Experts from Informa’s Medtrack, Trialtrove and Strategic Transactions teams presented a panel discussion at the recent T3 Conference in Orlando, Florida.
Your fast-pass to the news, insights, and storylines you need to know.
Watch the full webinar here http://ow.ly/4mOGmk
Hosted by Master of Ceremonies Ian Lloyd, senior director of Pharmaprojects and data integration, this webinar spotlights the blockbuster trends and rising stars of global R&D 2016 as seen in this year’s Annual Review.
During this presentation, Ian Lloyd & Scrip Managing Editor, Alex Shimmings cover:
>> Year-on-year growth
>> Clinical phases trends
>> Top companies and the shape of the industry
>> Mergers and acquisitions
>> Trending therapies, diseases, drug types and delivery routes
>> Mechanisms and drug targets
This webinar is the essential pharma R&D trend and forecast overview you need to be positioned for success in 2016.
Watch the full webinar here http://ow.ly/4mOGmk
Analyzing ASCO 2016: Developments, takeaways, and implications from the confe...Pharma Intelligence
In conjunction with a Key Opinion Leader, Dr. Peter Lee MD Chair, Department of Immuno-Oncology at City of Hope Comprehensive Cancer Center, CA, several Informa analysts discuss the major developments of the conference and key take-aways via a Webinar.
Watch our recording of Biomedtracker's Robert Jeng, Ph,D., Citeline's Allison Bruce, Scrip's Mary Jo Laffler, and Datamonitor Healthcare's Zachary McLellan as they download and debrief following the always-exciting ASCO weekend.
View and listen to the full webinar here https://www.youtube.com/watch?v=7yMsCb3R5X8
Over 350 million people worldwide are suffering from rare diseases. Which is why it is necessary to understand the rare disease landscape to date.
Drug development is challenging at the best of times, and made even harder within the realm of rare diseases. Overall, the largest number of drugs has targeted indications within the therapeutic areas of oncology and infectious disease (ID), with malaria being an area of high interest with both therapeutic and preventive interventions.
View this slideshare to get the most accurate and timely intelligence about rare diseases drug development.
In this detailed 20-page report, containing numerous comparative graphs, you will discover:
- The top 25 Rare Diseases by total drugs in development to date
- Current Rare Disease drug development landscape
- Top 15 originators of drugs in development for Rare Diseases (includes non-rare disease drug counts and % of portfolio dedicated to Rare Diseases)
- Therapeutic area distribution of rare diseases and drugs in development
- The top 5 Rare Diseases by drug count per therapeutic area (TA)
- Rare Infectious Diseases with 10 or more drugs in development
- The top 15 originators developing drugs for Rare Infectious Diseases
- Rare cancers with 10 or more drugs in development
- The top 15 originators developing drugs for rare cancers
- Non-ID, non-cancer Rare Diseases with 20 or more drugs in development
- The top 15 originators developing drugs for non-ID, non-cancer Rare Diseases
Complementary Tests and Companion Diagnostics in OncologyDr. Sima Salahshor
1) Companion diagnostics are tests that are essential for the safe and effective use of a corresponding drug or therapeutic product. Complementary diagnostics provide additional information that may predict treatment response but are not required for determining treatment.
2) Companion diagnostic tests identify biomarkers that indicate whether a patient is likely or unlikely to respond to a targeted drug. For example, the KRAS companion diagnostic predicts response to cetuximab for colorectal cancer.
3) The global cancer diagnostic market, including companion diagnostics, is large and growing as healthcare shifts toward personalized medicine approaches.
This investor presentation summarizes Oncolytics Biotech's clinical development plan for REOLYSIN, a viral immunotherapy for cancer. It discusses three pathways: 1) chemotherapy combinations, which are the basis for the first registration pathway in pancreatic cancer. Survival data from several phase 2 studies is expected in 2017. 2) Immunotherapy combinations, including an ongoing study of REOLYSIN with pembrolizumab. 3) Targeted agent/IMiD combinations, such as a collaboration using REOLYSIN with pomalidomide in multiple myeloma. The presentation outlines the mechanism of action of REOLYSIN and how combinations can enhance innate and adaptive immune responses against cancer.
SVMPharma Real World Evidence – Why NHS must embrace Real World DataSVMPharma Limited
SVMPharma Real World Evidence (RWE) – In this paper, we look at how to navigate the difficult balance between financial sustainability
and optimal performance the NHS needs to be more proactive in the collection and
analysis of Real World Data (RWD) and exploit the multiple opportunities for
commissioning RWD analysis at a local and national level . For more resources on RWE visit us at www.svmpharma.com
Your fast-pass to the news, insights, and storylines you need to know.
Watch the full webinar here http://ow.ly/4mOGmk
Hosted by Master of Ceremonies Ian Lloyd, senior director of Pharmaprojects and data integration, this webinar spotlights the blockbuster trends and rising stars of global R&D 2016 as seen in this year’s Annual Review.
During this presentation, Ian Lloyd & Scrip Managing Editor, Alex Shimmings cover:
>> Year-on-year growth
>> Clinical phases trends
>> Top companies and the shape of the industry
>> Mergers and acquisitions
>> Trending therapies, diseases, drug types and delivery routes
>> Mechanisms and drug targets
This webinar is the essential pharma R&D trend and forecast overview you need to be positioned for success in 2016.
Watch the full webinar here http://ow.ly/4mOGmk
Analyzing ASCO 2016: Developments, takeaways, and implications from the confe...Pharma Intelligence
In conjunction with a Key Opinion Leader, Dr. Peter Lee MD Chair, Department of Immuno-Oncology at City of Hope Comprehensive Cancer Center, CA, several Informa analysts discuss the major developments of the conference and key take-aways via a Webinar.
Watch our recording of Biomedtracker's Robert Jeng, Ph,D., Citeline's Allison Bruce, Scrip's Mary Jo Laffler, and Datamonitor Healthcare's Zachary McLellan as they download and debrief following the always-exciting ASCO weekend.
View and listen to the full webinar here https://www.youtube.com/watch?v=7yMsCb3R5X8
Over 350 million people worldwide are suffering from rare diseases. Which is why it is necessary to understand the rare disease landscape to date.
Drug development is challenging at the best of times, and made even harder within the realm of rare diseases. Overall, the largest number of drugs has targeted indications within the therapeutic areas of oncology and infectious disease (ID), with malaria being an area of high interest with both therapeutic and preventive interventions.
View this slideshare to get the most accurate and timely intelligence about rare diseases drug development.
