The Value of Conducting Post-Marketing Clinical Research On Marketing Strategy Development
Nutraceutical Medical Research, LLC
By: Latesha Richards, Marketing Coordinator
WHAT IS THE DIFFERENCE BETWEEN PCD, GENERIC, AND ETHICAL PHARMA SECTORS?ambitbiomedix12
DIFFERENCE BETWEEN PCD, GENERIC, AND ETHICAL PHARMA SECTORS. Read More: https://bit.ly/2GFIONg
Are you a little bit confused about the difference between PCD, Generic, and Ethical Pharma Sectors? This blog gives the required information concisely and precisely.
Website: http://ambitbiomedix.com/
Social Media:
Facebook - https://www.facebook.com/ambitbiomedix/?ref=settings
Instagram - https://www.instagram.com/ambit_bio_medix/
Twitter - https://twitter.com/ambitbiomedix?lang=en
Linkedin - https://www.linkedin.com/company/ambit%E2%84%A2-bio-medix/about/
Youtube - https://www.youtube.com/watch?v=GPzB82AjvQA&t=3s
Biotech revolution changed the pharmaceutical industry, triggering a wave of risky collaborations between rivals. Based on the research findings, we answer the question why cooperation in the field of immuno-oncology is a better strategy for Pfizer and Merck KGaA, which aim to achieve competitive advantage quickly and with minimum effort. Combining their assets and core expertise companies realize benefits of greater size and variety in the conduct of research, development and commercializing of their new breakthrough therapy for cancer treatment.
WHAT IS THE DIFFERENCE BETWEEN PCD, GENERIC, AND ETHICAL PHARMA SECTORS?ambitbiomedix12
DIFFERENCE BETWEEN PCD, GENERIC, AND ETHICAL PHARMA SECTORS. Read More: https://bit.ly/2GFIONg
Are you a little bit confused about the difference between PCD, Generic, and Ethical Pharma Sectors? This blog gives the required information concisely and precisely.
Website: http://ambitbiomedix.com/
Social Media:
Facebook - https://www.facebook.com/ambitbiomedix/?ref=settings
Instagram - https://www.instagram.com/ambit_bio_medix/
Twitter - https://twitter.com/ambitbiomedix?lang=en
Linkedin - https://www.linkedin.com/company/ambit%E2%84%A2-bio-medix/about/
Youtube - https://www.youtube.com/watch?v=GPzB82AjvQA&t=3s
Biotech revolution changed the pharmaceutical industry, triggering a wave of risky collaborations between rivals. Based on the research findings, we answer the question why cooperation in the field of immuno-oncology is a better strategy for Pfizer and Merck KGaA, which aim to achieve competitive advantage quickly and with minimum effort. Combining their assets and core expertise companies realize benefits of greater size and variety in the conduct of research, development and commercializing of their new breakthrough therapy for cancer treatment.
Pharmacogenomics annotation in drug structured product labeling for clinical ...Richard Boyce, PhD
Prof. Boyce presents work on a semantic model for clinical pharmacogenomics statements in structured product labeling (SPLs) and how it can be integrated into clinical decision support.
See a video of the talk starting at 32:04 at the following link: http://videocast.nih.gov/summary.asp?Live=14776&bhcp=1
Commercial considerations in early drug developmentSunil Ramkali
It is important in the drug development process that marketers and researchers collaborate early to ensure that products being developed are truly innovative and deliver brand value to the different end users in a way that the product and the subsequent brand messaging is relevant, compelling and differentiating compared to the competition. T
In the market place that is heavily cost constraint, innovation is no longer about a unique mode of action or a new formulation, but more about the incremental brand value offered by new pharmaceutical products over existing treatments (standard of care) and how much healthcare systems are prepared to pay for these incremental benefits. My lecture at the Department of Innovation, Lund University, Sweden explored the importance of R&D functions getter closer to external stakeholders to really understand their needs, how they define brand value and the importance of considering this early in the drug development process.
