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New Pharma Magazine is holding its launch party in New York City on March 14th during DCAT Week. The magazine is the premier source for news, events, and lifestyle insights for decision makers in the pharmaceutical industry. Key industry leaders such as Ed Borkowski and Stu Williams will attend the exclusive cocktail event at the W Hotel New York along with the president of Generic Pharma 2.0. New Pharma Magazine focuses on engaging readers on strategic issues facing the changing pharmaceutical industry.
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New Pharma Magazine Launch Party in NYC!
New Pharma Magazine is holding its launch party in New York City on March 14th during DCAT Week. The magazine is the premier source for news, events, and lifestyle insights for decision makers in the pharmaceutical industry. Key industry leaders such as Ed Borkowski and Stu Williams will attend the exclusive cocktail event at the W Hotel New York along with the president of Generic Pharma 2.0. New Pharma Magazine focuses on engaging readers on strategic issues facing the changing pharmaceutical industry.
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- Business Development Toolkit
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GP20 Licensing Pavillion 2012 Coexhibitor Kit
The document is a promotional kit for co-exhibitors at a pharmaceutical licensing pavilion at a trade show. It highlights the benefits of exhibiting collaboratively at the pavilion such as increased networking opportunities and return on investment compared to exhibiting alone. It describes the location and facilities of the pavilion including private meeting rooms and networking areas. Floor plans of the pavilion layout are also included showing the arrangement of the different networking stations.
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The document discusses challenges and opportunities in the development of biosimilars. It provides perspectives from several industry experts on the top hurdle being a lack of clarity around intellectual property and marketing strategies as well as high development costs. The experts note that developing the necessary skill sets around quality by design, analytics, and clinical trial design is key to overcoming hurdles in developing biosimilars safely and effectively.
Your Ideal Pfizer
Pfizer is facing significant challenges as many of its blockbuster drug patents expire in the coming years. This will open the door for cheaper generic competition that will eat into Pfizer's revenues. As CEO, I would [1] focus R&D on developing new blockbuster drugs to replace revenue losses, [2] look for strategic acquisitions of companies with promising drug pipelines, and [3] strengthen Pfizer's portfolio of treatments for chronic diseases to take advantage of demographic trends. With successful execution of these strategies, Pfizer could remain the world's most valued pharmaceutical company.
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OTC Licensing Product Portfolio
This document provides information on various over-the-counter licensing products categorized by therapeutic class and approval type. It includes summaries of cosmetic and medical device products for skin care, feminine hygiene, and fertility testing. Products like the Nanodermix Nanoanti-Age cream, nSkin wrinkle treatments, Esui feminine wash, Donna fertility tester, Donna Glove, and Multi-Gyn vaginal health products are highlighted.
LinkedIn Survey Results
This document contains 3 short summaries:
1) It summarizes statistics on how people access information online, with most using search engines and some using social media.
2) It summarizes statistics on people's concerns about data privacy when using different methods to access information online.
3) It summarizes statistics on how people recognize technology companies, with most recognizing Google and some recognizing other large companies.
New Pharma Magazine
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Look for the pre-launch edition coming in December 2011!
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Wörwag Research and Development GmbH is a subsidiary of Wörwag Pharma Group dedicated to developing generic, OTC, and new chemical entity products and medical devices according to European guidelines. Its business model involves licensing out its developed products in Europe and worldwide. The document provides readily compiled dossiers for several generic drug products that have received German and European marketing authorizations and are available for submission in other markets. It also outlines ongoing development projects and provides contact information.
Neogen presentation april_2011_gl
This confidential presentation from Neogen in April 2011 discusses their API development and product selection process. Neogen develops and licenses out pharmaceutical products to generic companies wishing to expand their portfolios but lacking skills or willingness to undertake development. Their development process includes market intelligence, formulation, manufacturing facilities selection, regulatory strategy, and clinical testing for some products. They have first mover advantage on several products launched via various dosage forms developed both in-house and through production partners in Europe. Key personnel are introduced with relevant experience in the pharmaceutical industry.