In this detailed 20-page report, containing numerous comparative graphs, you will discover:
- The top 25 Rare Diseases by total drugs in development to date
- Current Rare Disease drug development landscape
- Top 15 originators of drugs in development for Rare Diseases (includes non-rare disease drug counts and % of portfolio dedicated to Rare Diseases)
- Therapeutic area distribution of rare diseases and drugs in development
- The top 5 Rare Diseases by drug count per therapeutic area (TA)
- Rare Infectious Diseases with 10 or more drugs in development
- The top 15 originators developing drugs for Rare Infectious Diseases
- Rare cancers with 10 or more drugs in development
- The top 15 originators developing drugs for rare cancers
- Non-ID, non-cancer Rare Diseases with 20 or more drugs in development
- The top 15 originators developing drugs for non-ID, non-cancer Rare Diseases
Complementary Tests and Companion Diagnostics in OncologyDr. Sima Salahshor
1) Companion diagnostics are tests that are essential for the safe and effective use of a corresponding drug or therapeutic product. Complementary diagnostics provide additional information that may predict treatment response but are not required for determining treatment.
2) Companion diagnostic tests identify biomarkers that indicate whether a patient is likely or unlikely to respond to a targeted drug. For example, the KRAS companion diagnostic predicts response to cetuximab for colorectal cancer.
3) The global cancer diagnostic market, including companion diagnostics, is large and growing as healthcare shifts toward personalized medicine approaches.
This investor presentation summarizes Oncolytics Biotech's clinical development plan for REOLYSIN, a viral immunotherapy for cancer. It discusses three pathways: 1) chemotherapy combinations, which are the basis for the first registration pathway in pancreatic cancer. Survival data from several phase 2 studies is expected in 2017. 2) Immunotherapy combinations, including an ongoing study of REOLYSIN with pembrolizumab. 3) Targeted agent/IMiD combinations, such as a collaboration using REOLYSIN with pomalidomide in multiple myeloma. The presentation outlines the mechanism of action of REOLYSIN and how combinations can enhance innate and adaptive immune responses against cancer.
SVMPharma Real World Evidence – Why NHS must embrace Real World DataSVMPharma Limited
SVMPharma Real World Evidence (RWE) – In this paper, we look at how to navigate the difficult balance between financial sustainability
and optimal performance the NHS needs to be more proactive in the collection and
analysis of Real World Data (RWD) and exploit the multiple opportunities for
commissioning RWD analysis at a local and national level . For more resources on RWE visit us at www.svmpharma.com
Personalised Medicine in the EU— Evolving Landscape and New HTA ConsiderationsOffice of Health Economics
The document discusses precision medicine and health technology assessment (HTA) of complementary diagnostics in Europe. It notes that precision medicine is moving from single biomarker tests to complex multi-parameter disease management, but markets have struggled to adopt even simple biomarkers. A new paper published by Epemed identifies additional elements of value for complementary diagnostics beyond traditional HTA considerations like life years gained and cost savings. These include reducing uncertainty, value of hope, and option value of future treatments. The paper recommends changing evidentiary requirements for HTA to consider broader clinical utility and value-based pricing approaches that account for all elements of value.
U.S. dependency on foreign pharmaceutical production imposes vulnerability to failure
Authors: Veronika Valdova, D.V.M. and Ronald L Sheckler
Affiliation: Arete-Zoe, LLC
ABSTRACT
Pharmaceutical supply chains have become increasingly complex due to the shift of manufacturing and critical operations to Asia. U.S. pharmaceutical dependency on foreign sole-source production of essential materials imposes vulnerability affecting the entire industry and national health systems from interruption by exposure to natural events and man-made threats, both accidental and criminal as well as political. Sector vulnerabilities stem from complex regulatory landscape, difficulties for enforcement of quality standards at foreign facilities, single-source supply chain resulting from limited sourcing options, increasing shipping distance exposure to both natural events and complicated by maritime chokepoints. Periodic and chronic shortages of many essential products across therapeutic categories have been significant for more than a decade. The Covid-19 crisis aggravated some of these long-standing issues and made the systemic vulnerabilities publicly evident. The combination of limited capacity to exercise control over essential commodities, the long-term trend of outsourcing, with the politicization of business relationships causes the entire pharmaceutical industrial sector to be internationally dependent, creating numerous potentials for systemic failure.
Oncolytics Biotech presented their investor presentation which included the following key points:
1) Oncolytics is developing REOLYSIN, a novel immuno-oncology viral agent for systemic administration that exploits cancer cell lysis and anti-tumor immunity.
2) Additional randomized phase 2 clinical trials in 2017 are expected to generate overall survival data in breast cancer, ovarian cancer, non-small cell lung cancer, and colorectal cancer.
3) The clinical development plan focuses on combining REOLYSIN with chemotherapy for late-stage development and establishing it as a backbone agent combined with immunotherapy.
4) Over 900 patients have been treated with REOLYSIN intravenously with no drug
Avoidable Patient Harm and Resulting Liability Arete-Zoe, LLC
Avoidable Patient Harm and Resulting Liability
What would it take to improve our insight into the cost of avoidable patient harm?
Medications are the most frequent cause of adverse events in clinical settings.
Some of the most devastating drug-related injuries include Steven-Johnson Syndrome, drug-related liver injury or bone marrow failure. These events, however rare, are among those that are very expensive to treat and often leave long-lasting damage.
The substantial consequences of adverse drug events are hospital admissions and readmissions, prolonged hospital stay, additional therapeutic interventions and increased demand on staff. For the patient, in addition to all the misery and pain they suffer, adverse drug events mean time away from work, loss of income and additional medical expenses.
Leerink Equity Research provides a catalyst tracker previewing top upcoming catalysts over the next 3-6 months for various healthcare stocks. Key events include data readouts from clinical trials that could significantly move stock prices depending on the results. The report lists dozens of stocks and their associated drug or product, indication, type of event, timeline, and estimated stock price impact. Upcoming catalysts highlighted include data presentations, regulatory decisions, product launches, and business development deals.
Cellgen Diagnostics is an early stage venture that is developing a break through Companion Diagnostic platform that will enable Precision Medicine by determining whether a patients genetic profile is a match for the prescribed cancer therapeutic.
The development & approval of Novoeight, a case studyAllen Che
The FDA approved Novoeight, a recombinant Factor VIII treatment for hemophilia A, in October 2013 based on positive results from clinical trials. Novoeight was found to effectively control and prevent bleeding episodes in adults and children with hemophilia A. The approval process involved reviewing manufacturing, clinical data, and inspections to ensure safety and efficacy. This approval expands treatment options for hemophilia A patients and represents continued innovation in the development of safer recombinant clotting factor therapies.
