AI For Pharma Growth

Dr Andree Bates

AI For Pharma Growth is the podcast from pioneering Artificial Intelligence entrepreneur Dr. Andree Bates created to help Pharma, Biotech and other Healthcare companies understand how the use of AI-based technologies can easily save them time and grow their brands and company results. This show blends deep experience in the sector with demystifying AI for biopharma execs from biotech start-ups right through to big pharma. In this podcast, Dr Andree will teach you the tried and true secrets to building results in a pharma company using AI and alert you to some fascinating new tools and applications to benefit you and your company. As the author of many peer-reviewed journals in pharma AI, and having addressed over 500 industry conferences across the globe, Dr Andree Bates uses her obsession with all things AI, futuretech, healthcare and pharma to help you to navigate through the, sometimes confusing, but magical world of AI powered tools to achieve real-world results. This podcast features many experts who have developed powerful AI-powered tools that are the secret behind some time-saving and supercharged revenue-generating business results. Those who share their stories and expertise show how AI can be applied to Discovery, R&D, clinical trials, market access, medical affairs, regulatory, market research, business insights, sales, marketing, including digital marketing, and so much more.

  1. E216: When AI meets Cell Engineering

    4 DAYS AGO

    E216: When AI meets Cell Engineering

    Cell therapies have huge potential, but cost, complexity, and centralised manufacturing have kept many of them confined to last-line use. In this episode, Dr Andree Bates speaks with Armon Sharei, Founder and CEO of Portal Biotechnologies, about what happens when AI meets cell engineering, and why point-of-care delivery could make personalised cell programming more practical, scalable, and safer. Armon explains Portal’s core idea: cells are programmable machines. If you can reliably deliver multiple cargoes into cells, you can instruct new behaviours. Portal’s method briefly “squishes” cells through precision pores to disrupt the membrane so external material can enter, opening the door to complex cell engineering without permanent genome edits. They explore where AI fits in: modelling cell behaviour. By combining perturbation experiments, rich readouts, and phenotypic screening, AI can help generate “virtual cell models” that suggest which RNA instructions to deliver to drive specific outcomes. The bottleneck is data at the right complexity, because many effects only appear when multiple pathways are changed at once. A key takeaway is the safety and flexibility of transient RNA reprogramming. Unlike irreversible genetic modification, RNA fades within days, reducing long-term risk and making earlier-line use more realistic. Armon also discusses how point-of-care workflows may be regulated differently, with the machine treated as a device and the cargo as the drug. Looking ahead, he paints a vision of infusion-centre cell programming: a compact system that takes blood, delivers tailored RNA instructions to immune cells, and returns them within hours, potentially bringing costs closer to mainstream biologics and expanding access. Topics Covered Why delivery is the unlock for programmable cell therapiesHow Portal’s “cell squishing” delivery worksUsing AI to model cells and generate functional programmesThe data bottleneck and why multi-perturbation datasets matterPhenotypic screening and lab-to-clinic feedback loopsTransient RNA reprogramming vs permanent genetic modificationRegulatory implications of point-of-care engineeringEconomics and scalability of point-of-care approachesNear-term opportunities in oncology and autoimmunityThe future vision for infusion-centre personalised therapiesEularis helps pharma and biotech leaders turn AI activity into board-defensible strategy and measurable commercial outcomes. If your organisation has plenty of AI in motion but very little that moves the commercial needle in a way the board can see, start with our 10-Day AI Diagnostic Sprint. It’s a focused diagnostic that surfaces what’s actually broken and what’s blocking results, before you invest in a larger strategy effort. The Sprint diagnoses the problem. The AI Strategic Blueprint that follows is where we build the board-defensible strategy and plan.Details at eularis.com. About the Podcast AI For Pharma Growth is the podcast from pioneering Pharma Artificial Intelligence entrepreneur Dr Andree Bates, created to help pharma, biotech and healthcare organisations understand how AI-based technologies can save time, grow brands, and improve company results.This show blends deep sector experience with practical conversations that demystify AI for biopharma leaders, from start-up biotech right through to Big Pharma. Each episode features experts building AI-powered tools that are driving real-world results across discovery, R&D, clinical trials, medical affairs, market access, regulatory, insights, sales, marketing, and more. AI platforms and tools solve specific problems. Strategy makes sure you’re solving the right ones, in the right order. If you want help mapping priorities as you evaluate what to roll out next, send me a LinkedIn DM starting with ‘PRIORITIES’ and two lines: what’s already in flight, and the decision you’re trying to make next. Dr. Andree Bates LinkedIn | Facebook | X