Genericlicensing.com - featured companies 2011
This document summarizes Astron Research Ltd, a featured developer in the Global Generic Product Directory. Astron is an Indian pharmaceutical company established in 2001 that develops and manufactures generic pharmaceutical products. It has dossiers for over 100 molecules ready or in development for global markets. Astron has capabilities across the pharmaceutical value chain including API manufacturing, finished dose production, marketing and distribution. It is seeking partnerships for product development and commercialization.
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This document is the 3rd edition of the Global Generic Product Directory, which contains information on generic pharmaceutical products and their developers. It has more products, developers, and data than previous editions. The directory aims to help users license generic products by providing contact information for developers. It can be accessed online for the latest product and company information. The founder of Genericlicensing Limited, which created the directory, encourages users to provide feedback on how to improve the resource.
Heal gel presentation
Healgel is an innovative skin care gel developed by UK plastic surgeons to promote skin healing and reduce scar appearance. It contains ingredients that soothe, repair, and prevent scarring. A survey of 141 people found that 94% reported Healgel was very soothing, 82% had reduced swelling, and 85% found it highly effective at reducing discoloration. The gel's effectiveness comes from ingredients that stimulate collagen production, encourage cell renewal, seal the skin surface, and reduce itching and puffiness. Users reported the gel helped scars heal quickly and comfortably and reduced acne scarring.
Biosimilars - analysing market intelligence (Peter Wittner)
This document summarizes a presentation about analyzing the biosimilars market. It discusses how interchangeability is a major hurdle for biosimilar uptake compared to generics. It analyzes growth statistics for the biologics market and shows it is concentrated in western markets, while most of the world's population is in developing markets. Future opportunities for biosimilars growth are seen in the US, EU, and India due to factors like pricing pressures and market entry barriers. Key therapeutic areas and where to invest are also discussed.
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The document discusses a joint project between GlaxoSmithKline, GEA Pharma Systems, and Siemens to develop a continuous manufacturing solution for tablet production. The project was completed in just six months and proved that continuous manufacturing can produce tablets continuously and reliably with real-time quality monitoring. This approach uses significantly less space than traditional batch processes and improves manufacturing efficiency. The success of the project demonstrated that continuous manufacturing has potential to transform pharmaceutical production.
Generic Licensing Pavillion @ CPhI WW 2011
This document proposes a licensing-focused pavilion at the CPhI Worldwide Frankfurt trade show in October 2011. [1] The pavilion would promote licensing companies together to attract more clients than exhibiting individually. [2] Exhibiting in the pavilion would provide marketing and promotion for 12 months before and after the show as well as on-site support like catering and meetings with top clients. [3] Companies interested in the pavilion must be involved in licensing and book space soon as places are limited.
Opportunities and barriers in the biosimilar marketevolution or revolution fo...
This document discusses the opportunities and barriers in the biosimilar drug market. While biosimilars could generate billions in sales, their development faces significant challenges compared to traditional generics. Biosimilars are biologic drugs whose development requires clinical testing due to variations in production, unlike traditional generics. Their high development costs of $10-40 million mean price discounts must be smaller. Physicians may also be cautious to adopt biosimilars. For generics companies to succeed in biosimilars, they will need to adopt new business models focused on marketing and distribution, rather than frequent low-cost drug launches. The top biosimilar targets are expected to be erythropoietin, G-CSF, interferons,
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Patent Portfolio Sale: Fosphenytoin and Propofol
The document describes the sale of Cydex Pharmaceuticals' patent portfolio covering two Captisol-enabled drug products: Captisol-enabled fosphenytoin and Captisol-enabled propofol. Captisol is a modified cyclodextrin that improves drug solubility, stability, and bioavailability. The fosphenytoin product offers room temperature storage compared to refrigeration required for the marketed product. The propofol product has enhanced stability and reduces pain, allergic responses, and microbial contamination compared to existing formulations. The portfolio includes two issued US patents and fifteen foreign counterparts covering the drug compositions and methods of making them.