Ομιλία - Παρουσίαση: “Βιοδείκτες: Η Κλινική τους Αξία και η Σχέση τους με τον ΕΟΠΥΥ”
Νικόλαος Τσούλος, MSc, MBA, Βιοχημικός, Διευθύνων Σύμβουλος GeneKor Medical SA
Integrating Recent Data When Selecting First-line Antiretroviral Therapy.2015...Hivlife Info
Joseph J. Eron Jr., MD
W. David Hardy, MD
Paul E. Sax, MD
How do leading experts select first-line antiretroviral therapy for their HIV-infected patients?
Review these downloadable slides for key clinical trial data and the latest DHHS recommendations for first-line antiretroviral therapy.
Personalized medicine involves the prescription of specific therapeutics best suited for an individual based on their genetic or proteomic profile. This talk discusses current approaches in drug discovery/development, the role of genetics in drug metabolism, and lawful/ethical issues surrounding the deployment of new health technology.
Aligning on Patient Outcomes - How Market Dynamics Can Facilitate RWD SolutionsPAREXEL International
This document discusses how real-world data can be used to better understand patient outcomes. It notes that legislation, technology advances, and a shift toward valuing outcomes over volume are accelerating the focus on using real-world data to determine what treatment approaches improve patient outcomes. The document outlines challenges to using real-world data like data quality issues and privacy concerns, and proposes strategies like using hybrid study designs that combine electronic medical record data with traditional clinical trial data collection to help overcome these challenges. Finally, it emphasizes that solutions in this area will need to be developed incrementally while protecting patient privacy and gaining regulatory acceptance.
Use of open, curated variant databases: ethics? Liability? - Bartha KnoppersHuman Variome Project
Translation of genomics into medicine and drug development requires comprehensive, high-quality, genomic variant databases. To support translation, there is a movement towards sharing clinical annotations of variants (e.g., benign, unknown, pathogenic) internationally via open access. Despite the growing popularity of variant databases, ethical issues and liability risks have received scant attention. Ethical priorities for variant databases include 1) competence – ensuring that data is responsibly managed, curated, and used; 2) confidentiality – ensuring appropriate safeguards for patient data; 3) communication – clearly describing the purpose, quality standards, and data handling practices to contributing patients and potential users; and 4) continuous oversight to adapt database governance in a rapidly evolving environment. How can database managers fulfill these obligations when these responsibilities are increasingly distributed along the clinical pipeline? Legal issues include medical liability based on potential harm to patients; liability based on third-party intellectual property or privacy rights in the data; and regulatory risks as variant data is integrated into genetic tests or devices. Can these risks can be managed through appropriate governance structures – including adequate consents, access processes, contributor agreements, and disclaimers – while still facilitating sharing and clinical use?
This document provides an overview of key drivers that contributed to the strong performance of the healthcare sector in 2015. It discusses several secular trends that are positive for continued healthcare outperformance, including durable demand driven by demographics, growing affluence, and a shift to chronic diseases. Innovation is also accelerating due to genomic advances and increasing use of information technology. Regulatory and public policy trends are seen as positive, with the FDA approving drugs faster and policies expanding health insurance coverage. Overall, the healthcare sector remains attractively positioned for long-term growth.
ICIC 2014 Patent Landscape Analysis as a Tool for Public Policies Adjustment:...Dr. Haxel Consult
The innovative multinational pharmaceutical industry is highly dependent on the release and promotion of new drugs. However, recent economic evidence demonstrates a continuing decrease in new drugs’ market approval. Moreover, the industry is challenged by the “patent cliff”, where many blockbuster drugs are losing patent protection and facing ferocious competition.
It seems that the shortage of new drugs points to an intensification of drug development based on molecules already known, leading to incremental patents. However, there is a suspicion that many incremental patents are actually trivial, because they add little or nothing to existing therapies, but still impose high drug costs. To analyze that hypothesis, the present study has drawn the profile of all patents filed in Brazil in the antiretroviral (ARV) field up to 2012. Using VantagePoint® and Questel Orbit® softwares, a patent matrix was constructed with quali-quantitative data. Next, the patent applications' claims were analysed in order to detect incremental patents and classified according to their incrementalities. Finally we looked for evidence of triviality. As a result, it was demonstrated that the ARV market is highly concentrated and patent applications basically belong to six countries. Evidence that many incrementalities are actually trivialities and act as entry barriers, was found. Patent landscape studies such as this one can be extrapolated to other areas or countries, and can be used as a tool for public policy’s analysis to really fuel technological advance.
ROSALIND is a computer simulation program that uses a patient's tumor gene profile to evaluate all available cancer therapy options and predict the most effective treatments. It can simulate over 10,000 drug combinations in under 2 hours, allowing for a comprehensive and fast analysis. ROSALIND's predictions aim to personalize cancer treatment for each patient and help guide them to therapies with the highest chance of remission or available clinical trials when standard options are unlikely to work. The company envisions ROSALIND being widely adopted to achieve higher remission rates and lower healthcare costs through more personalized cancer care.
2015 10-06 Building Bridges Biomarker symposium FIMM Helsinki, Alain van GoolAlain van Gool
A unique honour and opportunity to give a 1.5 hour lecture to young biomarker scientists to introduce biomarkers and their importance in translational medicine and personalized healthcare.
Art 923 rev-c-updating investor presentation on valeritas website_final_12.05.16valeritasir
V-Go is a single-use, fully disposable insulin delivery device that provides basal and bolus insulin. It addresses the needs of the 4.6 million Type 2 diabetes patients in the US who require insulin but are not achieving treatment goals. Extensive clinical data shows V-Go lowers A1C levels and total daily insulin dose. It has established reimbursement through pharmacy benefits, making it cost-neutral for payors and patients compared to insulin pens. Valeritas sees significant growth opportunities by expanding its sales force to reach more prescribers.
New drug approvals & upcoming fda approvals 2021DoriaFang
In the first half of 2021, the U.S. FDA approved a total of 29 innovative drugs, of which 27 were new molecular entities and new biologics approved by the Center for Drug Evaluation and Research (CDER) and the remaining two were Car-T therapies (Abecma and Breyanzi) approved by the Center for Biologics Evaluation and Research (CBER).
Regenerative Medicine Industry Outlook 2014Pete Shuster
The document summarizes the regenerative medicine field based on a report from the Alliance for Regenerative Medicine, including an overview of major industry players and subsectors, clinical trials and products in development, financial performance and investments in 2013, and insights from a panel discussion on key areas of focus. It analyzes trends in cell and gene therapies, areas attracting pharmaceutical investment, and challenges facing the commercialization of regenerative medicine technologies and therapies.
