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    biosimilars

    Explore " biosimilars" with insightful episodes like "Current Commercial Landscape for Pharma in Canada", "Audio Guide: Biosimilars", "The Next Step with Biosimilars", "Do BioSimilars Need a Patient Support Program?" and "CADTH - Streamlined Input Processes for Patients and Clinicians" from podcasts like ""The Pharma Podcast", "Patient PrepRheum Podcast", "Patient PrepRheum Podcast", "The Pharma Podcast" and "The Pharma Podcast"" and more!

    Episodes (41)

    Current Commercial Landscape for Pharma in Canada

    Current Commercial Landscape for Pharma in Canada

    On this episode of the PharmaPodcast my guest is Michael Cloutier,  founding partner at Accelera Canada.   Mike has been CEO/President/GM of seven Canadian companies and affiliates including: Searle, Pharmacia, AstraZeneca, COTI, InterMune, PTC Therapeutics, Diabetes Canada! 

    Mike and I discuss the current commercial landscape for pharma in Canada, including its challenges and opportunities.

    Contact Information:
    Michael Cloutier
    Founding Partner
    michael.cloutier@acceleracanada.com
    289-208-4191

    210B-219 Dufferin Street,
    Toronto, ON M6K 3J1

    Audio Guide: Biosimilars

    Audio Guide: Biosimilars

    This is an audio guide about biosimilar medications, brought to you by CreakyJoints Australia.

    Be sure to go to CreakyJoints Australia website, and join for free to keep updated on all of our resources.

    TRANSCRIPT

    Audio Guide 1: Biosimilar Medications

     

    This is an audio guide about biosimilar medications, brought to you by CreakyJoints Australia.

    A biosimilar medication (also known as a “biosimilar”) is a very close duplicate of an original brand of biologic medication (or “biologic”). 

    Biologic medications are developed from living cells and are used for a wide range of conditions including diabetes, chronic kidney failure and some types of cancer. They are often also prescribed to treat autoimmune conditions such as rheumatoid arthritis, psoriatic arthritis and Crohn’s disease.

    You might already be using biologics such as etanercept (sold under the brand name Enbrel), infliximab (sold under the brand name Remicade) or adalimumab (sold under the brand name Humira) to help treat your condition.

    Biologics have large complex molecular structures compared to tablet medications. (Picture a basketball next to a pea and you’ll get the idea.) As a result, they cannot be processed through the digestive system. Instead, they are injected or infused into the bloodstream.

    Unlike the synthetically made generic versions of tablet-form medications (which are 100 per cent identical to the original brand-name medication), biosimilars are almost identical copies of biologics.

    Biosimilars are made using the same research and materials as the original reference biologics they replicate. The manufacturing processes are also exactly the same. Biosimilars even have the same active ingredient name as their reference biologic, but they are sold under different brand names.

    However, the end products can never be exactly the same as the original biologics, so they cannot be reproduced identically. Both biologics and biosimilars can even vary slightly between batches.

    Does this mean biosimilars are safe?

    Yes, they are. The very minor differences between a biosimilar and its reference biologic mean that the biosimilar has the same safety profile as the reference biologic. Both must go through the clinical trial process, although biosimilars can use some of the data from the clinical trials conducted for their reference biologic.

    Biosimilars must also pass the same strict regulation processes of Australia’s Therapeutic Goods Administration. Biosimilars will not be approved if they don’t meet the same quality, efficacy and safety standards as their reference biologics.

    Is there a cost difference between biologics and biosimilars?

    While biologics are planned and developed from the ground up, biosimilars are based on biologic structures that already exist. This means they are more cost-effective to produce than their reference biologic so they can be sold to the government at a lower price. 

    Additionally, every time a new biosimilar is launched, the price the PBS pays for ALL equivalent medicines in the category drops. For example, if a new adalimumab biosimilar is approved, the price to the PBS of the reference biologic HUMIRA plus other approved adalimumab biosimilars all drop to the same lower price.

    In the long run, that means less expensive medicine as the cost savings allow the government to invest in other medications and areas of the healthcare system.

    There is no price difference for consumers between biologics and biosimilars as these are sold at the same fixed price through the Pharmaceutical Benefits Scheme (PBS). However, consumers benefit from the increased range of treatment options available to them.

    How are biosimilars prescribed?