Woerwag R&D presentation Dec 2010
Wörwag R&D GmbH is a subsidiary of Wörwag Pharma Group dedicated to developing generic and over-the-counter drugs according to European guidelines. Their mission is to develop a range of generics and OTC products to launch upon patent expiry. They have readily compiled dossiers for several products that have received German and some European marketing authorizations. They are currently developing dossiers for products including candesartan, candesartan-HCT, donepezil, galantamine, levetiracetam, pioglitazon, and valsartan.
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Pfizer is facing significant challenges as many of its blockbuster drug patents expire in the coming years. This will open the door for cheaper generic competition that will eat into Pfizer's revenues. As CEO, I would [1] focus R&D on developing new blockbuster drugs to replace revenue losses, [2] look for strategic acquisitions of companies with promising drug pipelines, and [3] strengthen Pfizer's portfolio of treatments for chronic diseases to take advantage of demographic trends. With successful execution of these strategies, Pfizer could remain the world's most valued pharmaceutical company.
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An article featured in our new New Pharma Magazine to be released in February. Stay tuned for details on how to subscribe to this cutting edge industry publication.
OTC Licensing Product Portfolio
This document provides information on various over-the-counter licensing products categorized by therapeutic class and approval type. It includes summaries of cosmetic and medical device products for skin care, feminine hygiene, and fertility testing. Products like the Nanodermix Nanoanti-Age cream, nSkin wrinkle treatments, Esui feminine wash, Donna fertility tester, Donna Glove, and Multi-Gyn vaginal health products are highlighted.
LinkedIn Survey Results
This document contains 3 short summaries:
1) It summarizes statistics on how people access information online, with most using search engines and some using social media.
2) It summarizes statistics on people's concerns about data privacy when using different methods to access information online.
3) It summarizes statistics on how people recognize technology companies, with most recognizing Google and some recognizing other large companies.
New Pharma Magazine
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Look for the pre-launch edition coming in December 2011!
content@genericlicensing.com if you're interested in contributing editorial content, advertisement and/or advertorials.
Woerwag RD presentation
Wörwag Research and Development GmbH is a subsidiary of Wörwag Pharma Group dedicated to developing generic, OTC, and new chemical entity products and medical devices according to European guidelines. Its business model involves licensing out its developed products in Europe and worldwide. The document provides readily compiled dossiers for several generic drug products that have received German and European marketing authorizations and are available for submission in other markets. It also outlines ongoing development projects and provides contact information.
Neogen presentation april_2011_gl
This confidential presentation from Neogen in April 2011 discusses their API development and product selection process. Neogen develops and licenses out pharmaceutical products to generic companies wishing to expand their portfolios but lacking skills or willingness to undertake development. Their development process includes market intelligence, formulation, manufacturing facilities selection, regulatory strategy, and clinical testing for some products. They have first mover advantage on several products launched via various dosage forms developed both in-house and through production partners in Europe. Key personnel are introduced with relevant experience in the pharmaceutical industry.
Genericlicensing.com - featured companies 2011
This document summarizes Astron Research Ltd, a featured developer in the Global Generic Product Directory. Astron is an Indian pharmaceutical company established in 2001 that develops and manufactures generic pharmaceutical products. It has dossiers for over 100 molecules ready or in development for global markets. Astron has capabilities across the pharmaceutical value chain including API manufacturing, finished dose production, marketing and distribution. It is seeking partnerships for product development and commercialization.
2011 Global Generic Product Directory Demo
This document is the 3rd edition of the Global Generic Product Directory, which contains information on generic pharmaceutical products and their developers. It has more products, developers, and data than previous editions. The directory aims to help users license generic products by providing contact information for developers. It can be accessed online for the latest product and company information. The founder of Genericlicensing Limited, which created the directory, encourages users to provide feedback on how to improve the resource.