Personalised Medicine in the EU— Evolving Landscape and New HTA ConsiderationsOffice of Health Economics
The document discusses precision medicine and health technology assessment (HTA) of complementary diagnostics in Europe. It notes that precision medicine is moving from single biomarker tests to complex multi-parameter disease management, but markets have struggled to adopt even simple biomarkers. A new paper published by Epemed identifies additional elements of value for complementary diagnostics beyond traditional HTA considerations like life years gained and cost savings. These include reducing uncertainty, value of hope, and option value of future treatments. The paper recommends changing evidentiary requirements for HTA to consider broader clinical utility and value-based pricing approaches that account for all elements of value.
U.S. dependency on foreign pharmaceutical production imposes vulnerability to failure
Authors: Veronika Valdova, D.V.M. and Ronald L Sheckler
Affiliation: Arete-Zoe, LLC
ABSTRACT
Pharmaceutical supply chains have become increasingly complex due to the shift of manufacturing and critical operations to Asia. U.S. pharmaceutical dependency on foreign sole-source production of essential materials imposes vulnerability affecting the entire industry and national health systems from interruption by exposure to natural events and man-made threats, both accidental and criminal as well as political. Sector vulnerabilities stem from complex regulatory landscape, difficulties for enforcement of quality standards at foreign facilities, single-source supply chain resulting from limited sourcing options, increasing shipping distance exposure to both natural events and complicated by maritime chokepoints. Periodic and chronic shortages of many essential products across therapeutic categories have been significant for more than a decade. The Covid-19 crisis aggravated some of these long-standing issues and made the systemic vulnerabilities publicly evident. The combination of limited capacity to exercise control over essential commodities, the long-term trend of outsourcing, with the politicization of business relationships causes the entire pharmaceutical industrial sector to be internationally dependent, creating numerous potentials for systemic failure.
Oncolytics Biotech presented their investor presentation which included the following key points:
1) Oncolytics is developing REOLYSIN, a novel immuno-oncology viral agent for systemic administration that exploits cancer cell lysis and anti-tumor immunity.
2) Additional randomized phase 2 clinical trials in 2017 are expected to generate overall survival data in breast cancer, ovarian cancer, non-small cell lung cancer, and colorectal cancer.
3) The clinical development plan focuses on combining REOLYSIN with chemotherapy for late-stage development and establishing it as a backbone agent combined with immunotherapy.
4) Over 900 patients have been treated with REOLYSIN intravenously with no drug
Avoidable Patient Harm and Resulting Liability Arete-Zoe, LLC
Avoidable Patient Harm and Resulting Liability
What would it take to improve our insight into the cost of avoidable patient harm?
Medications are the most frequent cause of adverse events in clinical settings.
Some of the most devastating drug-related injuries include Steven-Johnson Syndrome, drug-related liver injury or bone marrow failure. These events, however rare, are among those that are very expensive to treat and often leave long-lasting damage.
The substantial consequences of adverse drug events are hospital admissions and readmissions, prolonged hospital stay, additional therapeutic interventions and increased demand on staff. For the patient, in addition to all the misery and pain they suffer, adverse drug events mean time away from work, loss of income and additional medical expenses.
Leerink Equity Research provides a catalyst tracker previewing top upcoming catalysts over the next 3-6 months for various healthcare stocks. Key events include data readouts from clinical trials that could significantly move stock prices depending on the results. The report lists dozens of stocks and their associated drug or product, indication, type of event, timeline, and estimated stock price impact. Upcoming catalysts highlighted include data presentations, regulatory decisions, product launches, and business development deals.
Cellgen Diagnostics is an early stage venture that is developing a break through Companion Diagnostic platform that will enable Precision Medicine by determining whether a patients genetic profile is a match for the prescribed cancer therapeutic.
The development & approval of Novoeight, a case studyAllen Che
The FDA approved Novoeight, a recombinant Factor VIII treatment for hemophilia A, in October 2013 based on positive results from clinical trials. Novoeight was found to effectively control and prevent bleeding episodes in adults and children with hemophilia A. The approval process involved reviewing manufacturing, clinical data, and inspections to ensure safety and efficacy. This approval expands treatment options for hemophilia A patients and represents continued innovation in the development of safer recombinant clotting factor therapies.
Ομιλία - Παρουσίαση: “Βιοδείκτες: Η Κλινική τους Αξία και η Σχέση τους με τον ΕΟΠΥΥ”
Νικόλαος Τσούλος, MSc, MBA, Βιοχημικός, Διευθύνων Σύμβουλος GeneKor Medical SA
Integrating Recent Data When Selecting First-line Antiretroviral Therapy.2015...Hivlife Info
Joseph J. Eron Jr., MD
W. David Hardy, MD
Paul E. Sax, MD
How do leading experts select first-line antiretroviral therapy for their HIV-infected patients?
Review these downloadable slides for key clinical trial data and the latest DHHS recommendations for first-line antiretroviral therapy.
Personalized medicine involves the prescription of specific therapeutics best suited for an individual based on their genetic or proteomic profile. This talk discusses current approaches in drug discovery/development, the role of genetics in drug metabolism, and lawful/ethical issues surrounding the deployment of new health technology.
Aligning on Patient Outcomes - How Market Dynamics Can Facilitate RWD SolutionsPAREXEL International
This document discusses how real-world data can be used to better understand patient outcomes. It notes that legislation, technology advances, and a shift toward valuing outcomes over volume are accelerating the focus on using real-world data to determine what treatment approaches improve patient outcomes. The document outlines challenges to using real-world data like data quality issues and privacy concerns, and proposes strategies like using hybrid study designs that combine electronic medical record data with traditional clinical trial data collection to help overcome these challenges. Finally, it emphasizes that solutions in this area will need to be developed incrementally while protecting patient privacy and gaining regulatory acceptance.
Use of open, curated variant databases: ethics? Liability? - Bartha KnoppersHuman Variome Project
Translation of genomics into medicine and drug development requires comprehensive, high-quality, genomic variant databases. To support translation, there is a movement towards sharing clinical annotations of variants (e.g., benign, unknown, pathogenic) internationally via open access. Despite the growing popularity of variant databases, ethical issues and liability risks have received scant attention. Ethical priorities for variant databases include 1) competence – ensuring that data is responsibly managed, curated, and used; 2) confidentiality – ensuring appropriate safeguards for patient data; 3) communication – clearly describing the purpose, quality standards, and data handling practices to contributing patients and potential users; and 4) continuous oversight to adapt database governance in a rapidly evolving environment. How can database managers fulfill these obligations when these responsibilities are increasingly distributed along the clinical pipeline? Legal issues include medical liability based on potential harm to patients; liability based on third-party intellectual property or privacy rights in the data; and regulatory risks as variant data is integrated into genetic tests or devices. Can these risks can be managed through appropriate governance structures – including adequate consents, access processes, contributor agreements, and disclaimers – while still facilitating sharing and clinical use?
