Libby Baney, Executive Director for the Alliance for Safe Online Pharmacies talks about the current state of rogue online pharmacies and efforts to curb them.
I have been working on the topic of anti-counterfeiting for a number of years and find myself increasingly engrossed and thoroughly surprised as our understanding of this topic grows. The imagination and the brutality with which the criminal industry produces, distributes and sells imitation goods is unmatched. The consequences of such dire acts are not only killing children but also affecting the lives of many and fighting such forgery has become a personal battle for me.
Counterfeit drugs pose a major global problem and public health risk. According to the World Health Organization, over half of counterfeit drug cases found no active ingredients, while others contained incorrect or dangerous ingredients. Developing countries are especially impacted, with up to 60% of reported counterfeit drugs. Counterfeiting undermines healthcare systems and can have deadly consequences. The document warns that weak drug regulation and an unsecured supply chain allow for counterfeits to proliferate. It advocates purchasing from authorized drug distributors only to help strengthen oversight of the pharmaceutical supply system.
Public Opinion On Prescription Drugs And Their PricesKFF
- According to polls from 2015-2019, around 6 in 10 Americans currently take at least one prescription medication and 1 in 4 take 4 or more. While most say the cost of prescription drugs is unreasonable, around 3 in 4 currently taking medications say affording them is easy. However, those taking more medications report more cost problems.
- Around 3 in 10 Americans have not taken their medication as prescribed at some point due to costs, such as not filling a prescription, cutting pills in half, or taking over-the-counter drugs instead.
- Majorities of the public favor policies to lower drug costs like requiring list prices in ads, easier generics, and government negotiations. However, views on the best approach vary by
Prescription Medicines Costs in Context May 2020PhRMA
This document discusses prescription drug costs and spending in the United States. It notes that while 56 new medicines were approved by the FDA in 2019, out-of-pocket costs for patients continue to rise. While overall spending on prescription drugs grew by just 2.5% in 2018, nearly half of brand drug spending goes to entities other than the manufacturers. The document also compares US drug costs and availability to other countries.
This document summarizes pharmaceutical research and development in Minnesota. It notes that 19 products are currently in active clinical development with the FDA. The top five therapy areas for ongoing clinical trials by Minnesota entities are oncology, central nervous system disorders, anti-infectives, cardiovascular disorders, and endocrine disorders. Minnesota's current FDA approval pipeline includes pre-clinical and phase 1, 2, and 3 clinical trials. The top three companies conducting these trials are the University of Minnesota, Mayo Clinic, and 3M.
In this presentation, Director of National Outreach Shabbir Imber Safdar reviews the current state of counterfeit drugs in America today, discusses some of the myths surrounding importation, and provides tips for saving money safely on the cost of prescription drugs.
The antibody service and more efficient processesbostonmol
Boston Molecules contain Antibody services and Base editing which is growing at compound annual rate since 2014 contain biopharmaceutical products which become more dynamic and rapidly expanding in market.
I have been working on the topic of anti-counterfeiting for a number of years and find myself increasingly engrossed and thoroughly surprised as our understanding of this topic grows. The imagination and the brutality with which the criminal industry produces, distributes and sells imitation goods is unmatched. The consequences of such dire acts are not only killing children but also affecting the lives of many and fighting such forgery has become a personal battle for me.
Counterfeit drugs pose a major global problem and public health risk. According to the World Health Organization, over half of counterfeit drug cases found no active ingredients, while others contained incorrect or dangerous ingredients. Developing countries are especially impacted, with up to 60% of reported counterfeit drugs. Counterfeiting undermines healthcare systems and can have deadly consequences. The document warns that weak drug regulation and an unsecured supply chain allow for counterfeits to proliferate. It advocates purchasing from authorized drug distributors only to help strengthen oversight of the pharmaceutical supply system.
Public Opinion On Prescription Drugs And Their PricesKFF
- According to polls from 2015-2019, around 6 in 10 Americans currently take at least one prescription medication and 1 in 4 take 4 or more. While most say the cost of prescription drugs is unreasonable, around 3 in 4 currently taking medications say affording them is easy. However, those taking more medications report more cost problems.
- Around 3 in 10 Americans have not taken their medication as prescribed at some point due to costs, such as not filling a prescription, cutting pills in half, or taking over-the-counter drugs instead.
- Majorities of the public favor policies to lower drug costs like requiring list prices in ads, easier generics, and government negotiations. However, views on the best approach vary by
Prescription Medicines Costs in Context May 2020PhRMA
This document discusses prescription drug costs and spending in the United States. It notes that while 56 new medicines were approved by the FDA in 2019, out-of-pocket costs for patients continue to rise. While overall spending on prescription drugs grew by just 2.5% in 2018, nearly half of brand drug spending goes to entities other than the manufacturers. The document also compares US drug costs and availability to other countries.