Prof. Boyce discusses the "Linked SPLs" system its relationship to SPLs stored in DailyMed and the OpenFDA initiative. The talk will focus on the potential uses, strengths, and limitations Linked SPLs which represents drug product labeling as Semantic Web Linked Data.
Video of this talk can be found at the link below starting at starts at 3:11:26: http://videocast.nih.gov/summary.asp?Live=14776&bhcp=1
An overview of the research aims for the National Library of Medicine funded research project titled "Addressing gaps in clinically useful evidence on drug-drug interactions" (1R01LM011838-01)
To my mind, the cost of healthcare as it appears, is to a large extent, exaggerated by "frills" of the pharmaceutical companies in:
1.Packaging & cartoning for retail use. 2. Brand promotion among physicians to get brand-loyalty for specific prescriptions.
3.Salaries of drug representatives in large numbers to achieve personal friendships with physicians and thereby modulating their prescriptions!
4. Printing of large amount of promotion literature to act as education & reminders.
5.Organising expensive travel to physicians to exotic locations to win their favour of loyal prescriptions as a return for memorable experiences.
6.Gifts and souvenirs with personalized inscriptions !
Legal requirements for generics and abridged products and bioequivalenceinemet
PharmaCon2007 Congress, Dubrovnik, Croatia "New Technologies and Trends in Pharmacy, Pharmaceutical Industry and Education" http://www.pharmacon2007.com
Abstract is available at http://www.pharmaconnectme.com
Clinical Research is a most knowledge-intensive and interesting field in the pharmaceutical industry. There are more than 2, 50,000 positions unemployed in global Pharmaceutical industry.
Pharmacogenomics annotation in drug structured product labeling for clinical ...Richard Boyce, PhD
Prof. Boyce presents work on a semantic model for clinical pharmacogenomics statements in structured product labeling (SPLs) and how it can be integrated into clinical decision support.
See a video of the talk starting at 32:04 at the following link: http://videocast.nih.gov/summary.asp?Live=14776&bhcp=1
Commercial considerations in early drug developmentSunil Ramkali
It is important in the drug development process that marketers and researchers collaborate early to ensure that products being developed are truly innovative and deliver brand value to the different end users in a way that the product and the subsequent brand messaging is relevant, compelling and differentiating compared to the competition. T
In the market place that is heavily cost constraint, innovation is no longer about a unique mode of action or a new formulation, but more about the incremental brand value offered by new pharmaceutical products over existing treatments (standard of care) and how much healthcare systems are prepared to pay for these incremental benefits. My lecture at the Department of Innovation, Lund University, Sweden explored the importance of R&D functions getter closer to external stakeholders to really understand their needs, how they define brand value and the importance of considering this early in the drug development process.
Prof. Boyce discusses the "Linked SPLs" system its relationship to SPLs stored in DailyMed and the OpenFDA initiative. The talk will focus on the potential uses, strengths, and limitations Linked SPLs which represents drug product labeling as Semantic Web Linked Data.
Video of this talk can be found at the link below starting at starts at 3:11:26: http://videocast.nih.gov/summary.asp?Live=14776&bhcp=1
An overview of the research aims for the National Library of Medicine funded research project titled "Addressing gaps in clinically useful evidence on drug-drug interactions" (1R01LM011838-01)
To my mind, the cost of healthcare as it appears, is to a large extent, exaggerated by "frills" of the pharmaceutical companies in:
1.Packaging & cartoning for retail use. 2. Brand promotion among physicians to get brand-loyalty for specific prescriptions.
3.Salaries of drug representatives in large numbers to achieve personal friendships with physicians and thereby modulating their prescriptions!
4. Printing of large amount of promotion literature to act as education & reminders.
5.Organising expensive travel to physicians to exotic locations to win their favour of loyal prescriptions as a return for memorable experiences.
6.Gifts and souvenirs with personalized inscriptions !
Legal requirements for generics and abridged products and bioequivalenceinemet
PharmaCon2007 Congress, Dubrovnik, Croatia "New Technologies and Trends in Pharmacy, Pharmaceutical Industry and Education" http://www.pharmacon2007.com
Abstract is available at http://www.pharmaconnectme.com
Clinical Research is a most knowledge-intensive and interesting field in the pharmaceutical industry. There are more than 2, 50,000 positions unemployed in global Pharmaceutical industry.