    31 min
  2. E215: Location, Location, Innovation: AI Site Twins and the New Era of Site Selection

    28 APR

    E215: Location, Location, Innovation: AI Site Twins and the New Era of Site Selection

    Clinical trial site selection is one of the biggest hidden bottlenecks in drug development, and it’s still often driven by legacy relationships, spreadsheets, and habit. In this episode, Dr Andree Bates interviews Simon Arkell, founder of Ryght, Inc, about “AI Site Twins” and why the next era of site selection shifts from institutional memory to predictive, real-time analytics. Simon explains why the current model produces terrible outcomes at scale: too many activated sites under-enrol, competition at sites is poorly understood, and sponsors often don’t see the failure until timelines have already slipped. He argues this is primarily a site selection problem, because “the easy button” of re-using familiar sites reduces data-driven decision making, even as trials get more complex and patient competition intensifies. Ryght’s approach is to build AI-powered digital replicas of research sites, creating a unique identifier and a dynamic “twin” profile that continuously improves as new data arrives. Simon walks through how protocols can be matched to sites across countries, then enriched using harmonised public data, competitive trial context, and automated outreach that dramatically increases engagement. He also describes how different AI agents help fill missing information, find the right contacts, and capture context across email, portals, and voice interactions to improve future matching. The upside is massive: faster feasibility, better site choices, shorter time-to-activation, earlier first-patient-in, and ultimately faster time-to-market. Simon links these operational gains to commercial reality: every month saved can mean earlier revenue, longer effective patent runway, and more lives impacted by getting therapies to patients sooner. Topics Covered Why site selection is still a major bottleneck in clinical trials The true cost of underperforming sites and enrolment failure What an AI Site Twin is and how it differs from legacy databases Global protocol-to-site matching and competitive trial context Data harmonisation from messy public sources Agent workflows: enrichment, outreach, contact finding, and context capture Engagement rates and accelerating feasibility timelines Enrolment curve modelling and predicting site performance Security, HIPAA/GDPR compliance, and sponsor data integration Time-to-activation, first-patient-in, and time-to-last-patient-in KPIs Why “execution speed” and flywheels create a moat in AI applications Eularis helps pharma and biotech leaders turn AI activity into board-defensible strategy and measurable commercial outcomes. If your organisation has plenty of AI in motion but very little that moves the commercial needle in a way the board can see, start with our 10-Day AI Diagnostic Sprint. It’s a focused diagnostic that surfaces what’s actually broken and what’s blocking results, before you invest in a larger strategy effort. The Sprint diagnoses the problem. The AI Strategic Blueprint that follows is where we build the board-defensible strategy and plan.Details at eularis.com. About the Podcast AI For Pharma Growth is the podcast from pioneering Pharma Artificial Intelligence entrepreneur Dr Andree Bates, created to help pharma, biotech and healthcare organisations understand how AI-based technologies can save time, grow brands, and improve company results.This show blends deep sector experience with practical conversations that demystify AI for biopharma leaders, from start-up biotech right through to Big Pharma. Each episode features experts building AI-powered tools that are driving real-world results across discovery, R&D, clinical trials, medical affairs, market access, regulatory, insights, sales, marketing, and more.