Heal gel presentation
Healgel is an innovative skin care gel developed by UK plastic surgeons to promote skin healing and reduce scar appearance. It contains ingredients that soothe, repair, and prevent scarring. A survey of 141 people found that 94% reported Healgel was very soothing, 82% had reduced swelling, and 85% found it highly effective at reducing discoloration. The gel's effectiveness comes from ingredients that stimulate collagen production, encourage cell renewal, seal the skin surface, and reduce itching and puffiness. Users reported the gel helped scars heal quickly and comfortably and reduced acne scarring.
Biosimilars - analysing market intelligence (Peter Wittner)
This document summarizes a presentation about analyzing the biosimilars market. It discusses how interchangeability is a major hurdle for biosimilar uptake compared to generics. It analyzes growth statistics for the biologics market and shows it is concentrated in western markets, while most of the world's population is in developing markets. Future opportunities for biosimilars growth are seen in the US, EU, and India due to factors like pricing pressures and market entry barriers. Key therapeutic areas and where to invest are also discussed.
GSK and Siemens continuous tablet manufacture
The document discusses a joint project between GlaxoSmithKline, GEA Pharma Systems, and Siemens to develop a continuous manufacturing solution for tablet production. The project was completed in just six months and proved that continuous manufacturing can produce tablets continuously and reliably with real-time quality monitoring. This approach uses significantly less space than traditional batch processes and improves manufacturing efficiency. The success of the project demonstrated that continuous manufacturing has potential to transform pharmaceutical production.
Generic Licensing Pavillion @ CPhI WW 2011
This document proposes a licensing-focused pavilion at the CPhI Worldwide Frankfurt trade show in October 2011. [1] The pavilion would promote licensing companies together to attract more clients than exhibiting individually. [2] Exhibiting in the pavilion would provide marketing and promotion for 12 months before and after the show as well as on-site support like catering and meetings with top clients. [3] Companies interested in the pavilion must be involved in licensing and book space soon as places are limited.
Opportunities and barriers in the biosimilar marketevolution or revolution fo...
This document discusses the opportunities and barriers in the biosimilar drug market. While biosimilars could generate billions in sales, their development faces significant challenges compared to traditional generics. Biosimilars are biologic drugs whose development requires clinical testing due to variations in production, unlike traditional generics. Their high development costs of $10-40 million mean price discounts must be smaller. Physicians may also be cautious to adopt biosimilars. For generics companies to succeed in biosimilars, they will need to adopt new business models focused on marketing and distribution, rather than frequent low-cost drug launches. The top biosimilar targets are expected to be erythropoietin, G-CSF, interferons,
Hetero Europe company presentation 2010
Hetero is a global pharmaceutical company that develops, manufactures and markets APIs, intermediates, and finished dosage forms. It has 18 manufacturing facilities across 11 countries with 6000 employees worldwide. The facilities meet cGMP standards and are approved by major regulatory bodies. Hetero produces over 200 APIs and a wide range of finished dosage forms for over 100 countries.
Patent Portfolio Sale: Fosphenytoin and Propofol
The document describes the sale of Cydex Pharmaceuticals' patent portfolio covering two Captisol-enabled drug products: Captisol-enabled fosphenytoin and Captisol-enabled propofol. Captisol is a modified cyclodextrin that improves drug solubility, stability, and bioavailability. The fosphenytoin product offers room temperature storage compared to refrigeration required for the marketed product. The propofol product has enhanced stability and reduces pain, allergic responses, and microbial contamination compared to existing formulations. The portfolio includes two issued US patents and fifteen foreign counterparts covering the drug compositions and methods of making them.
Woerwag R&D presentation Dec 2010
Wörwag R&D GmbH is a subsidiary of Wörwag Pharma Group dedicated to developing generic and over-the-counter drugs according to European guidelines. Their mission is to develop a range of generics and OTC products to launch upon patent expiry. They have readily compiled dossiers for several products that have received German and some European marketing authorizations. They are currently developing dossiers for products including candesartan, candesartan-HCT, donepezil, galantamine, levetiracetam, pioglitazon, and valsartan.
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