Regulatory requirements for drug approval - industrial pharmacy IIJafarali Masi
Regulatory requirements for drug approval - industrial pharmacy IIDrug Development Teams, Non-Clinical Drug Development, Pharmacology, Drug Metabolism and Toxicology, General considerations of Investigational New Drug (IND) Application, Investigator’s Brochure (IB) and New Drug Application (NDA), Clinical research / BE studies, Clinical Research Protocols, Biostatistics in Pharmaceutical Product Development, Data Presentation for FDA Submissions, Management of Clinical Studies.
Post Marketing Surveillance and Pharmacoepidemiologyijtsrd
Post Marketing Surveillance PMS and pharmacoepidemiology are essential components of drug safety monitoring and effectiveness evaluation in real world clinical settings. PMS involves the continuous monitoring of pharmaceutical products after regulatory approval to detect and assess adverse events and safety issues that may not have surfaced during pre marketing clinical trials. Pharmacoepidemiology, on the other hand, employs epidemiological methods to study the effects of drugs in large populations, utilizing real world data from various sources. This article explores the significance of PMS and pharmacoepidemiology in ensuring patient safety, highlights their mutual contributions in research, and underscores the importance of collaborative efforts between regulatory agencies, academia, and pharmaceutical companies. The challenges related to data quality, privacy, and ethical considerations are discussed, along with potential advancements in methodologies and the integration of new technologies for future research and vigilance in drug safety and public health. Dr. Farheen Yousuf "Post-Marketing Surveillance and Pharmacoepidemiology" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-7 | Issue-4, August 2023, URL: https://www.ijtsrd.com/papers/ijtsrd59690.pdf Paper Url:https://www.ijtsrd.com/pharmacy/other/59690/postmarketing-surveillance-and-pharmacoepidemiology/dr-farheen-yousuf
In recognition of foot health month, the status of tea tree oil as an antimicrobial agent is reviewed. Tea tree oil shows great promise as an antifungal and antibacterial product. This includes topical infections of foot and toe nails.
Post Marketing Clinical Research & Marketing Strategy
1. The Value of Conducting Post
Post-Marketing Clinical Research On Marketing Strategy
arketing
Development
Nutraceutical Medical Research, LLC
By: Latesha Richards Marketing Coordinator
Richards,
Those of us who are marketing executives in the pharmaceutical industry acknowledge
the importance of post-marketing clinical research studies to further assess real-time use of a
marketing time
product. In an industry that is heavily regulated and scrutinized, pharmaceutical brands must not
,
only go through Phase I-III clinical research to validate the drug’s safety and tolerability in a
III
smaller subset of a diseased population, but testing of the product to monitor its safety and
effectiveness in a real-world setting once and after the product is approved for marketing. Post-
etting
marketing clinical research, used interchangeably with Phase IV testing, is a phase that takes
place after a product is available on the market for public use and is subsequently used to tr
track a
product’s safety and tolerability in a real
real-world setting. Marketers in this industry know that the
research needed to market and sell a drug product is quite different than research needed to gain
the Food & Drug Administration’s (
(FDA) approval.1 In addition to post-marketing surveillance,
marketing
Phase IV clinical studies are also helpful in d
developing marketing strategy for a product. Post-
marketing research gives insight into all kinds of questions and concerns raised by the FDA. Not
only does it allow companies to monitor for real time effectiveness, long term safety and
real-time
tolerability, but it may also give rise to evidence of possible new indications and new markets for
which the drug product had not been initially approved. Just as Phase IV clinical r
ust research is
1
Desphande, Ravi, PharmD, Bridging the Gap between Clinical and Marketing Initiatives; Canadian Pharmaceutical Marketing, spring 2003 p39.
Initiatives; 2003,
1
2. used for conventional pharmaceutical medicines it is just as important and should be equally
medicines,
important in the research phase of a natural product such as nutraceuticals, botanicals and dietary
supplements.