    Only rheumatologists and clinical immunologists are authorised to prescribe biologics and biosimilars in Australia. If you have autoimmune arthritis you will most likely see a rheumatologist to access either of these medication types. 

    There are several ways you may be prescribed a biosimilar.

    Firstly, if you meet the access requirements and have not previously been treated with a biologic medication  your rheumatologist may prescribe an appropriate biosimilar for you if there is an approved one on the market for your condition. Also, if you have tried a biologic or biosimilar of one active ingredient and it didn’t work for you, your rheumatologist may prescribe a biosimilar with a different active ingredient that you haven’t tried.

    Second, you may receive a biosimilar brand if you have been treated with an original biologic brand of the same active ingredient (such as etanercept) and it has been successful. Your rheumatologist can simply specify the biosimilar brand name they use on your prescription. (This process is known as “switching”.)

    Finally, just as brands of synthetic medications can be substituted with their generic counterparts at pharmacy level, so too can original brands of biologics be substituted with their equivalent biosimilars without the pharmacist checking with the prescriber. This process is known as ‘A’ flagging. 

    It is important to note that biologics will never be switched for biosimilars at pharmacy level if your rheumatologist has ticked the ‘Brand Substitution not permitted’ box on the prescription form. This ensures your biologic won’t be substituted for its biosimilar unless your rheumatologist deems it safe.

    Studies have shown there are no increased risks to patients switching between biologics and biosimilars of the same type of medication, although it is always best to speak to your rheumatologist about which options are best for you. 

    For more information about biosimilars visit the Arthritis Treatments section of the CreakyJoints Australia website (creakyjoints.org.au/education/arthritis_treatment_options/). If you have any further questions regarding biosimilars and biologics in relation to your treatment, speak to your rheumatologist.

    See omnystudio.com/listener for privacy information.

    The Next Step with Biosimilars

    The Next Step with Biosimilars

    In our premiere episode, we’ll be talking about biologic medicines and biosimilars.  These are medicines that are used to slow or stop the progression of autoimmune arthritis and reduce disease activity when conventional tablet-form medications aren’t working well enough for you. We’ll hear from Ann Laherty-Hunt, a patient who was diagnosed with Rheumatoid Arthritis in 2012 and was a gym junkie before starting to notice sore joints and getting night sweats. Ann shares her treatment journey of trying various DMARD therapies before getting onto biosimilars, which have changed her life. Rheumatologist, Dr David Liew will help us understand the difference between biologics and biosimilars and the safety and efficacy standards that biosimilars must meet before becoming an approved medicine. He also explains the prescribing process of how patients can access biosimilars through the Pharmaceutical Benefits Scheme.

    Dr David Liew Profile
    David Liew is a rheumatologist and clinical pharmacologist at Austin Health in Melbourne and also leads the Medicines Optimisation Service there. He is also the deputy editor of Rheumatology Republic and a co-host of the Australian Prescriber Podcast.

    Amongst other committee positions, he served on the Council of Australian Therapeutic Advisory Groups' Expert Advisory Group for the Guiding Principles for the Governance of Biologics and Their Biosimilars in Australian Hospitals and maintains an academic interest in adverse drug reaction surveillance.

    HOST: Naomi Creek

    PATIENT: Ann Laherty-Hunt

    DOCTOR: Dr David Liew

    When my Rheumatologist spoke to me she said, you’ve got the biologics that I’m sure you’ve heard of, she said but there’s also biosimilars, which are very similar to the biologic.

    Welcome to Patient Prep Rheum, a podcast where we speak to people living with autoimmune arthritis and related conditions, as well as health professionals to fully understand important aspects of living with these conditions. We want to empower patients so they are prepped and ready to be at the centre of their own health and make their disease journey a smooth one.

    Hi, I’m Naomi Creek, the National Coordinator for CreakyJoints Australia, and I have been managing Rheumatoid arthritis since I was 12 years old. The challenges I have faced have made me a passionate advocate for people living with chronic pain. 

    In this episode, we’ll be highlighting two of the main options used to slow or stop the progression of autoimmune arthritis and reduce disease activity when conventional tablet-form medications aren’t working well enough for you.

    These options are biologics and biosimilars.”

    Ann Laherty-Hunt is a nurse that lives in regional Victoria, and was diagnosed with Rheumatoid arthritis in 2012.

