discussed and outline how technology will continue to shape pharma. Summary dialogue linking current trends to future developments. Pull real world literature examples from your OPR&D sources where appropriate.The listeners are more and more able to see the future of what will be. The big thanks to everyone who helped get this to where it needed to get to.

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9:31

149 – Future Trends in Digital Pharma (S10E14)

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

Highlight emerging digital trends set to further transform drug development over the next decade. Conversation on innovations and long-term impacts supported by case studies. Pull real world literature examples from your OPR&D sources where appropriate.The ultimate goal is to figure it all out and see if we can all be as successful as possible. This episode will give you something special that you can find in a lot of organic chemistry.

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11:19

148 – Regulatory Considerations for Digital Health...

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

Review how regulators address digital health tools and data in the context of drug development. Dialogue on evolving guidelines and compliance challenges with real-world cases. Pull real world literature examples from your OPR&D sources where appropriate.The goal of the talk is to try and stay up to date on what has been going on and what is the most relevant. You will know more now. This has been a short dive and all people on board were ready to dive!

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14:36

147 – Telemedicine & Decentralized Trials (S10E12)

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

Explore the shift toward telemedicine and decentralized clinical trials that broaden patient participation. Dialogue on logistics, technology, and regulatory considerations with practical examples. Pull real world literature examples from your OPR&D sources where appropriate.You are able to see how you are helping more people. Now is the time to lean on the process, but you do not always have. The good news is that you can and should be helping more people.

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12:03

146 – Wearable Technology & Patient Monitoring (S10E11)

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

Discuss how wearable devices capture real-time patient data to monitor treatment responses during trials. Conversation on device integration, data use, and improved patient outcomes. Pull real world literature examples from your OPR&D sources where appropriate.It allows you to show a Doctor, or even a patient the way it would help, and it will be great in understanding why people need the medicine. What’s good about the VR is that we can get people to have a huge reaction in a short amount of

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21:33

145 – Case Study: Digital Innovation Accelerating R&D...

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

Present a case study illustrating how digital tools accelerated R&D, from discovery to process optimization. Narrative highlighting benefits and challenges drawn from actual projects. Pull real world literature examples from your OPR&D sources where appropriate.This episode can be used for what’s been already in AR & VR in Pharma! We want to pull out all the key stuff, using examples where we can maybe even linking back to things like OPRD literature if it fits, right. Connect the dots a

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11:59

144 – Big Data & Real-World Evidence (S10E9)

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

Explore how big data analytics is transforming the use of real-world evidence in decision-making and drug development. Dialogue on data sources, analytic platforms, and outcome examples. Pull real world literature examples from your OPR&DThis discussion goes into detail about drug development, manufacturing processes, and why you would use blockchain for it! This helps ground all that you would be doing.

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13:27

143 – Cloud Computing & Data Security (S10E8)

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

Explain how cloud computing supports data storage and analysis in pharma while emphasizing cybersecurity. The discussion on data management practices and regulatory considerations. Pull real world literature examples from your OPR&D sources where appropriate.This episode will give an opportunity to see what’s been working already in other sectors and what can be integrated into the Pharma field to take things to the next level. This opportunity is one in which the listeners can learn about where

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13:23

142 – IoT & Smart Manufacturing (S10E7)

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

Discuss the integration of IoT devices in manufacturing to monitor equipment performance and process consistency. This will have conversation on sensor technology and data integration with documented examples. You can pull real world literature examples from your OPR&D sources where appropriate.This topic will make you thankful for things to be more accurate and will be in touch with the spirit of R&D. The listener has the opportunity to dive into a way to learn more which might impact the

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17:44

141 - Real-Time Data Analytics in Clinical Trials...

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

Explore how real-time analytics improve trial monitoring, patient recruitment, and adaptive decision-making. This discussion looks at digital tools and their impact on trial efficiency with case studies. Real world literature examples pull from your OPR&D sources where appropriate.This episode takes a look at how real-time analytics can help spot subtle things a regular human may not. This would be great for patient safety, if there were a way to determine that and could help speed up the

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11:25

140 – Digital Twins in Process Development (S10E5)

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

Introduce digital twins as virtual replicas of manufacturing processes that aid in optimization and troubleshooting. This dialogue contains on simulation benefits and predictive maintenance with illustrative examples. Real world literature examples are then pulled from your OPR&D sources where appropriate.This episode takes a look into this area more specifically, digital twins are not just Sci-fi! They actually have 2 main jobs. One being more proactive troubleshooting.