The ecessity for Phase IV Research
Talking about Phase IV research raises the question as to why it is needed in the first
place. Before drugs are marketed, drugs are considered drug candidates. During Phases I, II,
and III of the drug candidate’s life cycle, clinical research is designed to test and validate how
safe and effective it is. As you know, these processes can take many, many years, filled with
many trials and errors. If a drug can
candidate has successfully sustained this and makes it way to
market, and becomes a drug product, the are many important and unanswered questions that
there
are, in essence, very time-sensitive. These questions include mainly safety and efficacy concerns
sensitive.
by the FDA: how safe and effective is the drug’s use in a diseased population with varying
:
degrees of illness? How safe and effective is it when used by a patient with more than one illness
ness?
or those taking multiple drugs? How does the drug product compare in safety, efficacy and
safety,
tolerability with other products in its class? What are the risks vs. benefits of the drug? Do the
benefits outweigh the risks? Companies who face the daily challenges of answering these
ompanies wering
questions depend on the conduct of post
uct post-approval research for answers. Second, they see the
importance of working with their medical co
counterparts to access such data and create a
transparent decision-making process 2 Accessible clinical data makes it possible for a company
making process.
to quickly and effectively answer post
post-approval FDA questions and may make a difference
2
Best Practices LLC, Report Summary - Launching Pharmaceutical Megabrands: Best Practices in Marketing Blockbusters 2004 Edition p2, accessed at
Edition,
http://www3.best-in-class.com/
2
3. between market success and failure of the product.3 But these questions must also be dealt with
by marketers when strategizing a marketing plan targeted to its primary market. In the
pharmaceutical industry, time equals money, indeed.
The Value of Clinical Research
You may be asking, “What value does clinical research have on marketing the product?
What e product?”
The value is tremendous, to say the least. In the pharmaceutical world, clinical research is the
one of the bridges to the gap in marketing ( other being marketing research) namely between
(the
the product and customer. Richard K. Thomas defines marketing as “the process of planning and
executing the [product] conception, pricing, promotion and distribution [place] of ideas, goods,
and services to create exchanges… 4 between the customer and buyer. This is essentially
exchanges…,”
referred to as the four (4) P’s of marketing (product, price, promotion, and place). By answering
place)
many unknowns about the drug (mentioned earlier) many insights and analytics regarding the
earlier),
product, price, promotion, and place can be drawn to develop marketing strategies to essentially
trategies
connect the product with the customer. The role of clinical research in marketing medicines is to
aid that connection. What makes ma
marketing medicines so uniquely different from other product
marketing is that the FDA is the intermediary. The FDA decides the fate of a drug candidate or
keting
product entering the marketplace based on the supporting clinical evidence presented by the
company and gives the final ‘yea or nay. Pharmaceutical companies are obligated under the
yea nay.’
Pharmaceutical Research and Manufacturers of America (PhRMA) code to be informative,
3
EMC Perspective, Leveraging the Value of Data from Clinical Trials Accessed at http://www.emc.com/collateral/emc-perspective/h4338
ue Trials, perspective/h4338-clinical-trials-ep.pdf
4
Thomas, Richard K. Health Services Marketing: A Practitioner’s Guide New York: Springer Science & Business Media, LLC, 2008.
Guide;
3
4. ethical and professional when marketing medicines to physicians.5 Clinical research essentially
represents those three. Clinical research takes out the risk of compromising patient care when
presenting information and educating clinicians about a drug’s use and health benefits. It
provides the hard scientific evidence needed in order for healthcare professionals to make sound
and informed decisions about medical treatment for their patients. The company’s commitment
bout
to medical research also makes the company more trustworthy to the medical community.