This document provides an overview of key drivers that contributed to the strong performance of the healthcare sector in 2015. It discusses several secular trends that are positive for continued healthcare outperformance, including durable demand driven by demographics, growing affluence, and a shift to chronic diseases. Innovation is also accelerating due to genomic advances and increasing use of information technology. Regulatory and public policy trends are seen as positive, with the FDA approving drugs faster and policies expanding health insurance coverage. Overall, the healthcare sector remains attractively positioned for long-term growth.
ICIC 2014 Patent Landscape Analysis as a Tool for Public Policies Adjustment:...Dr. Haxel Consult
The innovative multinational pharmaceutical industry is highly dependent on the release and promotion of new drugs. However, recent economic evidence demonstrates a continuing decrease in new drugs’ market approval. Moreover, the industry is challenged by the “patent cliff”, where many blockbuster drugs are losing patent protection and facing ferocious competition.
It seems that the shortage of new drugs points to an intensification of drug development based on molecules already known, leading to incremental patents. However, there is a suspicion that many incremental patents are actually trivial, because they add little or nothing to existing therapies, but still impose high drug costs. To analyze that hypothesis, the present study has drawn the profile of all patents filed in Brazil in the antiretroviral (ARV) field up to 2012. Using VantagePoint® and Questel Orbit® softwares, a patent matrix was constructed with quali-quantitative data. Next, the patent applications' claims were analysed in order to detect incremental patents and classified according to their incrementalities. Finally we looked for evidence of triviality. As a result, it was demonstrated that the ARV market is highly concentrated and patent applications basically belong to six countries. Evidence that many incrementalities are actually trivialities and act as entry barriers, was found. Patent landscape studies such as this one can be extrapolated to other areas or countries, and can be used as a tool for public policy’s analysis to really fuel technological advance.
ROSALIND is a computer simulation program that uses a patient's tumor gene profile to evaluate all available cancer therapy options and predict the most effective treatments. It can simulate over 10,000 drug combinations in under 2 hours, allowing for a comprehensive and fast analysis. ROSALIND's predictions aim to personalize cancer treatment for each patient and help guide them to therapies with the highest chance of remission or available clinical trials when standard options are unlikely to work. The company envisions ROSALIND being widely adopted to achieve higher remission rates and lower healthcare costs through more personalized cancer care.
2015 10-06 Building Bridges Biomarker symposium FIMM Helsinki, Alain van GoolAlain van Gool
A unique honour and opportunity to give a 1.5 hour lecture to young biomarker scientists to introduce biomarkers and their importance in translational medicine and personalized healthcare.
Art 923 rev-c-updating investor presentation on valeritas website_final_12.05.16valeritasir
V-Go is a single-use, fully disposable insulin delivery device that provides basal and bolus insulin. It addresses the needs of the 4.6 million Type 2 diabetes patients in the US who require insulin but are not achieving treatment goals. Extensive clinical data shows V-Go lowers A1C levels and total daily insulin dose. It has established reimbursement through pharmacy benefits, making it cost-neutral for payors and patients compared to insulin pens. Valeritas sees significant growth opportunities by expanding its sales force to reach more prescribers.
New drug approvals & upcoming fda approvals 2021DoriaFang
In the first half of 2021, the U.S. FDA approved a total of 29 innovative drugs, of which 27 were new molecular entities and new biologics approved by the Center for Drug Evaluation and Research (CDER) and the remaining two were Car-T therapies (Abecma and Breyanzi) approved by the Center for Biologics Evaluation and Research (CBER).
Regenerative Medicine Industry Outlook 2014Pete Shuster
The document summarizes the regenerative medicine field based on a report from the Alliance for Regenerative Medicine, including an overview of major industry players and subsectors, clinical trials and products in development, financial performance and investments in 2013, and insights from a panel discussion on key areas of focus. It analyzes trends in cell and gene therapies, areas attracting pharmaceutical investment, and challenges facing the commercialization of regenerative medicine technologies and therapies.
- IDXG provides molecular diagnostic tests for cancer risk assessment and prognosis.
- Recent accomplishments include new product launches, reimbursement from Aetna for ThyraMir, and achieving approval in New York State.
- The presentation provides financial information, with revenue growing but losses continuing from investments in sales, R&D and administrative expenses.
The document provides an overview of the global liquid biopsy market forecast from 2020 to 2025. It discusses key aspects of the market such as application, end user, clinical application, product/service, circulating biomarker, technology, and region. It also profiles major companies in the market and their recent developments. The global liquid biopsy market is expected to grow significantly due to the rising adoption of non-invasive cancer screening and monitoring techniques. However, lack of standardization and low reimbursement rates may hinder the market growth.
1706 ir deck full w_appendix v1_cmd_v6_uten appendixtargovax2017
The document summarizes a capital markets update presentation by Targovax. It discusses Targovax's two immunotherapy platforms - ONCOS-102, an oncolytic virus, and TG01, a peptide cancer vaccine. For ONCOS-102, the virus is injected into tumors where it stimulates an immune response by releasing cancer antigens. TG01 mimics antigens to stimulate "killer" T-cells. Early clinical trial results for ONCOS-102 showed increased tumor-infiltrating T-cells and systemic immune responses in cancer patients. Targovax is pursuing multiple clinical trials to combine its immunotherapies with other treatments.
1706 ir deck full w_appendix v1_cmd_v12_netttargovax2017
The document discusses Targovax's TG01 peptide vaccine platform. TG01 primes the immune system to recognize and destroy cancer cells with RAS mutations through a cocktail of 7 peptides covering common RAS mutations. Earlier trials in pancreatic cancer showed encouraging median and 1-year survival rates compared to historical controls when TG01 was administered with GM-CSF adjuvant. Long-term survival data also correlated with immune responses detected following vaccination.
The document discusses the current state and expected growth trends of the in vitro diagnostics (IVD) market. It notes that the global IVD market was estimated at $54.2 billion in 2013 and is expected to grow 4% annually to $64.3 billion by 2018. Technological advances in areas like genomics, bioinformatics, and miniaturization have transformed diagnostic laboratory technology in recent years. Personalized medicine, infectious disease testing, and other applications are driving growth in the IVD market. However, economic instability, rising healthcare costs, and reimbursement changes pose challenges for the industry.