    I was being a gym junkie, and my husband and I were going to the gym a lot, and I was getting sore thumb joints, and I went to a physio to get some strapping because I thought it was from overworking the joints, and then I was having night sweats and of course I'm going, well this isn’t right, and started looking into what it could be, and I was diagnosed with Rheumatoid arthritis in December 2012.

    I started on, of course the bog standard methotrexate, so I was on that for a while and then I still didn’t have much control, so then we added in plaquenil, and it was still better but not great, and then eventually we added in the pyralin. With those three I probably got really good control for 18 months to two years.

    After those two years, it looked as though Ann would go into remission, but then her condition spiralled. That is when Ann and her Rheumatologist started talking about another way to treat her condition that they hadn’t yet tried.

    I knew there was the next step. She said you’ve got the biologics that I’m sure you’ve heard of, but there’s also biosimilars. She said it’s not quite the same as a biologic, because it’s a slightly different compound, but it has the same effect.

    So what exactly are the scientific differences between a biologic and a biosimilar? Are they even that different? Rheumatologist and clinical pharmacologist, Dr. David Liew explains

    There are a lot of medications we can just synthetically produce, and we make in a factory and just copy exactly, but some of the most important medicines in Rheumatology are bigger molecules, they’re monoclonal antibodies, just like other antibodies floating around our system.

    They’re big complex biologic things that we just simply can’t copy exactly. Not only are they really big in terms of the coding that makes up them, but they do all sorts of things after they are coded, which means that they fold in different ways, and they get affected in different ways, and basically you can’t copy them exactly.

    A biosimilar is the best attempt to try and be able to replicate that, making sure all of the important bits are replicated, making sure it works in the same way, but with the knowledge that we can never ever copy it.

    By the time a biosimilar gets to you, the consumer, it’s gone through so much of a process to get there.

    Not only does it have to have the same basic makeup, it has to go through the same laboratory tests to make sure it’s exactly the same in the way that it performs, but it has to go through processes in humans where it does exactly the same, not better, not worse, exactly the same.  

    This is something you can hand on heart, say, stacks up against the originator.

    Ann’s rheumatologist discussed the medical differences between biologics and biosimilars, but there were a few other social factors that helped Ann make her decision between choosing a biologic or a biosimilar.

    She also discussed that it’s cheaper for the Government as well because she said that’s why they’ve brought them out, because biologics are very expensive.

    One thing I’ve noticed from a lot of the support groups online is that people really stress about getting their scripts to get their injections. Because I’m rural I was like I don’t want to have to be having that as an extra worry. So I spoke to her about that and she said the good thing about the biosimilars is that they don’t need to have the approval every couple of months.

    Once you get it it’s like 3 months or a year or something, I don’t have to wait for medicare. Even though it’s an injection once a week, I thought I would go with the biosimilar. As long as it works I don’t really care if it’s a biologic or a biosimilar.

    This process that Ann speaks about  is known as streamlined authority. This isn’t available for all biologics and biosimilars, it also doesn’t replace her appointments with her rheumatologist, however it dramatically cuts down her approval time to receive the medication.

    Streamlined authority makes the process for both the patient and the doctor, much simpler.

    That’s that process where every six months on the PB, I or the treating rheumatologist has to sit down with whoever the patient is, and go through and fill out some paperwork, scan it into the system, send it off electronically, wait for someone to manually review it, and then send it back. That’s an arduous process for everyone.

    That’s only there because of the cost effectiveness and variance. We need to make sure that the patients who are getting it, are the ones who are benefitting from it.

    But patients who are going on biosimilars now, get to the process where after the first time it works, they can get a streamlined approval. Which means they leave the rheumatologists office, with a prescription in hand with a streamlined code on it, which is good to go, so they never have to do that waiting.

    Having lived for so many years with chronic pain and ongoing symptoms, Ann said it was an easy decision to try a new medicine with such promise. The rheumatologist confirmed Ann’s eligibility for being prescribed a biosimilar for her rheumatoid arthritis after confirming that enough of her joints were affected by this condition.

    That is a threshold that is set by the Government, which is the same for any biologic, *for rheumatoid arthritis* whether it’s the originator or the biosimilar for rheumatoid arthritis after biologic. Basically the Government wants to see that there’s at least 20 joints affected, or it could be four large joints, like knees or shoulders. That’s a process that applies for normal biologics or biosimilars, and that's really just about making sure that we are using these medications in the patients that are going to benefit the most.