Companies who utilize clinical research data can also benefit from the tons of insight into how a
product is different from others indicated to t
treat the same illness(es), what its attributes are
compared with competing brands how a product should be competitively positioned based on its
brands,
attributes, how a company should promote the product to its primary constituents, e.g.
physicians, patients and payer organizations (health plans and insurance companies) etc.
companies),
Clinical research plays a huge role in formulating marketing strategy, as the data gives insight
linical
into customer/consumer needs and competitive positioning, and also what aspect of the drug
/consumer lso
product’s profile should be emphasized when targeting marketing campaigns to key customers
and consumers.6
How Clinical Research Can Be Used A a Dissemination & Education Tool to Key Target
inical As
Groups
5
Pharmaceutical Research & Manufacturers of America: Code on Interactions with Healthcare Professionals. Access on March 20, 2009, at
Accessed
http://www.phrma.org/files/PhRMA%20Marketing%20Code%202008.pdf
6
Best Practices LLC, Report Summary - Launching Pharmaceutical Megabrands: Best Practices in Marketing Blockbusters 2004 Edition p2, accessed at
Practices Edition,
http://www3.best-in-class.com/ .
4
5. Clinical research data provides the most up-to-date scientific intelligence on the product’s
date
mechanism of action, effectiveness and safety profile to key groups and decision
decision-makers. Those
key target groups and decision makers include physicians, payers, buyers, key opinion leaders
(KOLs), the company’s sales force and even the FDA. It is important for the pharmaceutical
industry as an educational tool for and information dissemination to their primary constituents in,
r
but not limited to these aspects:
1. Physicians: It is ideal, especially for pharmaceutical companies that healthcare
,
professionals base their prescribing decisions on supporting evidence provided by clinical
data,7 however, healthcare professionals are expected to base their patient care “solely on
each patient’s medical needs and their medical knowledge and experience.”8 The PhRMA
code also reinforces that professional exchanges with the medical community is designed
to benefit patients and enhance the overall medical practice. Thus, there is great
opportunity for companies to interact with physicians and provide scientific and
ies
educational information as well as medical education through clinical research. The
education
more robust the clinical evidence, the better the case is for that drug to be on top of mind
better
when a physician is making a prescribing decision. Building professional relationships
with the medical community is critical for these companies because it opens up
opportunity for life altering products to be accessible to patients who need them and
subsequently earn more return on investment.
7
Maxwell, Simon R J Evidence based medicine is the goal, but prescribers still need education, experience, and common sense; BMJ 2005;331:247
2005;331:247-248.
8
Pharmaceutical Research & Manufacturers of America: Code on Interactions with Healthcare Professionals. Access on March 20, 2009, at
http://www.phrma.org/files/PhRMA%20Marketing%20Code%202008.pdf
5
6. 2. Payers: A payer’s responsibility is to provide healthcare that is effective, affordable and
satisfactory to as many people as possible. When new products have entered the market,
payers (healthcare insurance providers are primarily concerned with 1). Evidence that
healthcare providers)
demonstrates a product’s clinical safety and effectiveness; 2). Cost-effectiveness – payers
effectiveness
need to know and be reassured
reassured“…that their dollars are being spent wisely”9 and; 3). How
clinical research findings can be translated to medical practice from a disease prevention
and management perspective 10 Findings from traditional clinical trial research are
perspective.
paramount for health plans in addressing and determining all of the above concerns.
termining
However in today’s medical culture where the paradigm has shifted from the physician to
the patient, health plan companies see the need to become more patient-centered and to
centered
shift the way in which they provide care. Representatives from major hea plan
health
companies have argued that more non-traditional clinical research needs to be available,11
traditional
especially when it is time to make crucial decisions around how to effectively deliver
healthcare, what services to cover and r
recommend to the insured. That is to say more
research needs to be focused and done around the patient. These include behavioral
research on physicians in a clinical setting and how to change their behavior, health
change
services research that looks at ways in which to improve the delivery of healthcare and
healthcare,
9
Tunis, Sean, Korn, Allan, and Ommaya, Alex, The Role of Purchasers and Payers in the Clinical Research Enterprise: Based on a Workshop of the Clinical
Research Roundtable; Board on Health Sciences Policy, 2002, p30
icy, p30.
