Are there reasons for believing that the profitability of the industry might come under threat over the next decade what do you think managers in the industry should do to counter this threat
Managers in the pharmaceutical industry face both opportunities and threats due to a dynamic environment. Demand for pharmaceuticals has grown steadily for decades due to demographics and successful new drugs can be highly profitable. However, developing new drugs takes 10-15 years and costs $800 million on average, with many failing. Additionally, incumbent firms face challenges such as upcoming patent expirations, potential price controls, and reduced prices negotiated by large health providers.
> Why HEOR?
> Costs, Consequences and Perspectives
> Key Stakeholders in HEOR
> What is Health Economics and Pharmaco-economic Research?
> Economic Evaluations
> Incremental Cost Effectiveness Ratio (ICER)
> Concept of HRQoL
> Comparative Effectiveness Research (CER)
> Pragmatic Clinical Trials
> Observational Studies
> Systematic Reviews and Meta-Analysis
> Application of CER
> Health Technology Assessment (HTA)
> Real World Evidence (RWE)
> Patient Reported Outcomes (PROs)
> Patient Focused Drug Development (PFDD)
> Application of Health Economic Evaluations
> Challenges and Barriers
The philippines market research presentationNadia Dias
This Market Study was carried out during my internship training period at Wallace Pharmaceuticals, India, Pvt. Ltd.
it is a presentation proposal to the company in view of making future investment in the Philippine Pharmaceutical Market.
The Philippines pharmaceutical market is a complex institution owing to its expensive medical care, monopolistic competition, and lack of government controlled drug pricing, all within a country that has high levels of poverty.
The research study delves further into the pharmaceutical market, methods of investment and the advantages of investment in the said market.
N.B: This presentation is based solely on secondary internet research. Though 100% accurate and cited, some information (figures) are dated due to lack of current and up to date information availability on the internet.
The presentation is part of a market research study.
There are many areas to focus on when taking steps towards improving clinical trial operations. This presentation focuses on 4 areas: Patient Enrollment, Study Start-up, Monitoring, and Project Management.
Type ii diabetes case study for Drug LaunchKoushik Sircar
An attempt to provide a brief on Market Entry for New Add-On Drug ( Secondary Care) within Type-II Diabetes Market- focused on Add-on Drugs Data Analysis, Visualizations, Growth Share Matrix and Frameworks for Market Entry
> Why HEOR?
> Costs, Consequences and Perspectives
> Key Stakeholders in HEOR
> What is Health Economics and Pharmaco-economic Research?
> Economic Evaluations
> Incremental Cost Effectiveness Ratio (ICER)
> Concept of HRQoL
> Comparative Effectiveness Research (CER)
> Pragmatic Clinical Trials
> Observational Studies
> Systematic Reviews and Meta-Analysis
> Application of CER
> Health Technology Assessment (HTA)
> Real World Evidence (RWE)
> Patient Reported Outcomes (PROs)
> Patient Focused Drug Development (PFDD)
> Application of Health Economic Evaluations
> Challenges and Barriers
The philippines market research presentationNadia Dias
This Market Study was carried out during my internship training period at Wallace Pharmaceuticals, India, Pvt. Ltd.
it is a presentation proposal to the company in view of making future investment in the Philippine Pharmaceutical Market.
The Philippines pharmaceutical market is a complex institution owing to its expensive medical care, monopolistic competition, and lack of government controlled drug pricing, all within a country that has high levels of poverty.
The research study delves further into the pharmaceutical market, methods of investment and the advantages of investment in the said market.
N.B: This presentation is based solely on secondary internet research. Though 100% accurate and cited, some information (figures) are dated due to lack of current and up to date information availability on the internet.
The presentation is part of a market research study.
There are many areas to focus on when taking steps towards improving clinical trial operations. This presentation focuses on 4 areas: Patient Enrollment, Study Start-up, Monitoring, and Project Management.