    35 min
  3. E214: Beyond Copilot

    21 APR

    E214: Beyond Copilot

    For many life sciences teams, the first wave of AI has looked like copilots: smart search, quick answers, and help on demand. Useful, but passive. In this episode, Dr Andree Bates is joined by Parth Khanna, CEO and co-founder of ACTO, to explore what comes next: moving beyond copilots into role-based AI agents that proactively close knowledge gaps, improve field readiness, and operate safely inside regulated environments. Parth shares his path into life sciences and tech, including founding an early NLP company in 2012 and then building ACTO after speaking with over 100 life science companies about field force effectiveness. Today, ACTO supports tens of thousands of professionals and hundreds of brand launches, and Parth argues the industry is now entering the “agentic era” where the real differentiator is not just model access, but how organisations build context, control, and change management around AI. A key theme is why generic AI tools often fail inside enterprises. Parth outlines four requirements for agent success: context (role and job-specific personalisation), connection (stitching data sources and agent-to-agent workflows), control (testing, monitoring, observability), and change management (reducing fear and driving adoption). Without these, he says, many copilots and assistants end up underused, with people quietly reverting to old workflows. Parth then introduces ACTO’s concept of role-based “super agents”, designed around a real job description (for example an MSL). Rather than a disconnected swarm of task bots, a “queen bee” orchestrator agent delegates to worker agents, checks outputs against compliance guardrails, and can be assessed with exams to quantify risk before deployment. This approach, he argues, makes AI both more powerful and safer for regulated field teams. Finally, the conversation looks ahead. Parth believes the future of work depends on pairing AI capability with distinctly human strengths: strategy, judgement, and human connection. The winners won’t be those who automate the most tasks, but those who redesign roles so humans and agents amplify each other. Topics Covered Why copilots are useful but fundamentally passive The shift from AI that responds to AI that acts Why generic tools fail: context, connection, control, change management Adoption reality: why many AI assistants go unused Quantifying risk and moving from black box to observable AI Role-based super agents and the “queen bee” orchestrator model Testing agents with exams before field deployment Guardrails, compliance, and agent-to-agent quality checks Human skills AI can’t replace: strategy, judgement, connection The future of MSL and field excellence in an agentic era Eularis helps pharma and biotech leaders turn AI activity into board-defensible strategy and measurable commercial outcomes. If your organisation has plenty of AI in motion but very little that moves the commercial needle in a way the board can see, start with our 10-Day AI Diagnostic Sprint. It’s a focused diagnostic that surfaces what’s actually broken and what’s blocking results, before you invest in a larger strategy effort. The Sprint diagnoses the problem. The AI Strategic Blueprint that follows is where we build the board-defensible strategy and plan. Details at eularis.com. About the Podcast AI For Pharma Growth is the podcast from pioneering Pharma Artificial Intelligence entrepreneur Dr Andree Bates, created to help pharma, biotech and healthcare organisations understand how AI-based technologies can save time, grow brands, and improve company results. This show blends deep sector experience with practical conversations that demystify AI for biopharma leaders, from start-up biotech right through to Big Pharma. Each episode features experts building AI-powered tools that are driving real-world results across discovery, R&D, clinical trials, medical affairs, market access, regulatory, insights, sales, marketing, and more.

    39 min
  4. E213: The Diagnostic Room: We have AI initiatives, but do we have a strategy? The quickest self-test

    14 APR

    E213: The Diagnostic Room: We have AI initiatives, but do we have a strategy? The quickest self-test

    Many pharma and life science organisations have been investing in AI for years: pilots across commercial, medical, regulatory, and R&D, innovation labs, steering committees, vendor spend, and genuine effort from smart teams. And yet the same story keeps showing up in boardrooms: ROI is unclear, adoption is patchy, and leaders struggle to explain how all the AI activity connects to strategic goals. In this solo episode, Dr Andree Bates steps into “The Diagnostic Room” to explain why this happens, and why it’s usually not a technology, talent, or speed issue. It’s a diagnosis issue: organisations often haven’t identified what is actually constraining value, so they end up executing hard on the wrong problem. Dr Andree shares a real example from a mid-sized pharma company that believed its AI programme was failing due to lack of velocity. On the surface, it was a reasonable hypothesis. But a focused diagnostic revealed three hidden structural blockers: unclear decision rights for scaling pilots into production, fragmented data ownership preventing access to the best datasets, and incentive misalignment where the people expected to adopt AI tools were not rewarded for the behaviours those tools required. She then clarifies what a diagnostic is and is not. A diagnostic is not a strategy, roadmap, vendor shortlist, financial model, or implementation plan. Instead, it provides evidence-based clarity: what’s broken, how you compare to peers, what’s at stake, and what questions have been opened that cannot responsibly be answered in ten days. That clarity creates a shared language for leadership, replacing vague frustration with a precise problem statement. The organisations pulling ahead are not simply those with the biggest budgets, but those willing to find what’s actually broken before trying to fix it. Topics Covered Why AI initiatives can grow without creating measurable ROI The gap between pilots and a true AI strategy Misdiagnosis: executing brilliantly on the wrong problem What a diagnostic sprint is (and what it is not) Three hidden blockers Why working groups can’t fix structural AI constraints What a full strategic AI blueprint includes Why many AI business cases are untested projections How to improve board confidence with evidence, governance, and measurement Why diagnostics create speed by creating shared clarity Eularis helps pharma and biotech leaders turn AI activity into board-defensible strategy and measurable commercial outcomes. If your organisation has plenty of AI in motion but very little that moves the commercial needle in a way the board can see, start with our 10-Day AI Diagnostic Sprint. It’s a focused diagnostic that surfaces what’s actually broken and what’s blocking results, before you invest in a larger strategy effort. The Sprint diagnoses the problem. The AI Strategic Blueprint that follows is where we build the board-defensible strategy and plan. Details at eularis.com. About the Podcast AI For Pharma Growth is the podcast from pioneering Pharma Artificial Intelligence entrepreneur Dr Andree Bates, created to help pharma, biotech and healthcare organisations understand how AI-based technologies can save time, grow brands, and improve company results. This show blends deep sector experience with practical conversations that demystify AI for biopharma leaders, from start-up biotech right through to Big Pharma. Each episode features experts building AI-powered tools that are driving real-world results across discovery, R&D, clinical trials, medical affairs, market access, regulatory, insights, sales, marketing, and more. If this episode described your situation, send me a LinkedIn DM starting with ‘SENSECHECK’ and two things: the question you’re trying to answer internally, and what’s currently in flight. I’ll reply with what I’d need to see to turn that activity into a defensible plan, and the next step. Dr. Andree Bates LinkedIn | Facebook | X