10
Tunis, Sean, Korn, Allan, and Ommaya, Alex, The Role of Purchasers and Payers in the Clinical Research Enterprise: Based on a Workshop of the Clinical
Research Roundtable; Board on Health Sciences Policy, 2002, p29
alth p29.
11
Tunis, Sean, Korn, Allan, and Ommaya, Alex, The Role of Purchasers and Payers in the Clinical Research Enterprise: Based on a Workshop of the Clinical
Research Roundtable; Board on Health Sciences Policy, 2002, p
; p29-37.
6
7. other forms of public health and outcomes research.12 This presents huge opportunities
for pharmaceutical companies to work with in-house and external researchers to fund and
house
spearhead these kinds of research to address these concerns.
3. KOLs: Effectively marketed clinical data to KOLs is a huge factor in gaining full product
support going forward. A crucial demographi KOLs are expert physicians who have
demographic,
influence over medical practice. They must be a well sought out group for the
pharmaceutical industry because they “set the pace for industry trends.”13 They can share
a wealth of information and insight “ranging from clinical science to advertising
concepts” and provide “highly credible exposure for a product in the medical community
through speaking engagements, articles in medical journals and general practice.”14
Engaging them in qualitative market research and more importantly medical symposiums
more
with the latest clinical research early and throughout the product’s lifecycle could mean
invaluable feedback and insight throughout the life of a product and thus increased
marketing exposure in clinical practice.
4. Sales Team: Although not a target group the sales force must nonetheless be a number
: group,
one priority for any company engaging in direct to physician sales to their target market.
The sales team essentially acts as the spokesperson between the company/product and t
the
physician, thus time must be invested to proactively and continuously keep members of
12
Tunis, Sean, Korn, Allan, and Ommaya, Alex, The Role of Purchasers and Payers in the Clinical Research Enterprise: Based on a Wor
Workshop of the Clinical
Research Roundtable; Board on Health Sciences Policy, 2002, p29
; p29-37.
13
Schwebach, Gary, MD, Qualitative Market Landscaping Helps Pharma Grow Better Brands http://www.gs-research.com/pdf/QRCAWinter
Brands, research.com/pdf/QRCAWinter-Pharma.pdf, Winter
2007, p2.
14
Schwebach, Gary, MD, Qualitative Market Landscaping Helps Pharma Grow Better Brands http://www.gs-research.com/pdf/QRCAWinter
Brands, QRCAWinter-Pharma.pdf, Winter
2007, p2.
7
8. the sales force educated on the benefits of the product. Clinical research provides the
company's sales force with newest data to go out and effectively disseminate a educate
and
physicians on the product. The degree of success of the pharmaceutical company’s sales
product.
team directly influences the revenue generated for the company and the longevity of the
brand.
5. Buyers: Clinical research is and will have increasing importance for distributors when
:
helping consumers understa labels and products. With increasing consumer demand
understand
for natural products, there is more need for in
in-store nutrition knowledge with the retail
within
sector. Retailers must be well
etailers well-informed about the products they distribute and sell.
he
Before point-of-sale, retailers have an important role in explaining nutrition labels to
sale,
consumers. This presents loads of opportunity for natural product suppliers to utilize
clinical research, in conjunction with market and outcomes research to train and educate
market
their distributors using their product’s clinical trial data. Opportunities such as
advertising displays, promotional items, leaflets, pamphlets, videos, etc. can be used by
distributors so in turn they can market to their consumers.
6. FDA: Clinical research also serves as a dissemination tool to provide evidence to the
:
FDA when a pharmaceutical company is interested in expanding a drug’s clinical
indications (another condition that the drug can treat that is different from the
is
condition(s) it was initially approved for). If the drug product is fortunate to have such
additional benefits, it can open up a whole new market, and thus yield increased product
value and the potential of limitless return on investm
investment.