Type ii diabetes case study for Drug LaunchKoushik Sircar
An attempt to provide a brief on Market Entry for New Add-On Drug ( Secondary Care) within Type-II Diabetes Market- focused on Add-on Drugs Data Analysis, Visualizations, Growth Share Matrix and Frameworks for Market Entry
The Top Seven Healthcare Outcome Measures and Three Measurement EssentialsHealth Catalyst
Healthcare outcomes improvement can’t happen without effective outcomes measurement. Given the healthcare industry’s administrative and regulatory complexities, and the fact that health systems measure and report on hundreds of outcomes annually, this article adds much-needed clarity by reviewing the top seven outcome measures, including definitions, important nuances, and real-life examples. The top seven categories of outcome measures are:
Mortality
Readmissions
Safety of care
Effectiveness of care
Patient experience
Timeliness of care
Efficient use of medical imaging
CMS used these seven outcome measures to calculate overall hospital quality and arrive at its 2018 hospital star ratings. This article also reiterates the importance of outcomes measurement, clarifies how outcome measures are defined and prioritized, and recommends three essentials for successful outcomes measurement.
Each protocol typically specifies medications whose use is prohibited during the trial because of possible interactions
with the Investigational Medicinal Product. The identification of such medications in the actual trial data typically
involves a programming effort followed by manual review by a medical expert. This slide presents a method for the
identification while simultaneously documenting the whole selection process.
The war on drugs has taken a massive cost in human lives, making the US the world’s largest prison population, but drugs remain widely available and treatment resources are insufficient. The US government spent trillions of dollars incarcerating non-violent drug offenders that pose barriers to employment and stability.
Clinical study on human subjects according to all guidelines to form a ideal protocol and requirement to conduct clinical trial with very efficient way mainly considering to India and ICH associated countries
Everything you need to know about digital Therapeutics.
“Digital therapeutics have been on the market for about ten years, but there’s only been a few of them,” says Megan Coder, executive director of the Digital Therapeutics Alliance (DTA)
Digital Therapeutics is the new face of healthcare. It is a technology-driven subset of healthcare sector which is going to change the traditional way of medicine. diagnosis and treatment.
Adverse Event Reporting in Pharmacovigilance: Principles and ChallengesClinosolIndia
Adverse event reporting is a crucial component of pharmacovigilance, the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. Here are the principles and challenges associated with adverse event reporting in pharmacovigilance:
Principles:
Timeliness: Adverse events should be reported promptly to ensure timely assessment and appropriate action. Reporting delays can hinder the detection of safety signals and the implementation of necessary interventions.
Completeness: Comprehensive reporting of all relevant information regarding the adverse event is vital. This includes patient demographics, medical history, drug details (name, dose, route of administration), onset and duration of the event, outcomes, and any concomitant medications.
Causality Assessment: Adverse events should be evaluated for their potential causality with the suspected drug. This involves considering factors such as temporal relationship, dechallenge/rechallenge information, and the presence of alternative explanations or confounding factors.
Confidentiality and Privacy: Adverse event reporting must uphold patient confidentiality and privacy. Personal identifiable information should be protected, and data should be handled in accordance with applicable data protection regulations.
Collaboration and Communication: Effective communication and collaboration between healthcare professionals, regulatory authorities, pharmaceutical companies, and patients are essential. Sharing information and feedback helps in improving patient safety and optimizing the understanding of adverse events.
Market access the challenges for medical devices Amy Morgan
With increased incidences of reimbursement rejections by payers and a growing usage of pricing and reimbursement tools market access is becoming increasingly restricted…
> Definition of RWD
> RWD - Big Data Characteristics
> Sources of RWD
> Important Stakeholders
> Benefits of RWD
> Why Data Sharing is Important?
> Benefits of Data Sharing
> Who Benefits?
> Ultimate Goals
> Case Studies
> Challenges
> Data Privacy Scenario
> Data Security in India
> Regulatory Perspectives Around RWD
> How to Encourage Data Sharing?
Combat the confusion surrounding the changes associated with Heath Care Reform and make sure your marketing plans are suited to thrive in this new environment. Plus, take advantage of our 2015 Essential Marketing Checklist to help you stay ahead of your competitors with your acquisition efforts, while simultaneously maintaining member retention.