    It was a long and painful process for Ann to finally be prescribed a biosimilar over oral medication. She made the switch 12 months ago and noticed a difference within months.

    The change in my condition has been amazing. The main thing it got rid of was my fatigue, my fatigue is gone. That was the most crippling part of my disease, I felt.

    Within about 2 or 3 months I noticed I wasn’t fatigued anymore. The pain has reduced of course, but the pain you can take a tablet for, the fatigue you can’t do anything for, so I’m wrapped that that’s been the biggest change, for me is just not being tired, for no reason, all the time, and then not being able to sleep. It’s been life changing in that regard.

    As for Rheumatologist and Chemical Pharmacologist, Dr David Liew, biosimilars are a treatment that he actively prescribes for patients who require it.

    I trust biosimilars, I’d happily take a biosimilar and I’d happily change my patients from originators to biosimilars when appropriate.

    Although Ann has had an uphill battle since her diagnosis with Rheumatoid Arthritis, she worked with her Rheumatologist to find the right treatment for her.

    If you want to learn more about biosimilars, listen to our audio guide or find more information at creaky joints.org.au.

    If you are considering how or if biosimilars fit into your treatment plan, speak to your rheumatologist.

    Thanks for listening to this episode of Patient Prep Rheum.

    See omnystudio.com/listener for privacy information.

    Do BioSimilars Need a Patient Support Program?

    Do BioSimilars Need a Patient Support Program?

    On this episode of the Pharma Podcast my guest is Nicole Serena, President and Managing Director at PSPConsult, a division of Waldron & Associates and co-founder of PSPCertify – a new Certification Program for PSP Professionals. 

    Nicole and I discuss BioSimilars and the need for Patient Support Programs to support them.   

    Contact Information:
    Nicole Serena
    President & Managing Director PSPConsult
    A division of Waldron & Associates
    nicole@pspconsult.ca
    www.pspconsult.ca


    CADTH - Streamlined Input Processes for Patients and Clinicians

    CADTH  - Streamlined Input Processes for Patients and Clinicians

    Ryan Clarke is CEO and founder of Advocacy Solutions and a Senior Partner at Accelera Canada, where he is responsible for Advocacy & Stakeholder Relations.

    In this episode of The Pharma Podcast Ryan discusses CADTH (Canadian Agency for Drugs and Technologies in Health)  and the streamlined input processes for both patients and Clinicians.

    Contact Information:
    ryan.clarke@acceleracanada.com

    C: 416.919.9532 
    Toll Free: 1.800.250.1569
    219 Dufferin Street, Unit 210B, Toronto ON, M6K 3J1

     

    PMPRB New Guidelines Affecting Drug Pricing in Canada

    PMPRB New Guidelines Affecting Drug Pricing in Canada

    On this episode of The Pharma Podcast my guest is Lindy Forte, Senior Partner, Health Technology Assessment at Accelera Canada .

    Lindy discusses the Patented Medicines Pricing Review Board (PMPRB),  the amendments to the Patented Medicines Regulations and its impact on Drug prices in Canada.

    She also shares her thoughts on what she likes about the new regulations, and some potential shortcomings.

    This episode of the podcast is a must listen to for any pharma professional considering launching a new drug in Canada.

    Contact Information:
    www.acceleracanada.com
    lindy.forte@acceleracanada.com

    Canadian Attitudes on Healthcare and Telemedicine

    Canadian Attitudes on Healthcare and Telemedicine

    In this episode of the PharmaPodcast my guest is Vijay Wadhawan, Vice President, Health and Wellness at Environics Research.   

    Getting fast, convenient access to healthcare can be frustrating for many Canadians. COVID19 has exacerbated existing challenges. Telemedicine is a new delivery channel for medicine with the potential to make healthcare more accessible.  

    Vijay discusses the findings from a recent survey conducted by Environics Research to understand Canadian attitudes toward healthcare and telemedicine.   