8
9. Post-Marketing Research - Pharmaceuticals vs. atural Products : Similarities &
Differences
You may be asking, how pharmaceutical post-marketing clinical research compare with
compares
post-marketing research for natural products having health benefit indications. Post
Post-marketing
research will answer similar, if not the same, types of questions. Sure, the FDA approval process
nswer
is very different for natural products, there is no Phase I – Phase III product lifecycle per se, but
the marketing success of the natural product industry like any other industry, is influenced by
industry,
the product, price, promotion and place that marketing strategy is designed to address The
address.
stakeholders for the natural products industry remains the same as for pharmaceutical, e.g.
consumers (patients), physicians and/or complimentary health professionals (naturopathic,
holistic, homeopathic, herbal practitioners, etc.) and buyers, with slight emphasis on one market
practitioners,
over the other. Each of these groups still must be tapped into and convinced in the post-
marketing phase of the product with clinical data to get their acceptance, buy-in, and ultimately,
their sales.
It is no surprise that Phase IV clinical research has become the fastest growing are of
area
clinical research today.15 It is such a major part of the pharmaceutical drug commercialization
process because of the questions that the clinical data will answer for the FDA, but also because
of the many opportunities it creates to effectively market to physicians, patients, payers, buyers,
ients,
KOLs, the sales team and the FDA The same goes for dietary supplements and other
FDA.
nutraceuticals with health claims. In a growing industry that is saturated with competition,
.
15
Cutting Edge Information. Mastering Phase IV Clinical Trials. Accessed on March 18, 2009, at http://www.cuttingedgeinfo.com/postmarketingtrials/
9
10. where consumers are inundated with choices, and where there are too many channels of product
choices,
distribution available, clinical research becomes paramount in distinguishing a product from its
competition, strategically positioning the product against the standard, and enhancing the
product’s attributes, among others
, others.
utraceutical Medical Research, LLC is the only dedicated, full-service, nutraceutical
service, nutraceutical-focused
contract (clinical) research organization. We serve the natural product, dietary supplement,
nutraceutical, cosmeceutical and pharmaceutical industries.
utical, MR will help, 1. Differentiate
your product in the marketplace; 2. Enhance your product’s sustainability; 3. Increase your
ROI; 4. Meet your goals for attracting new buyers and users; 5. Strategically position your
product and brand.
To find out more about how post-
-marketing clinical research can help increase your product
value and the specific types of research that can be done for your particular product, please
contact us at:
10
11. REFERE CES
1. Desphande, Ravi, PharmD. Bridging the Gap between Clinical and Marketing Initiatives
Initiatives;
Canadian Pharmaceutical Marketing, spring 2003, p39.
2. Best Practices LLC, Report Summary - Launching Pharmaceutical Megabrands: Best
Practices in Marketing Blockbusters 2004 Edition p2, accessed at http://www3.best
Edition, http://www3.best-in-
class.com/
3. EMC Perspective, Leveraging the Value of Data from Clinical Trials Accessed at
Trials,
http://www.emc.com/collateral/emc
om/collateral/emc-perspective/h4338-clinical-trials-ep.pdf
ep.pdf
4. Thomas, Richard K. Health Services Marketing: A Practitioner’s Guide New York:
Guide;
Springer Science & Business Media, LLC, 2008.
5. Pharmaceutical Research & Manufacturers of America: Code on Interaction with
Interactions
Healthcare Professionals. Accessed on March 20, 2009, at
http://www.phrma.org/files/PhRMA%20Marketing%20Code%202008.pdf
6. Maxwell, Simon R J Evidence based medicine is the goal, but prescribers still need
education, experience, and common sense; BMJ 2005;331:247-248.
7. Tunis, Sean, Korn, Allan, and Ommaya, Alex, The Role of Purchasers and Payers in the
Clinical Research Enterprise: Based on a Workshop of the Clinical Research
Roundtable; Board on Health Sciences Policy, 2002, p29
; p29-37.
8. Schwebach, Gary, MD, Qualitative Market Landscaping Helps Pharma Grow Better
Brands, http://www.gs-research.com/pdf/QRCAWinter
research.com/pdf/QRCAWinter-Pharma.pdf, winter 2007, p2.
9. Cutting Edge Information. Mastering Phase IV Clinical Trials. Accessed on March 18,
2009, at http://www.cuttingedgeinfo.com/postmarketingtrials/
11