The Top Seven Healthcare Outcome Measures and Three Measurement EssentialsHealth Catalyst
Healthcare outcomes improvement can’t happen without effective outcomes measurement. Given the healthcare industry’s administrative and regulatory complexities, and the fact that health systems measure and report on hundreds of outcomes annually, this article adds much-needed clarity by reviewing the top seven outcome measures, including definitions, important nuances, and real-life examples. The top seven categories of outcome measures are:
Mortality
Readmissions
Safety of care
Effectiveness of care
Patient experience
Timeliness of care
Efficient use of medical imaging
CMS used these seven outcome measures to calculate overall hospital quality and arrive at its 2018 hospital star ratings. This article also reiterates the importance of outcomes measurement, clarifies how outcome measures are defined and prioritized, and recommends three essentials for successful outcomes measurement.
Each protocol typically specifies medications whose use is prohibited during the trial because of possible interactions
with the Investigational Medicinal Product. The identification of such medications in the actual trial data typically
involves a programming effort followed by manual review by a medical expert. This slide presents a method for the
identification while simultaneously documenting the whole selection process.
The war on drugs has taken a massive cost in human lives, making the US the world’s largest prison population, but drugs remain widely available and treatment resources are insufficient. The US government spent trillions of dollars incarcerating non-violent drug offenders that pose barriers to employment and stability.
Clinical study on human subjects according to all guidelines to form a ideal protocol and requirement to conduct clinical trial with very efficient way mainly considering to India and ICH associated countries
Everything you need to know about digital Therapeutics.
“Digital therapeutics have been on the market for about ten years, but there’s only been a few of them,” says Megan Coder, executive director of the Digital Therapeutics Alliance (DTA)
Digital Therapeutics is the new face of healthcare. It is a technology-driven subset of healthcare sector which is going to change the traditional way of medicine. diagnosis and treatment.
Adverse Event Reporting in Pharmacovigilance: Principles and ChallengesClinosolIndia
Adverse event reporting is a crucial component of pharmacovigilance, the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. Here are the principles and challenges associated with adverse event reporting in pharmacovigilance:
Principles:
Timeliness: Adverse events should be reported promptly to ensure timely assessment and appropriate action. Reporting delays can hinder the detection of safety signals and the implementation of necessary interventions.
Completeness: Comprehensive reporting of all relevant information regarding the adverse event is vital. This includes patient demographics, medical history, drug details (name, dose, route of administration), onset and duration of the event, outcomes, and any concomitant medications.
Causality Assessment: Adverse events should be evaluated for their potential causality with the suspected drug. This involves considering factors such as temporal relationship, dechallenge/rechallenge information, and the presence of alternative explanations or confounding factors.
Confidentiality and Privacy: Adverse event reporting must uphold patient confidentiality and privacy. Personal identifiable information should be protected, and data should be handled in accordance with applicable data protection regulations.
Collaboration and Communication: Effective communication and collaboration between healthcare professionals, regulatory authorities, pharmaceutical companies, and patients are essential. Sharing information and feedback helps in improving patient safety and optimizing the understanding of adverse events.
Market access the challenges for medical devices Amy Morgan
With increased incidences of reimbursement rejections by payers and a growing usage of pricing and reimbursement tools market access is becoming increasingly restricted…
> Definition of RWD
> RWD - Big Data Characteristics
> Sources of RWD
> Important Stakeholders
> Benefits of RWD
> Why Data Sharing is Important?
> Benefits of Data Sharing
> Who Benefits?
> Ultimate Goals
> Case Studies
> Challenges
> Data Privacy Scenario
> Data Security in India
> Regulatory Perspectives Around RWD
> How to Encourage Data Sharing?
Combat the confusion surrounding the changes associated with Heath Care Reform and make sure your marketing plans are suited to thrive in this new environment. Plus, take advantage of our 2015 Essential Marketing Checklist to help you stay ahead of your competitors with your acquisition efforts, while simultaneously maintaining member retention.
Similar to Are there reasons for believing that the profitability of the industry might come under threat over the next decade what do you think managers in the industry should do to counter this threat
Global pharmaceutical companies are modeled with a supply chain, which ensures that the right drug reaches the right people at the right time and in the right condition. The supply chain also ensures 100% product availability at optimum cost by carrying huge inventory, which maintains 100% fill rate. Manufacturers are trying to cut down development time to save costs. For example, a drug manufacturer who can trim development time by 19% can save up to USD 100 million. But if a drug is getting delayed to reach the market, the time delay costs the company around USD 1 million a day. So, pharmaceutical companies today are designing the supply chain to be as responsive as possible to reduce entry time to the market thereby increasing profit margins.