The document discusses producing DECAPEPTYL (triptorelin), a prostate cancer drug, locally in Iran. It provides background on prostate cancer epidemiology and treatment in Iran. It then analyzes the Iranian pharmaceutical market, DECAPEPTYL's competitors, pricing strategies, and a potential transition pathway for local production. Forecasts and action plans are proposed to improve Ferring Pharmaceuticals' position in the Iranian market by taking advantage of new rules allowing local manufacturing.
The value of early asset development and commercializationCello Health
Worldwide pharmaceutical R&D spend is increasing each year, and the competition for a share of that investment is becoming fiercer. Companies need to demonstrate the potential value of their asset in commercial as well as scientific and clinical terms.
The slides in this deck define and identify value from a financial, clinical and commercial perspective while also exploring how to derive value for patients.
Just to remind you that registrations for our 18th Pharmacovigilance 2019 event, which is taking place at The Pestana Chelsea Bridge Hotel in London, UK on 27-28th Feb are closing soon.For more details email to dinesh@virtueinsightsummits.com
MDxHealth provides molecular diagnostic tests to improve diagnosis and treatment decisions for urological cancers like prostate and bladder cancer. Their lead product is ConfirmMDx, which helps determine if a repeat biopsy is needed after an initial negative biopsy result. They are also launching SelectMDx, a urine-based test to improve patient selection for initial biopsies. Looking forward, they plan to expand their product portfolio and commercial footprint in the US and EU to address unmet needs in urological cancer testing and help reduce unnecessary invasive procedures.
This document provides an overview of Bayer HealthCare as of March 2011. It discusses the company's structure, key financial data, business areas, research and development activities, and goals for strengthening its position in pharmaceuticals, consumer health, and emerging markets. Bayer HealthCare aims to be a leading diversified healthcare company through innovation, building strong brands, and expanding in high-growth areas.
This document provides information about an upcoming pharmacovigilance conference in 2016 including the key speakers, exhibitors, sponsors, agenda, and registration details. The conference will cover topics such as current regulatory trends in inspections, signal detection, social media in pharmacovigilance, data mining technology, and contemporary regulatory scenarios. It will gather professionals from pharmacovigilance, drug safety, epidemiology, and regulatory affairs from the pharmaceutical, biotechnology, and CRO industries.
The document discusses liquid biopsies and next generation cancer molecular diagnostics. It summarizes that OncoCyte Corporation is focused on developing diagnostic tests for early cancer detection using liquid biopsies, with an initial focus on tests for lung cancer. Key points include that lung cancer diagnostics represents a large market opportunity and that OncoCyte's preliminary lung cancer diagnostic test shows strong performance in clinical trials with high sensitivity and specificity. The test has the potential to reduce risky follow-up procedures for patients and provide significant healthcare cost savings.
Viatar CTC Solutions Inc. is a medical technology company focused on the treatment of patients with metastatic cancer. The Company's lead product, the Viatar™ Therapeutic Oncopheresis System, removes circulating tumor cells (CTCs) from whole blood using label-free cross-flow filtration. It is designed to be used as a periodic therapy to improve overall survival for a wide range of solid tumor types such as lung, breast, colon, prostate, and gastric cancers. This proprietary technology also powers the Company's liquid biopsy products, which are collection systems for use by genetic testing companies, researchers, and medical oncologists that provide a greater quantity and purity of circulating tumor cells for their molecular analysis and personalized medicine objectives. The Company’s liquid biopsy products are currently generating revenue, and sales are expected to increase in the coming quarters.
Viatar is a medtech company focused on developing products to treat cancer patients. Its lead product, the Viatar Therapeutic Oncopheresis System, removes circulating tumor cells from blood to improve cancer outcomes. Animal studies show removing CTCs can slow cancer progression and increase survival. The system may address a $1.5 billion market. Viatar is also developing liquid biopsy products to collect CTCs for cancer screening and research. The company expects to begin commercializing products in Europe in late 2016 and the US after additional clinical trials.
This presentation provides an overview of Interpace Diagnostics Group (IDXG), a commercial company that provides molecular diagnostic tests and pathology services. Key points:
- IDXG has proprietary molecular diagnostic tests for pancreatic cysts (PancraGEN), thyroid nodules (ThyGenX/ThyraMIR), and Barrett's esophagus (BarreGEN).
- Clinical studies show PancraGEN more accurately determines cancer risk of pancreatic cysts compared to current guidelines. ThyGenX/ThyraMIR combination testing can accurately rule in or rule out thyroid cancer risk.
- The tests have significant market opportunities and address unmet clinical needs to avoid unnecessary surgeries and
The document provides an overview and highlights from Targovax's first quarter 2018 presentation. Some key points:
- Targovax has two immuno-oncology programs in clinical development, ONCOS-102 and ONCOS TG.
- In the mesothelioma trial, the safety lead-in cohort of 6 patients was completed without safety concerns and showed signs of immune activation and early clinical responses in 3 patients.
- Targovax has a sound financial position with cash to fund its planned clinical program into 2019 and is listed on the Oslo Stock Exchange.
This report provides comprehensive information on the therapeutic development for Brain Cancer, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Brain Cancer and special features on late-stage and discontinued projects.
http://www.researchmoz.us/brain-cancer-pipeline-review-h1-2015-report.html
Similar to Global Transactions in Pharma/Biotech (20)
The 2017 Scrip Awards are accepting entries.
For the last 12 years, the Scrip Awards has applauded the essential role the pharmaceutical, biotech and other allied industries play in improving healthcare, with trophies spanning the entire range of industry activities, from new drug launches and clinical trials, to innovative deals, outsourcing and fundraising.
This year we have an exciting new category to reward the successes of business development teams, whether they are from a pharma or biotech company or a cross-company team responsible for a specific deal or collaborative project.
The Scrip Awards has carved out a unique place in the industry calendar, with attendees coming far and wide to the prestigious ceremony, which this year will take place in the London Hilton on Park Lane in Mayfair on 29 November.
Our panel of 16 highly respected and independent experts from across the sector is waiting to judge the entries from the 16 categories in contention this year. Now is the time to prepare your entry and make sure you take your opportunity to shine.
Find out more information here http://www.scripawards.com/enter/
To purchase the full report follow this link https://goo.gl/kKrtGt
Using in-house sales forecasts, this analysis explores and visualizes market dynamics in the Big Pharma peer set out to 2025. PharmaVitae casts its eye out to 2025 as crystallizing trends in healthcare management will influence Big Pharma to further position itself towards providing value. Big Pharma will add $39bn in revenues out to 2025, generating $464bn in prescription pharmaceuticals at a low single-digit compound annual growth rate of 0.9%. A healthy launch portfolio will bolster growth as Big Pharma reaps the reward of breakthrough products as the result of recent industry innovation. However, the low single-digit CAGR is representative of the overall drag that Big Pharma is facing. Three themes will shape the outlook: evolving business models, market access, and productivity.