This document summarizes pharmaceutical research and development in Minnesota. It notes that 19 products are currently in active clinical development with the FDA. The top five therapy areas for ongoing clinical trials by Minnesota entities are oncology, central nervous system disorders, anti-infectives, cardiovascular disorders, and endocrine disorders. Minnesota's current FDA approval pipeline includes pre-clinical and phase 1, 2, and 3 clinical trials. The top three companies conducting these trials are the University of Minnesota, Mayo Clinic, and 3M.
In this presentation, Director of National Outreach Shabbir Imber Safdar reviews the current state of counterfeit drugs in America today, discusses some of the myths surrounding importation, and provides tips for saving money safely on the cost of prescription drugs.
The antibody service and more efficient processesbostonmol
Boston Molecules contain Antibody services and Base editing which is growing at compound annual rate since 2014 contain biopharmaceutical products which become more dynamic and rapidly expanding in market.
A presentation by J. Aaron Graham, Executive Director of Brand Safety & Security at Boehringer Ingelheim Pharmaceuticals, Inc., about the threat of imported counterfeit prescription drugs.
Crowdsourcing abuse deterrent formulation street price differentials epidemico
This document discusses StreetRx.com, a crowdsourced platform that collects anonymous street price data on diverted pharmaceutical drugs. It has received over 42,000 referrals to health organizations since 2010. The document examines whether abuse-deterrent drug formulations (ADFs) can be distinguished from original formulations based on their street prices. Analysis of over 49,000 price entries found that most ADFs had significantly higher street prices than their non-ADF counterparts, indicating the black market can potentially discriminate between different abuse-deterrent technologies and formulations.
StreetRx collects crowdsourced data on street prices of diverted pharmaceuticals to monitor abuse trends. The document analyzes this data, finding that bulk purchases (10+ units) receive significant discounts compared to individual "retail" purchases for many drug classes, including benzodiazepines, muscle relaxers, erectile dysfunction drugs, and opioids. For example, bulk alprazolam purchases receive a 34% discount on average. This data helps identify which drugs face greater diversion risks due to larger bulk discounts.
Crowdsourcing as a way to evaluate drug abuse in the community epidemico
Can the black market predict which abuse-deterrent formulations are most successful?
Drug companies are trying to make pills harder to crush, in order to deter injection and snorting. The FDA held a public meeting last October where industry experts revealed new secrets on how the products are made, and are putting together a guidance on how to evaluate whether new drugs are really abuse deterrent, and whether pharma companies get to promote that way. Nabarun Dasgupta of Epidemico is presenting today at a new conference of FDA and industry on what black market street prices can reveal about ADFs.
This document is a weekly report from Vypr's COVID-19 Consumer Impact Tracker that measures how consumer behavior is changing in response to the coronavirus pandemic. It tracks 14 metrics related to lifestyle changes, shopping behavior, spending, and attitudes based on surveys of 500 UK consumers. The report shows changes between surveys conducted on March 19th and 25th, with increases seen in people working from home, limiting travel and social interactions, and spending more on groceries and personal care items. Overall it aims to track the evolving impact of the crisis on consumer behavior over time.
The document summarizes statistics about UK consumers' mobile commerce behaviors: 24% of UK consumers have used smartphones to access websites while shopping; 48% accessed retail websites and 50% accessed social media sites on their phones while shopping; 40% of smartphone shoppers ultimately made a purchase in-store, online or via mobile. 55% of UK consumers have seen a QR code while shopping and 33% of those who saw one scanned it. 48% of UK smartphone owners use their phones to research products before purchase.
Cannabis Science & Policy Summit - Day 1 - FortinCannabisSummit
1) The document analyzes cannabis policy and markets in Colorado following legalization of recreational cannabis.
2) It finds evidence that the recreational market is cannibalizing the medical market, especially in tourist counties, but is also expanding overall demand.
3) A dual pricing scheme, with lower prices for medical patients and higher prices for recreational users, has successfully achieved price discrimination and appears optimal for balancing economic and social outcomes.
This document discusses Where Food Comes From, Inc., a company that provides third-party verification and certification services for food producers. It has three main auditing divisions that verify various product attributes and certifications. The document outlines many of the standards, certifications, and attributes that the company can currently verify. It also discusses the importance of third-party verification and traceability in validating claims about food production practices and meeting consumer demand for transparency.
Your CBD business plan has to cover a lot of ground. Regulatory hurdles. Supply chain inconsistency. Marketing restrictions. And even if all those issues are addressed, you still have to create a credible brand in a crowded marketplace.
Fortunately, GemmaCert is here to help. We’ve assembled this guide with valuable information for creating a great CBD business. Because our executive team has extensive experience in the dietary supplement industry — and because CBD is regulated like a dietary supplement in many
jurisdictions — we can help CBD businesses navigate the market.