Writekraft Research and Publications LLP was initially formed, informally, in 2006 by a group of scholars to help fellow students. Gradually, with several dissertations, thesis and assignments receiving acclaim and a good grade, Writekraft was officially founded in 2011 . Since its establishment, Writekraft Research & Publications LLP is Guiding and Mentoring PhD Scholars.
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Vision
Writekraft endeavours to be the leading global research and publications company that will fulfil all research needs of our clients. We will achieve this vision through:
Analyzing every customer’s aims, objectives and purpose of research
Using advanced and latest tools and technique of research and analysis
Coordinating and including their own ideas and knowledge
Providing the desired inferences and results of the research
In the past decade, we have successfully assisted students from various universities in India and globally. We at Writekraft Research & Publications LLP head office in Kanpur, India are most trusted and professional Research, Writing, Guidance and Publication Service Provider for PhD. Our services meet all your PhD Admissions, Thesis Preparation and Research Paper Publication needs with highest regards for the quality you prefer.
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We have PhD experts from reputed institutions/ organizations like Indian Institute of Technology (IIT), Indian Institute of Management (IIM) and many more apex education institutions in India. Our works are tailored and drafted as per your requirements and are totally unique.
From past years our core advisory members, research team assisted research scholars from various universities from all corners of world.
Writekraft Research and Publications LLP was initially formed, informally, in 2006 by a group of scholars to help fellow students. Gradually, with several dissertations, thesis and assignments receiving acclaim and a good grade, Writekraft was officially founded in 2011 . Since its establishment, Writekraft Research & Publications LLP is Guiding and Mentoring PhD Scholars.
Our Mission
“To provide breakthrough research works to our clients through Perseverant efforts towards creativity and innovation”.
Vision
Writekraft endeavours to be the leading global research and publications company that will fulfil all research needs of our clients. We will achieve this vision through:
Analyzing every customer’s aims, objectives and purpose of research
Using advanced and latest tools and technique of research and analysis
Coordinating and including their own ideas and knowledge
Providing the desired inferences and results of the research
In the past decade, we have successfully assisted students from various universities in India and globally. We at Writekraft Research & Publications LLP head office in Kanpur, India are most trusted and professional Research, Writing, Guidance and Publication Service Provider for PhD. Our services meet all your PhD Admissions, Thesis Preparation and Research Paper Publication needs with highest regards for the quality you prefer.
Our Achievements
NATIONAL AWARD FOR BEST RESEARCH PROJECT (By Hon. President APJ Abdul Kalam)
GOLD MEDAL FOR RESEARCH ON DISABILITY (By Disabled’s Club of India)
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Are there reasons for believing that the profitability of the industry might come under threat over the next decade what do you think managers in the industry should do to counter this threat
1. Managers in pharmaceutical firms face a dynamic and challenging task
environment that creates both opportunities and threats. Demand for
pharmaceuticals is strong and has been growing steadily for decades
Managers in pharmaceutical firms face a dynamic and challenging task
environment that creates both opportunities and threats. Demand for
pharmaceuticals is strong and has been growing steadily for decades
Assignment Solutions, Case study Answer sheets
Project Report and Thesis contact
aravind.banakar@gmail.com
www.mbacasestudyanswers.com
ARAVIND – 09901366442 – 09902787224
General Management
CASE: 1 THE PHARMACEUTICAL INDUSTRY
Managers in pharmaceutical firms face a dynamic and challenging task environment
that creates both opportunities and threats. Demand for pharmaceuticals is strong
and has been growing steadily for decades. Between 1990 and 2005 there was a 12.5
percent annual increase in spending on prescription drugs in United States. The
strong growth was driven by demographics. As people grow older they tend to
consume more prescription medicines, and the population in most advance nations
has been growing older as the post – World War II baby boom generation ages.
Moreover, successful new prescription drugs can be extraordinarily profitable.