Key questions answered
Revenue analysis
Which will be the best performing companies out to 2025?
Which companies will propel revenue growth over the forecast period?
How will Big Pharma perform across the US, 5EU, Japan and RoW regions?
Which companies will have leading market share gains and market share losses?
Therapy area analysis
How are late-stage pipelines positioned and what are the most-coveted launch products?
How many new blockbuster positions will Big Pharma carve out to 2025?
Which therapy areas will experience the largest growth and decline?
Where are companies building leadership positions in specific therapy areas?
What are the detailed competitive dynamics at play in the oncology, metabolic and, infectious diseases markets?
Strategy analysis
Will there be drastic shifts in the proportion of prescription drug revenue that is attributed to R&D?
How is Big Pharma using M&A to propel strategic goals?
What is the current status of biosimilar filings and how will they affect the performance of Big Pharma?
What strategies have been key for the commercial success of products launched in the past few years?
Highlights
Big Pharma prescription drug sales are forecast to grow to $464bn by 2025 at a compound annual growth rate of 0.9%
Number one company in 2025: Pfizer sustains top ranking in prescription drug sales out to 2025
Most valuable product: Humira will continue to be the highest selling product in 2025 with global sales forecast at $11bn
Most lucrative therapy area: Oncology will supplant metabolic in 2023 to become the most valuable therapy for Big Pharma
Most valuable class: PD-1/PD-L1 inhibitors will continue to build momentum out to 2025
Pipeline launch analysis: Big Pharma’s launch portfolio is set to add $134bn in revenues out to 2025
Most valuable company pipeline: Gilead will add pipeline revenues of $19bn out to 2025.
To purchase the full report follow this link https://goo.gl/kKrtGt
Will reimbursement prove to be the biggest barrier as three gene therapies gain regulatory approval?
Datamonitor Healthcare has carried out a comprehensive analysis of gene therapy products in commercial development worldwide based on information derived from Pharmaprojects. The results have been analyzed to reveal trends in gene therapy technologies and approaches to the treatment of different diseases.
The number of gene therapy products in preclinical to Phase III and beyond stages of development doubled between 2012 and 2015. Additionally, three gene therapy products – Glybera (uniQure), Imlygic (Amgen), and Strimvelis (GlaxoSmithKline) – have now received regulatory approval in Europe. While these approvals give some validation to gene therapy as a therapeutic strategy, doubts remain around their return on investment. The high upfront costs and residual uncertainty around the long-term benefits of gene therapy products are proving to be hurdles to wider access and reimbursement, but seem to have had a minimal impact on companies’ appetite to dive into this arena, with cancer and monogenic diseases proving to be the most popular indications for the development of gene therapy products.
For more information on this report visit https://pharmastore.informa.com/product/trends-gene-therapy/
Brexit: Issues And Opportunities As UK Life Sciences Define A New Relationshi...Pharma Intelligence
View the full webinar here http://bit.ly/Webinar_Brexit_Download
Sector specific concerns in the wake of the Brexit vote include potential changes to drug approval regulations, movement of researchers and executives into and out of the UK, the impact on investment and trade, and more.
Listen to:
Steve Bates, Chief Executive Officer, BIA
Virginia Acha, Executive Director, ABPI
Jo Pisani, Partner, PwC
Lindsey Barras, Director in Global Immigration, PwC
Harren Jhoti, President and CEO, Astex Pharmaceuticals
Ian Schofield, Principal Analyst, Scrip
Sukaina Virji, News Editor, Scrip (Chair)
They share insight on the following key areas:
Brexit: what do we actually know?
- Key concerns around regulation, people, trade and innovation
- Key elements of the government’s Brexit strategy
- What opportunities Brexit throws out for UK life sciences
View the full webinar here http://bit.ly/Webinar_Brexit_Download
The document summarizes coverage from Meddevicetracker on the recent EuroPCR event, an annual cardiovascular conference. It provides instructions on how to search Meddevicetracker's database to find information on events that occurred at EuroPCR 2016, including an example of results found for a trial on the Lotus heart valve. The database also allows viewing analyses of medical devices and technologies presented, such as a bioresorbable vascular scaffold called Fantom. Users can filter the competitive landscape by product type, with an example given focusing on drug-eluting stents.
Biologics in Asthma: Generics, reimbursement, and market potential Pharma Intelligence
While asthma has traditionally been considered a well-established market, there are still a number of key unmet needs that could drive further development, particularly among biologics.
In this complimentary webinar, our Datamonitor Healthcare analyst will discuss current and pending biologics being used to treat chronic asthma, including pricing and reimbursement issues, performance projections, targeted patient groups, and the impact of generics on the market.
View and listen to full webinar for free here https://www.youtube.com/watch?v=bNlUE-VH6Tc
In this report, we cover catalysts from 21 drugs, devices and diagnostics expected to occur in Q2 2016. We have also included a list of large Impact catalysts in the drug and device/diagnostic areas through Q2 2016 from our sister product, CatalystTracker. In addition, each drug’s likelihood of Phase/PDUFA review success and overall Likelihood of Approval (LOA) given their particular phase, drug class, and disease group are provided.
Our Early 2016 Outlook Report highlighted several high- impact catalysts. The results of these catalysts can be found on Page 5 of this report. Biomedtracker Likelihood of Approval (LOA) opinions successfully predicted 78% of catalyst outcomes that occurred in Early 2016.
We have provided a sample of this 52 page report - to download
your complimentary copy of Biomedtrackers & Meddevicetrackers Q2 2016 Outlook report, please use the following link http://ow.ly/BG9g3004er4
NURSING MANAGEMENT OF PATIENT WITH EMPHYSEMA .PPTblessyjannu21
Prepared by Prof. BLESSY THOMAS, VICE PRINCIPAL, FNCON, SPN.
Emphysema is a disease condition of respiratory system.
Emphysema is an abnormal permanent enlargement of the air spaces distal to terminal bronchioles, accompanied by destruction of their walls and without obvious fibrosis.
Emphysema of lung is defined as hyper inflation of the lung ais spaces due to obstruction of non respiratory bronchioles as due to loss of elasticity of alveoli.
It is a type of chronic obstructive
pulmonary disease.
It is a progressive disease of lungs.
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - ...rightmanforbloodline
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - 34.
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - 34.
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - 34.
This particular slides consist of- what is Pneumothorax,what are it's causes and it's effect on body, risk factors, symptoms,complications, diagnosis and role of physiotherapy in it.