This document discusses the Partnership for Safe Medicines, an organization advocating for safe medication access. It lists over 100 member organizations and provides information on counterfeit drugs including examples during the COVID-19 pandemic of fake vaccines, testing kits, and medicines being sold. Data is presented on rising drug overdose deaths in the US driven largely by fentanyl, and examples are given of recent seizures of counterfeit pills containing fentanyl in various states and countries that are fueling the opioid crisis.
Prescription Medicines Costs in Context October 2020PhRMA
This document discusses the costs and affordability of prescription medicines in the United States. It notes that while spending on prescription medicines accounts for only 14% of total health care spending, patients face high and rising out-of-pocket costs for medicines. While most medicines sold in the US are generics, brand name medicines face significant price negotiations and rebates paid to insurers and pharmacy benefit managers that often do not lower costs for patients. The document outlines reforms to make medicines more affordable and accessible for patients.
Mobile marketing is gaining popularity in Europe, with 40% of marketers currently using it and 28% planning to start campaigns in the next 12 months. Mobile app adoption among European mobile marketers is 38%, though only 7% of European consumers regularly download apps. Europeans are more likely to browse mobile websites than download apps, and the number of mobile web browsers has doubled in several European countries in the past year. SMS and MMS are popular mobile marketing tactics, used by 40% of mobile marketers.
Prescription Medicines Costs in Context April 2022PhRMA
This document discusses the costs of prescription medicines in the United States. It notes that 60 new medicines were approved by the FDA in 2021 for cancer, hemophilia, and COVID treatments. While brand medicine prices declined slightly in 2020, overall medicine spending grew modestly due to rebates and discounts. The majority of medicine spending goes to entities other than the manufacturers, such as insurers, pharmacy benefit managers, and providers. The document argues for reforms that make insurance work better for patients, modernize Medicare drug coverage, protect safety net programs, and end misaligned incentives in the system.
Purchasing things on mobile is common now and mobile commerce is becoming the part of everyone’s daily routine. Know the global statistics why people are going mobile.
Prescription Medicines Costs in Context March 2022PhRMA
This document discusses trends in prescription drug costs and spending in the United States. It notes that 60 new medicines were approved by the FDA in 2021 for cancer, hemophilia, and COVID. While brand drug prices declined slightly in 2020, overall drug spending grew modestly. Most drug spending goes to health insurers, pharmacy benefit managers, and other entities rather than drug manufacturers. The majority of drugs dispensed are generics, which provide billions in savings each year. The document argues that while drug spending is projected to increase at a similar rate as overall healthcare costs, patients still face high out-of-pocket costs due to deductibles, coinsurance, and other cost-sharing policies by insurers.
Cannabis Science & Policy Summit - Day 1 - MacCounCannabisSummit
This document summarizes key points from Jon's talk on cannabis legalization. It notes that national legalization following an alcohol model is likely. Long-run cannabis consumption may double. Prices and quantity consumed matter more than the number of consumers. There are many policy levers but it is unclear if they are being used effectively to learn what works. National legalization is not guaranteed and effects in states like Colorado are still uncertain due to many complicating factors. The fundamental tradeoff is that legalization may reduce average harm per dose while increasing total doses consumed, with the net public health effect unknown.
Prescription Medicines - Costs in Context - October 2018PhRMA
This document discusses the costs and context of prescription medicines. It notes that while prescription drug spending is a small percentage of total healthcare costs, certain patients face rising out-of-pocket costs. It also outlines the significant costs and risks of developing new medicines, with the average drug taking over 10 years and $2.6 billion to develop. The document proposes reforms to help lower costs for patients while supporting continued research and development of new treatments.
Prescription Medicines Costs in Context November 2019PhRMA
This document discusses the costs and context of prescription medicines. It notes that while prescription drug spending is a small percentage of total healthcare spending, patients often face high out-of-pocket costs. It outlines the significant costs and risks of drug research and development. The document also describes the role of generics in reducing costs over time and how rebates and discounts do not always lower costs for patients.
In this webinar I provide an overview of counterfeits in America, I talk about some myths of importation, and I teach patients and patient advocates some great tips for saving money safely.
This presentation was the main portion of a March 15th, 2012 Congressional briefing in Washington DC on the state of counterfeits in America and the details, as currently known, of the fake Avastin incident.
Tim Mackey, Assistant Professor, University of California, San Diego - Department of Anesthesiology, speaks about the effect counterfeit Avastin has had on efforts to protect the American public from counterfeit medications.
A presentation by J. Aaron Graham, Executive Director of Brand Safety & Security at Boehringer Ingelheim Pharmaceuticals, Inc., about the threat of imported counterfeit prescription drugs.