    27 min
  5. E212: The Ethics of AI

    7 APR

    E212: The Ethics of AI

    AI ethics has moved from theory to urgent necessity, especially as AI systems become embedded in healthcare, business decisions, and society at large. In this episode, Dr Andree Bates is joined by Dr Nadia Morozova, founder of Enriched Insights, to unpack what ethical AI really means in practice, and how organisations can innovate quickly without creating risk, bias, or governance failures. Nadia shares insights from the global conversation on AI ethics, including discussions at Davos, and explains why trust is becoming the true competitive advantage. She argues that organisations should use AI to build stronger, more open relationships with customers and stakeholders, where technology acts as an enabler rather than the centrepiece. The conversation then gets practical. Nadia outlines a human-centric framework for high-quality AI outcomes, covering accurate sampling, futureproofing (because models are trained on the past), data connectivity across sources, and responsible blending of human and synthetic data. She warns that leadership teams often treat AI as “magic”, assuming tools will solve complex problems like data harmonisation without the hard work of ontology, governance, and expert oversight. A real-world example brings this to life: the Zillow case, where initial success collapsed as market dynamics shifted and the model failed to adapt in time, leading to huge losses. For Nadia, the lesson is clear: ethical responsibility is not a checkbox at launch, it requires ongoing monitoring, review, and culture change. Nadia closes with a strategic message for leaders: start with business goals and targeted use cases, involve data experts early, build governance upfront, and keep humans in the loop throughout the AI lifecycle. Done properly, ethical AI is not a constraint on innovation, it is how you protect long-term value and trust. Topics Covered Why AI ethics is now an urgent business and societal issue Trust, transparency, and accountability in AI deployment Human centricity as the foundation of high data quality Accurate sampling and avoiding “biased reality” in models Why futureproofing matters when algorithms learn from the past Data connectivity, governance, and the ontology problem Responsible blending of human and synthetic data Dangerous leadership assumptions about AI “magic” The Zillow case and what happens without ongoing oversight Strategy first: KPIs, targeted use cases, and right-sized models Skills gaps: technical roles, business acumen, and cross-functional teams Culture change and post-deployment monitoring About the Podcast AI For Pharma Growth is the podcast from pioneering Pharma Artificial Intelligence entrepreneur Dr Andree Bates, created to help pharma, biotech and healthcare organisations understand how AI-based technologies can save time, grow brands, and improve company results. This show blends deep sector experience with practical conversations that demystify AI for biopharma leaders, from start-up biotech right through to Big Pharma. Each episode features experts building AI-powered tools that are driving real-world results across discovery, R&D, clinical trials, medical affairs, market access, regulatory, insights, sales, marketing, and more. Dr. Andree Bates LinkedIn | Facebook | X

    18 min
  6. E211: Precision Monitoring: How Digital Biomarkers Are Changing Medicine