    Contact Information for Vijay Wadhawan:
    linkedin.com/in/vwadhawan
    Vijay.Wadhawan@environics.ca
    https://environicsresearch.com/capabilities-insights/health-wellness/

    Canadian R&D Investment & its Promise in the Wake of COVID-19

    Canadian R&D Investment & its Promise in the Wake of COVID-19

    In this episode of The Pharma Podcast, my guest is Brian Bloom, co-founder and CEO of Bloom Burton.   

    Brian gives us a snap shot of the Canadian R&D landscape, its promise, and how Canadian innovation has been impacted by COVID-19 and how it is contributing to the fight against COVID-19. 

    Brian is a true champion of our industry. To bring any new therapy to market requires a good idea, bright minds and a lot of money.   

    Brian and his team at Bloom Burton have helped a lot of smart people with bright ideas find the money to fund their dreams and bring new therapies to patients.   

    This podcast was  recorded on the heels of the 2020 Bloom Burton Award Gala hosted by Brian and his business partner, and fellow co-founder, Jolyon Burton. The award gala highlights what is possible when we fund smart people with bright ideas. 

    COVID19 Vaccine Distribution in Canada-- Industry Perspective

    COVID19 Vaccine Distribution in Canada-- Industry Perspective

    Several COVID19 vaccine candidates are in development and launch plans are being drafted. 

    Progress is unfolding at an unprecedented pace. More than 200 potential vaccines are in development and more than 40 have entered human trials.  Applications for approval have  already been submitted to Health Canada under the Interim Order. 

    Canada, currently, has access to a guaranteed 174 million doses of potential COVID19 vaccines. This represents over $1 billion in advance purchase agreements  

    Canada has also pledged to the World Health Organisation's Advanced Market Commitment (AMC) $220 million to purchase 15 million vaccine doses from the COVAX facility plus $220 million to purchase doses for low- and middle-income countries. 

    Securing regulatory approval and supply agreements is a great first step, but how will the vaccine be rolled out safely and  equitable as possible?

    To help us understand how industry in Canada is preparing for the roll out, I’ve invited  Daniel Chiasson, President and CEO, of the Canadian Association for Pharmacy Distribution Management (CAPDM). 

    COVID-19 Financial Resources Available to Canadian Pharma

    COVID-19 Financial Resources Available to Canadian Pharma

    In this Episode of The Pharma Podcast  we will discuss the financial resources available to Canadian life science companies facing financial hardship in the wake of the COVID-19 Pandemic. 

    My guest is Dan Juskovic, Head, Life Sciences and Health Services, RBC.  

    Dan offers sound advice  to help  Life Science Companies in Canada who have been directly impacted by COVID-19 and as a result are facing financial challenges.

    Dan can be reached by email at: dan.juskovic@rbc.com

    COVID-19 Special Edition – Canadian Access to Future Coronovirus Treatment – Canadian Regulatory Framework

    COVID-19 Special Edition – Canadian Access to Future Coronovirus Treatment – Canadian Regulatory Framework

    In this episode I spoke with Nathaniel Lipkus, intellectual property litigator, and partner at Osler, Hoskin & Harcourt LLP.

    Nate is a legal expert on patent and regulatory issues facing pharmaceutical and biotechnology companies. 

    Nate has also published extensively on topics pertaining to Canada’s Patent Act . Nate  recently wrote an article for the Globe and Mail exploring today’s topic.   

    In this episode, Nate provides insight on Canada's regulatory framework and how it can assist Canadian access to new therapeutics to the novel coronavirus.  Specifically, we explore the COVID-19 Emergency Response Act (Bill C-13) and its provisions. 

    We also explore Canada’s industrial capability to meet future demand to treatment.

    CONTACT INFORMATION

    nlipkus@osler.com

    The Evolving Role of Specialty Pharmacy in Canada.

    The Evolving Role of Specialty Pharmacy in Canada.

    Jane Farnham is a recognized thought leader in streamlining the complex processes for patients receiving speciality medications. She has both a professional and personal interest in the rare disease space. 

    In this episode, Jane will provide insights on “The evolving role of specialty pharmacy in supporting patients with increasingly complex new therapies in a changing regulatory and reimbursement environment.”

    Contact Information:
    janefarnham8888@gmail.com.

    Market Entry in Canada and the Pitfalls to Avoid - a GM's Perspective.

    Market Entry in Canada and the Pitfalls to Avoid - a GM's Perspective.

    Accelera Canada is Canada’s premier consulting firm offering end to end advice and services to emerging companies wanting to bring their new medical innovation to Canada.  