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13:28

139 - Blockchain for Supply Chain Transparency (S10E4)

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

Explain how blockchain enhances supply chain security and traceability in drug manufacturing. This discussion on implementation challenges and benefits for compliance with real-world cases. Real world literature examples pulls from your OPR&D sources where appropriate.In this podcast the listener learns that the implementation for a big change is not a simple one to take on. They also learn that it all has benefits. The listener is sure to remember that blockchain could provide all that hard

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11:56

138 - Virtual & Augmented Reality in Pharma (S10E3)

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

This episode delves into the transformative applications of Virtual Reality (VR) and Augmented Reality (AR) tools within the pharmaceutical industry. The discussion includes their use in training, design simulations, and visualizing intricate molecular interactions. Explored are VR for designing drug delivery devices and also augmented reality in existing placesThe analysis includes the exploration of practical applications and future potential, supported by concrete examples. It aims to provide

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13:04

137 – AI & Machine Learning in Drug Discovery (S10E2)

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

Explore the transformative role of AI and machine learning in predicting drug-target interactions and optimizing candidate selection, revolutionizing traditional methods. Dialogue on algorithm development, data mining, and detailed case examples, offering practical insights into the application of these technologies in the pharmaceutical industry. Real world literature examples pulled from OPR&D sources where appropriate, grounding the discussion in tangible results and current industry

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11:05

136 - Digital Transformation in Pharma (S10E1)

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/17

This episode introduces how digital technologies are revolutionizing the pharmaceutical industry, from research and development to manufacturing and beyond. It highlights the pivotal roles of artificial intelligence (AI), automation, and innovative digital platforms in reshaping every aspect of the pharmaceutical pipeline. The discussion emphasizes how these technologies are transforming the way medicines are discovered, developed, and even manufactured, pushing the boundaries of what's possible in

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17:49

20 - Quality Risk Management: A Proactive Approach...

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/10

Introduce Quality Risk Management (QRM) as a proactive approach to ensuring quality and safety in pharmaceutical and dietary supplement manufacturing. Explore the core principles of QRM, emphasizing the use of scientific knowledge and experience in evaluating risks, and the proportional allocation of resources based on risk level. Understand the four main stages of the risk management process: risk assessment, risk control, risk communication, and risk review. Delve into the three components of risk

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17:41

19 - Materials Management: From Raw Materials to...

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/10

Explore the comprehensive world of materials management within a GMP framework, understanding how it ensures the quality and consistency of pharmaceuticals and dietary supplements. Discover the importance of rigorous supplier qualification, going beyond price to assess reliability, quality commitment, and adherence to specific requirements. Learn how inventory control manages the flow of materials through a facility, preventing mix-ups and ensuring proper storage conditions to avoid contamination

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13:00

18 - Change Control: Managing Modifications...

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/10

Explore the crucial role of change control in maintaining quality and compliance within regulated industries like pharmaceuticals and dietary supplements. Move beyond the perception of change control as mere paperwork, understanding its comprehensive nature in evaluating, approving, and implementing modifications to processes, equipment, or documentation. Learn how risk assessment and impact analysis are used to identify potential hazards and evaluate the effects of changes on product quality,

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12:08

17 - Equipment Qualification: IQ, OQ, PQ (S15E3)

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/10

Uncover the essential process of equipment qualification in ensuring the safety and efficacy of medicines and supplements. Explore the three key stages: Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). Understand how IQ verifies correct installation and adherence to design specifications, including utility connections and material compatibility, while OQ confirms proper equipment function and adherence to operating ranges. Delve into PQ, which

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16:13

16 - Cleaning Validation: Preventing...

From Concept to Medicine - A Comprehensive Drug... ·

2025/05/10

Examine the critical role of cleaning validation in pharmaceutical and dietary supplement manufacturing, focusing on the establishment of robust protocols to prevent cross-contamination. Understand how cleaning validation goes beyond simple cleanliness, ensuring product integrity and compliance with regulatory standards like GMP. Explore the concept of acceptance criteria, defining "clean" in a scientifically rigorous manner and considering factors like toxicity, potency, and detectability of

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270 results

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