    31 MAR

    E211: Precision Monitoring: How Digital Biomarkers Are Changing Medicine

    Digital biomarkers are turning everyday movement into clinically useful data, giving doctors a clearer picture of what’s happening between appointments, and giving pharma new ways to measure drug impact earlier and more precisely. In this episode, Dr Andree Bates interviews Dr Quique Llaudet, CEO and co-founder of Ephion Health, about precision monitoring and how AI-driven mobility analysis is changing both clinical care and drug development. Quique shares his journey from academic research into entrepreneurship, driven by a desire to turn science into real products that help patients. Ephion Health grew out of early work with paediatric hospitals in Barcelona, where sensor technology used in rehabilitation and exoskeleton projects revealed a bigger opportunity: objective, high-sensitivity gait and movement analysis that can detect disease signatures and track progression over time. The conversation breaks down what a digital biomarker actually is: a measurable signal of health captured via connected devices and analysed with digital methods. Ephion’s platform integrates multiple validated, off-the-shelf sensors to capture rich movement data in a short test, replacing blunt measures like the six-minute walk test with something both more sensitive and less stressful for patients. The system then combines key parameters into a single composite score to track progression and treatment response. Quique also tackles the “black box” concern head on. He explains how their models are developed alongside clinicians, with clinical relevance checked throughout, and how doctors can inspect the underlying parameters behind the biomarker score in a dashboard. For rare diseases with limited data, he highlights deep collaboration with clinicians and patient associations, and the use of synthetic data to support modelling and testing. Finally, Quique outlines the economics: reducing specialist assessment time, enabling more frequent remote monitoring, supporting earlier treatment adjustments, and helping pharma generate evidence in real-world settings. The long-term vision is continuous monitoring that helps clinicians act earlier, plus AI-assisted diagnosis and eventually prevention. Topics Covered What digital biomarkers are and how they differ from traditional biomarkers Turning mobility data into clinically meaningful signals Multi-sensor monitoring: IMUs, pressure insoles, and EMG Why short tests can beat the six-minute walk test Composite biomarker scoring and tracking treatment response AI patterns clinicians may sense but cannot quantify Explainability and building models “hand in hand” with doctors Data challenges in rare disease and the role of patient associations Synthetic data for modelling and validation Economic impact: time savings, remote monitoring, and better treatment adjustment Pharma use cases: real-world evidence and earlier efficacy signals in trials About the PodcastAI For Pharma Growth is the podcast from pioneering Pharma Artificial Intelligence entrepreneur Dr Andree Bates, created to help pharma, biotech and healthcare organisations understand how AI-based technologies can save time, grow brands, and improve company results. This show blends deep sector experience with practical conversations that demystify AI for biopharma leaders, from start-up biotech right through to Big Pharma. Each episode features experts building AI-powered tools that are driving real-world results across discovery, R&D, clinical trials, medical affairs, market access, regulatory, insights, sales, marketing, and more. Dr. Andree Bates LinkedIn | Facebook | X

    33 min
  7. E210: Beyond Alzheimer’s: Scaling Digital Twins Across Disease Areas

    25 MAR

    E210: Beyond Alzheimer’s: Scaling Digital Twins Across Disease Areas

    Digital twins have become one of the most promising tools in Alzheimer’s research, but the bigger story is what happens when they scale across disease areas. In this episode, Dr Andree Bates interviews Aaron Smith, Founder and Head of Machine Learning at Unlearn AI, about how “digital twin generators” can transform trial design by modelling realistic patient progression and improving statistical power without compromising the fundamentals of randomised controlled trials. Aaron shares his journey from academic mathematics into computer vision and machine learning, then into biopharma, where Unlearn began by building generative models that learn the joint distribution of clinical variables. In practice, that means the model can take baseline patient measurements and generate likely future progressions that are as indistinguishable from real clinical records as possible. The conversation dives into a key misconception: digital twins are not only about replacing control arms. Aaron explains a regulatory friendly approach where you keep standard trial structure, but add counterfactual information for every patient into the analysis. Unlearn’s best known method, ProCOVA (prognostic covariate adjustment), summarises a predicted control outcome per patient and uses it for covariate adjustment, creating more efficient treatment effect estimates. The headline result is simple: you can increase power, or reduce recruitment burden while maintaining power, potentially speeding time to results. Finally, Aaron explains why scaling across diseases is genuinely hard. Data structures differ wildly by indication, missingness can block transfer learning, and areas like oncology require modelling complex treatment histories. He also highlights that combining sources is not just “more data”, it demands careful harmonisation and context modelling to avoid biased predictions, especially when bringing in real world evidence. Topics Covered What “digital twin generators” are in clinical trials Generative modelling of clinical records and disease progression Counterfactual prediction under standard of care Why replacing control arms is not the only use case ProCOVA and prognostic covariate adjustment Getting more statistical power and reducing trial size FDA openness to digital twins in trials and what it enables Why scaling across disease areas is not just parameter tuning Missing data, confounding context, and data harmonisation CNS versus oncology modelling challenges Real world evidence and how to validate digital twin models About the Podcast AI For Pharma Growth is the podcast from pioneering Pharma Artificial Intelligence entrepreneur Dr Andree Bates, created to help pharma, biotech and healthcare organisations understand how AI-based technologies can save time, grow brands, and improve company results. This show blends deep sector experience with practical conversations that demystify AI for biopharma leaders, from start-up biotech right through to Big Pharma. Each episode features experts building AI-powered tools that are driving real-world results across discovery, R&D, clinical trials, medical affairs, market access, regulatory, insights, sales, marketing, and more. Dr. Andree Bates LinkedIn | Facebook | X