Consider Lipitor, the cholesterol-lowering drug sold by Pfizer. Introduced in 1997, by
2005 this drug generated a staggering $12 billion in annual sales for Pfizer. The costs
of manufacturing, packaging, and distributing Lipitor amounted to only about 10
percent of revenues, or around $1.2 billion. Pfizer spent close to $400 million on
advertising and promoting Lipitor and perhaps as much again on maintaining a sales
force to sell the product. That still leaves Pfizer with a gross profit from Lipitor of
perhaps $10 billion.
2. Lipitor is highly profitable because the drug is protected from direct
competition by a 20-year patent. This temporary monopoly allows Pfizer to charge a
high price. Once the patent expires, other firms will be able to produce generic
versions of Lipitor, and the price will fall—typically by 80 percent within a year—but
that is some time away.
Competing firms can produce drugs that are similar (but not identical) to a
patent-protected drug. Drug firms patent a specific molecule, and competing firms
can patent similar, but not identical, molecules that have a similar pharmacological
effect. Thus Lipitor does have competitors in the market for cholesterol-lowering
drugs—such as Zocor, sold by Merck, and Crestor, sold by AstraZeneca. But these
competing drugs are also patent protected. Moreover, due to Federal Drug
Administration regulations and requirements for demonstrating that a drug is safe
and effective, the cost and risks associated with developing a new drug and bringing
it to market are very high. Out of 5,000 compounds tested in the laboratory by a drug
company, only five enter clinical trials, and only one of these will ultimately make it
to the market. On average, estimates suggest that it costs some $800 million and
takes anywhere from 10 to 15 years to bring a new drug to market. Once on the
market, on the market, only 3 out of 10 drugs ever recoup their R&D and marketing
costs and turn a profit. Thus the high profitability of the pharmaceutical industry
rests on a handful of blockbuster drugs. To produce a blockbuster, a drug company
must spend great amounts of money on research, most of which fails to produce a
product. Pfizer, for example, spent over $7.4 billion on R&D in 2005 alone,
equivalent to 14.6 percent of its total revenues.
In addition to R&D spending, the incumbent firms in the pharmaceutical
industry spend much money on advertising and sales promotion. Although the $400
million a year that Pfizer spends promoting Lipitor is small relative to the drug’s
revenues, it is a large amount for a new competitor to match, making market entry
difficult unless the competitor has a significantly better product.
There are also some big opportunities on the horizon for firms in the industry.
new scientific break-throughs in genomics portend that within the next decade
pharmaceutical firms might be able to bring new drugs to market that treat some of
3. the most intractable medical conditions, including Alzheimer’s, Parkinson’s disease,
cancer, heart disease, stroke, and HIV.
On the other hand, managers in the industry face serious challenges. Many
patent-protected medicines are scheduled to come off patent in the next decade, and
to maintain profitability, pharmaceutical firms must find new drugs to replace them.
In addition, as spending on health care rises, seniors are complaining about the high
costs of prescription medicines, and politicians are looking for ways to limit this. One
possibility is some form of price controls on prescription drugs. Pharmaceutical price
controls are already in effect in most developed nations, and although they have not
yet been introduced in the United States, that could happen. Another possibility is to
make it easy for U.S. residents to purchase pharmaceuticals from foreign nations
where prices are lower.
A further challenge is associated with the growth of large health care providers,
who have millions of subscribers and are starting to use their power to reduce the
drug prices their subscribers pay. In some cases they are refusing to provide
insurance coverage for high-priced pharmaceuticals when lower-priced generic
alternatives are available.
Questions
1. What are the barriers to entry into the pharmaceutical industry? To what
extent do you think these entries barriers protect established pharmaceutical
companies from new competitors?
2. The pharmaceutical industry has long been one of the most profitable in the
United States. Why do you think this is the case?
3. What forces in the general environment influence the nature of competition
in the task environment facing pharmaceutical firms?
4. 4. Are there reasons for believing that the profitability of the industry might come
under threat over the next decade? What do you think managers in the industry
should do to counter this threat?
Assignment Solutions, Case study Answer sheets
Project Report and Thesis contact
aravind.banakar@gmail.com
www.mbacasestudyanswers.com
ARAVIND – 09901366442 – 09902787224