This slide is very helpful for physiotherapy students and also for other medical and healthcare students.
Here is a summary of Pneumothorax:
Pneumothorax, also known as a collapsed lung, is a condition that occurs when air leaks into the space between the lung and chest wall. This air buildup puts pressure on the lung, preventing it from expanding fully when you breathe. A pneumothorax can cause a complete or partial collapse of the lung.
nursing management of patient with Empyema pptblessyjannu21
prepared by Prof. BLESSY THOMAS, SPN
Empyema is a disease of respiratory system It is defines as the accumulation of thick, purulent fluid within the pleural space, often with fibrin development.
Empyema is also called pyothorax or purulent pleuritis.
It’s a condition in which pus gathers in the area between the lungs and the inner surface of the chest wall. This area is known as the pleural space.
Pus is a fluid that’s filled with immune cells, dead cells, and bacteria.
Pus in the pleural space can’t be coughed out. Instead, it needs to be drained by a needle or surgery.
Empyema usually develops after pneumonia, which is an infection of the lung tissue. it is mainly caused due in infectious micro-organisms. It can be treated with medications and other measures.
As Mumbai's premier kidney transplant and donation center, L H Hiranandani Hospital Powai is not just a medical facility; it's a beacon of hope where cutting-edge science meets compassionate care, transforming lives and redefining the standards of kidney health in India.
Solution manual for managerial accounting 18th edition by ray garrison eric n...rightmanforbloodline
Solution manual for managerial accounting 18th edition by ray garrison eric noreen and peter brewer_compressed
Solution manual for managerial accounting 18th edition by ray garrison eric noreen and peter brewer_compressed
English Drug and Alcohol Commissioners June 2024.pptxMatSouthwell1
Presentation made by Mat Southwell to the Harm Reduction Working Group of the English Drug and Alcohol Commissioners. Discuss stimulants, OAMT, NSP coverage and community-led approach to DCRs. Focussing on active drug user perspectives and interests
The Ultimate Guide in Setting Up Market Research System in Health-TechGokul Rangarajan
How to effectively start market research in the health tech industry by defining objectives, crafting problem statements, selecting methods, identifying data collection sources, and setting clear timelines. This guide covers all the preliminary steps needed to lay a strong foundation for your research.
"Market Research it too text-booky, I am in the market for a decade, I am living research book" this is what the founder I met on the event claimed, few of my colleagues rolled their eyes. Its true that one cannot over look the real life experience, but one cannot out beat structured gold mine of market research.
Many 0 to 1 startup founders often overlook market research, but this critical step can make or break a venture, especially in health tech.
But Why do they skip it?
Limited resources—time, money, and manpower—are common culprits.
"In fact, a survey by CB Insights found that 42% of startups fail due to no market need, which is like building a spaceship to Mars only to realise you forgot the fuel."
Sudharsan Srinivasan
Operational Partner Pitchworks VC Studio
Overconfidence in their product’s success leads founders to assume it will naturally find its market, especially in health tech where patient needs, entire system issues and regulatory requirements are as complex as trying to perform brain surgery with a butter knife. Additionally, the pressure to launch quickly and the belief in their own intuition further contribute to this oversight. Yet, thorough market research in health tech could be the key to transforming a startup's vision into a life-saving reality, instead of a medical mishap waiting to happen.
Example of Market Research working
Innovaccer, founded by Abhinav Shashank in 2014, focuses on improving healthcare delivery through data-driven insights and interoperability solutions. Before launching their platform, Innovaccer conducted extensive market research to understand the challenges faced by healthcare organizations and the potential for innovation in healthcare IT.
Identifying Pain Points: Innovaccer surveyed healthcare providers to understand their difficulties with data integration, care coordination, and patient engagement. They found widespread frustration with siloed systems and inefficient workflows.
Competitive Analysis: Analyzed competitors offering similar solutions in healthcare analytics and interoperability. Identified gaps in comprehensive data aggregation, real-time analytics, and actionable insights.
Regulatory Compliance: Ensured their platform complied with HIPAA and other healthcare data privacy regulations. This compliance was crucial to gaining trust from healthcare providers wary of data security issues.
Customer Validation: Conducted pilot programs with several healthcare organizations to validate the platform's effectiveness in improving care outcomes and operational efficiency. Gathered feedback to refine features and user interface.
VEDANTA AIR AMBULANCE SERVICES IN REWA AT A COST-EFFECTIVE PRICE.pdfVedanta A
Air Ambulance Services In Rewa works in close coordination with ground-based emergency services, including local Emergency Medical Services, fire departments, and law enforcement agencies.
More@: https://tinyurl.com/2shrryhx
More@: https://tinyurl.com/5n8h3wp8
Test bank clinical nursing skills a concept based approach 4e pearson educati...rightmanforbloodline
Test bank clinical nursing skills a concept based approach 4e pearson education
Test bank clinical nursing skills a concept based approach 4e pearson education
Test bank clinical nursing skills a concept based approach 4e pearson education
Emotional and Behavioural Problems in Children - Counselling and Family Thera...PsychoTech Services
A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
This particular slides consist of- what is hypotension,what are it's causes and it's effect on body, risk factors, symptoms,complications, diagnosis and role of physiotherapy in it.
This slide is very helpful for physiotherapy students and also for other medical and healthcare students.
Here is the summary of hypotension:
Hypotension, or low blood pressure, is when the pressure of blood circulating in the body is lower than normal or expected. It's only a problem if it negatively impacts the body and causes symptoms. Normal blood pressure is usually between 90/60 mmHg and 120/80 mmHg, but pressures below 90/60 are generally considered hypotensive.
1. Trials, Tech and Transformation
May 11, 2017
Patricia Giglio, Content Manager
Rachel Meighan-Mantha, Principal Analyst, Oncology
Steven Muntner, Vice President, Deals
Global Transactions in
Pharma/Biotech – trends in
partnering, M&A, clinical trials
and new drug combinations
21. Pharma intelligence | informa21
Pharma/Biotech Partnerships – Average Royalty Rate
0%
2%
4%
6%
8%
10%
12%
14%
16%
All Partnerships Oncology Partnerships I-O Partnerships
n=133 n=69 n=20n=46 n=26 n=5
n=83 n=83 n=12n=30 n=10 n=2
RoyaltyRate
2012- 2016
PreClinical Phase I Phase II Phase III
Source: Medtrack
22. Pharma intelligence | informa22
Pharma/Biotech Partnerships – Volume by Phase
0
50
100
150
200
250
300
PC I II III PA A M PM
NumberofDeals
2012 2013 2014 2015 2016
Source: Medtrack