    32 min
  8. E209: Beyond Failure Prevention: How AI is Redesigning the Drug Discovery Pipeline

    18 MAR

    E209: Beyond Failure Prevention: How AI is Redesigning the Drug Discovery Pipeline

    AI in drug development is moving beyond “failure prevention” into something much bigger: redesigning how we discover, develop, and deliver medicines. In this episode, Dr Andree Bates speaks with Vitalay Fomin of Numenos about biomarker discovery, patient stratification, and why the next breakthroughs come from breaking down data silos across diseases, modalities, and even species. Vitalay shares his background across biotech and pharma, including work in biomarker discovery, translational medicine, and data science, and how frustration with existing approaches led her to build a new architecture for clinical genomic insights. A core theme is that traditional methods often oversimplify biology by forcing outcomes into binary labels and treating each disease area as an isolated box, even when the available data is too limited to answer meaningful questions well. The conversation explores how foundation model approaches can unify clinical, genomic, transcriptomic, proteomic and imaging signals to create a fuller “biological fingerprint” of each patient. Vitalay explains how this can enable earlier insight from single-arm trials by effectively benchmarking against standard-of-care cohorts, helping teams enrich later-stage trials with the right subpopulations sooner, and reducing time and cost. They also discuss the real blockers to adoption: not only scientific conservatism, but commercial uncertainty around how Big Pharma structures deals with tech-bio companies that bring platforms rather than single assets. Vitalay argues that explainability is non-negotiable in this space, because clinicians, scientists, patients, and regulators will not trust black-box predictions. Topics Covered Why AI is shifting from failure prevention to pipeline redesign Biomarker discovery beyond binary responder vs non-responder labels Breaking disease silos to learn across indications Multimodal integration: DNA, RNA, protein, imaging, and clinical data Using foundation models to bridge trial data and real-world data Patient stratification and trial enrichment from early studies Reverse translation and identifying unmet need before target hunting Explainability, trust, and regulatory readiness Adoption barriers: culture, champions, and deal structures for tech-bio Misconceptions about AI in drug development and why “press a button” is a myth About the Podcast AI For Pharma Growth is the podcast from pioneering Pharma Artificial Intelligence entrepreneur Dr Andree Bates, created to help pharma, biotech and healthcare organisations understand how AI-based technologies can save time, grow brands, and improve company results. This show blends deep sector experience with practical conversations that demystify AI for biopharma leaders, from start-up biotech right through to Big Pharma. Each episode features experts building AI-powered tools that are driving real-world results across discovery, R&D, clinical trials, medical affairs, market access, regulatory, insights, sales, marketing, and more. Dr. Andree Bates LinkedIn | Facebook | X

    47 min
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About

AI For Pharma Growth is the podcast from pioneering Artificial Intelligence entrepreneur Dr. Andree Bates created to help Pharma, Biotech and other Healthcare companies understand how the use of AI-based technologies can easily save them time and grow their brands and company results. This show blends deep experience in the sector with demystifying AI for biopharma execs from biotech start-ups right through to big pharma. In this podcast, Dr Andree will teach you the tried and true secrets to building results in a pharma company using AI and alert you to some fascinating new tools and applications to benefit you and your company. As the author of many peer-reviewed journals in pharma AI, and having addressed over 500 industry conferences across the globe, Dr Andree Bates uses her obsession with all things AI, futuretech, healthcare and pharma to help you to navigate through the, sometimes confusing, but magical world of AI powered tools to achieve real-world results. This podcast features many experts who have developed powerful AI-powered tools that are the secret behind some time-saving and supercharged revenue-generating business results. Those who share their stories and expertise show how AI can be applied to Discovery, R&D, clinical trials, market access, medical affairs, regulatory, market research, business insights, sales, marketing, including digital marketing, and so much more.

Information

  • Creator
    Dr Andree Bates
  • Years Active
    2022 - 2026
  • Episodes
    218
  • Rating
    Clean
  • Copyright
    © Dr Andree Bates
  • Show Website
    AI For Pharma Growth

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