    Deborah Brown is one of Canada's most experienced General Managers with close to three decades  of industry experience -- both domestic and international.

    In this episode, Deb will share her insights on how to optimize one's approach to planning a market entry in Canada and the commercial options that emerge from that analysis - and the pitfalls to avoid!

    Contact Information:
    www.acceleracanada.com
    deborah.brown@acceleracanada.com.

     

    Ep. 116: Drug Discovery for India

    Ep. 116: Drug Discovery for India

    How is a new drug discovered or invented? What does it take for medicine to go from a small idea in a research lab all the way to your local pharmacy? How can we develop new medicines for India and Indian ailments?

    Pavan Srinath is in the guest seat today as he talks to Anupam Manur, a frequent guest and friend of The Pragati Podcast. He retells the tale of how Penicillin was discovered, and tracks how drug discovery and development has evolved since then.

    Pavan Srinath is a public policy researcher and educator, and also hosts The Thale-Harate Kannada Podcast. He has an academic background in biotechnology and biosciences before working in public policy.

    Anupam Manur is an Assistant Professor and resident economist at The Takshashila Instituion.

    Also read: Medicines in India, For India: https://www.thehindu.com/opinion/op-ed/Medicines-in-India-for-India/article10678328.ece

    If you have any questions or comments, write in to podcast@thinkpragati.com.

    Follow The Pragati Podcast on Instagram: https://instagram.com/pragatipod Follow Pragati on Twitter: https://twitter.com/thinkpragati Follow Pragati on Facebook: https://facebook.com/thinkpragati

    Subscribe & listen to The Pragati Podcast on iTunesSaavn , Spotify , CastboxGoogle Podcasts , YouTube or any other podcast app. We are there everywhere.

    You can listen to this show and other awesome shows on the IVM Podcasts app on Android: https://ivm.today/android or iOS: https://ivm.today/ios, or any other podcast app.

    You can check out our website at http://www.ivmpodcasts.com/

    See omnystudio.com/listener for privacy information.

    ಮದ್ದುಗಳ ಮೂಲ. Medicines for India.

    ಮದ್ದುಗಳ ಮೂಲ. Medicines for India.

    ಔಷಧಿಗಳನ್ನು ಹೇಗೆ ಕಂಡುಹಿಡಿಯುತ್ತಾರೆ? ಒಂದು ಹೊಚ್ಚಹೊಸ ಔಷಧಿಯು ಸಂಶೋಧನೆಯಿಂದ, ಮೆಡಿಕಲ್ ಶಾಪ್ ವರೆಗು ಬರುವಾಗ ಯಾವ ಯಾವ ಹಂತಗಳಿಂದ ಹೋಗುತ್ತದೆ? ಭಾರತದಲ್ಲಿ ಹೊಸ ಔಷಧಿ ಕಂಡುಹಿಡಿಯುವುದು ಹೇಗೆ? ಈ ಸಂಚಿಕೆಯಲ್ಲಿ ನಮ್ಮವರೇ ಆದ ಪವನ್ ಶ್ರೀನಾಥ್ ಮತ್ತು ಸೂರ್ಯ ಪ್ರಕಾಶ್ ಅವರು ಔಷಧಿಗಳ ಬಗ್ಗೆ ಚರ್ಚೆ ಮಾಡುತ್ತಾರೆ.

    How is a new drug discovered or invented? What does it take for medicine to go from a small idea in a research lab all the way to your local pharmacy? How can we develop new medicines for India and Indian ailments? Our very own Pavan Srinath talks to Surya Prakash BS about drug discovery and 21st century medicine for Indians.

    Pavan Srinath is a public policy researcher and educator, and also hosts The Pragati Podcast in English. He has an academic background in biotechnology and biosciences before working in public policy.

    Also read: Medicines in India, For India: https://www.thehindu.com/opinion/op-ed/Medicines-in-India-for-India/article10678328.ece

    ಫಾಲೋ ಮಾಡಿ. Follow the Thalé-Haraté Kannada Podcast @haratepod.

    Facebook: https://facebook.com/HaratePod/ Twitter: https://twitter.com/HaratePod/ Instagram: https://instagram.com/haratepod/

    ಈಮೇಲ್ ಕಳಿಸಿ, send us an email at haratepod@gmail.com.

    Subscribe & listen to the podcast on iTunesGoogle PodcastsCastboxAudioBoomYouTubeSouncloudSpotify, Saavn or any other podcast app. We are there everywhere. ಬನ್ನಿ ಕೇಳಿ! 

    You can listen to this show and other awesome shows on the IVM Podcasts app on Android: https://ivm.today/android or iOS: https://ivm.today/ios, or any other podcast app.

    You can check out our website at http://www.ivmpodcasts.com/

    See omnystudio.com/listener for privacy information.

    Data Integrity and Quality Culture

    Data Integrity and Quality Culture

    In this episode of RCA Radio, host Erika Porcelli and guest Susan Schniepp, Distinguished Fellow at Regulatory Compliance Associates (RCA), examine the resurgence of data integrity issues and the focus of global regulatory agencies. With the recent rise in data integrity-related citations, global regulatory bodies including the FDA, MHRA, World Health Organization, and PIC/S, have released documents to reeducate the pharmaceutical industry on data integrity concepts. Many of these guidelines include an element of quality culture.

    We break down these guidelines and examine the history of data integrity, what it means to have a quality culture, and how to integrate a quality culture in the product lifecycle. No longer just the concern of the quality control unit, data integrity is the concern of an entire organization, bringing forth the concept that your data is only as good as the culture of your company.

    #46: Breakthroughs in Cancer Research with Dr. David Hong Part 2

    #46: Breakthroughs in Cancer Research with Dr. David Hong Part 2

    In today’s episode, John returns to his conversation with renowned cancer researcher Dr. David S. Hong. Dr. Hong is deputy chair of Investigational Cancer Therapeutics at The University of Texas MD Anderson Cancer Center. He also serves as associate vice president for Clinical Research and clinical medical director of the Clinical Center for Targeted Therapy. Dr. Hong has published more than 270 papers in leading academic journals.

    Topics include:

    • Go/No-go decisions in clinical trials.
    • Interchangeability of oncology drugs and biosimilars.
    • Rising drug prices and declining trust in pharmaceutical companies.
    • Health care delivery in the United States.

    Speaker Bios
    Dr. David S. Hong is deputy chair of Investigational Cancer Therapeutics at The University of Texas MD Anderson Cancer Center. He also serves as associate vice president for Clinical Research and clinical medical director of the Clinical Center for Targeted Therapy. Dr. Hong received a bachelor’s degree in biology from Yale University and a medical degree from Albert Einstein College of Medicine. He then completed an internship and residency at Thomas Jefferson University Hospital and a medical oncology fellowship at MD Anderson, during which time he was appointed chief medical oncology fellow. In 2005, he joined MD Anderson’s faculty.

    Dr. Hong is the recipient of the 2004 Young Investigator Award from the American Society of Clinical Oncology, the Jesse H. Jones Fellowship in Cancer Education, MD Anderson’s Best Boss Award, the Irwin H. Krakoff Award for Excellence in Clinical Research, the Gerald P. Bodey Award for Excellence in Education and a research training fellowship from Howard Hughes Medical Institute. He has published more than 270 articles in prestigious journals.

    John Marchica is a veteran health care strategist and CEO of Darwin Research Group, a health care market intelligence firm specializing in health care delivery systems. He’s a two-time health care entrepreneur, and his first company, FaxWatch, was listed twice on the Inc. 500 list of fastest growing American companies. John is the author of The Accountable Organization and has advised senior management on strategy and organizational change for more than a decade. John did his undergraduate work in economics at Knox College, has an MBA and M.A. in public policy from the University of Chicago, and completed his Ph.D. coursework at The Dartmouth Institute. He is a faculty associate in the W.P. Carey School of Business and the College of Health Solutions at Arizona State University, and is an active member of the American College of Healthcare Executives.

    About Darwin Research Group
    Darwin Research Group Inc. provides advanced market intelligence and in-depth customer insights to health care executives, with a strategic focus on health care delivery systems and the global shift toward value-based care. Darwin’s client list includes forward-thinking biopharmaceutical and medical device companies, as well as health care providers, private equity, and venture capital firms. The company was founded in 2010 as Darwin Advisory Partners, LLC and is headquartered in Scottsdale, Ariz. with a satellite office in Princeton, N.J.

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