Crowdsourcing abuse deterrent formulation street price differentials epidemico
This document discusses StreetRx.com, a crowdsourced platform that collects anonymous street price data on diverted pharmaceutical drugs. It has received over 42,000 referrals to health organizations since 2010. The document examines whether abuse-deterrent drug formulations (ADFs) can be distinguished from original formulations based on their street prices. Analysis of over 49,000 price entries found that most ADFs had significantly higher street prices than their non-ADF counterparts, indicating the black market can potentially discriminate between different abuse-deterrent technologies and formulations.
StreetRx collects crowdsourced data on street prices of diverted pharmaceuticals to monitor abuse trends. The document analyzes this data, finding that bulk purchases (10+ units) receive significant discounts compared to individual "retail" purchases for many drug classes, including benzodiazepines, muscle relaxers, erectile dysfunction drugs, and opioids. For example, bulk alprazolam purchases receive a 34% discount on average. This data helps identify which drugs face greater diversion risks due to larger bulk discounts.
Crowdsourcing as a way to evaluate drug abuse in the community epidemico
Can the black market predict which abuse-deterrent formulations are most successful?
Drug companies are trying to make pills harder to crush, in order to deter injection and snorting. The FDA held a public meeting last October where industry experts revealed new secrets on how the products are made, and are putting together a guidance on how to evaluate whether new drugs are really abuse deterrent, and whether pharma companies get to promote that way. Nabarun Dasgupta of Epidemico is presenting today at a new conference of FDA and industry on what black market street prices can reveal about ADFs.
This document is a weekly report from Vypr's COVID-19 Consumer Impact Tracker that measures how consumer behavior is changing in response to the coronavirus pandemic. It tracks 14 metrics related to lifestyle changes, shopping behavior, spending, and attitudes based on surveys of 500 UK consumers. The report shows changes between surveys conducted on March 19th and 25th, with increases seen in people working from home, limiting travel and social interactions, and spending more on groceries and personal care items. Overall it aims to track the evolving impact of the crisis on consumer behavior over time.
The document summarizes statistics about UK consumers' mobile commerce behaviors: 24% of UK consumers have used smartphones to access websites while shopping; 48% accessed retail websites and 50% accessed social media sites on their phones while shopping; 40% of smartphone shoppers ultimately made a purchase in-store, online or via mobile. 55% of UK consumers have seen a QR code while shopping and 33% of those who saw one scanned it. 48% of UK smartphone owners use their phones to research products before purchase.
Cannabis Science & Policy Summit - Day 1 - FortinCannabisSummit
1) The document analyzes cannabis policy and markets in Colorado following legalization of recreational cannabis.
2) It finds evidence that the recreational market is cannibalizing the medical market, especially in tourist counties, but is also expanding overall demand.
3) A dual pricing scheme, with lower prices for medical patients and higher prices for recreational users, has successfully achieved price discrimination and appears optimal for balancing economic and social outcomes.
This document discusses Where Food Comes From, Inc., a company that provides third-party verification and certification services for food producers. It has three main auditing divisions that verify various product attributes and certifications. The document outlines many of the standards, certifications, and attributes that the company can currently verify. It also discusses the importance of third-party verification and traceability in validating claims about food production practices and meeting consumer demand for transparency.
Your CBD business plan has to cover a lot of ground. Regulatory hurdles. Supply chain inconsistency. Marketing restrictions. And even if all those issues are addressed, you still have to create a credible brand in a crowded marketplace.
Fortunately, GemmaCert is here to help. We’ve assembled this guide with valuable information for creating a great CBD business. Because our executive team has extensive experience in the dietary supplement industry — and because CBD is regulated like a dietary supplement in many
jurisdictions — we can help CBD businesses navigate the market.
This document discusses the Partnership for Safe Medicines, an organization advocating for safe medication access. It lists over 100 member organizations and provides information on counterfeit drugs including examples during the COVID-19 pandemic of fake vaccines, testing kits, and medicines being sold. Data is presented on rising drug overdose deaths in the US driven largely by fentanyl, and examples are given of recent seizures of counterfeit pills containing fentanyl in various states and countries that are fueling the opioid crisis.
Prescription Medicines Costs in Context October 2020PhRMA
This document discusses the costs and affordability of prescription medicines in the United States. It notes that while spending on prescription medicines accounts for only 14% of total health care spending, patients face high and rising out-of-pocket costs for medicines. While most medicines sold in the US are generics, brand name medicines face significant price negotiations and rebates paid to insurers and pharmacy benefit managers that often do not lower costs for patients. The document outlines reforms to make medicines more affordable and accessible for patients.
Mobile marketing is gaining popularity in Europe, with 40% of marketers currently using it and 28% planning to start campaigns in the next 12 months. Mobile app adoption among European mobile marketers is 38%, though only 7% of European consumers regularly download apps. Europeans are more likely to browse mobile websites than download apps, and the number of mobile web browsers has doubled in several European countries in the past year. SMS and MMS are popular mobile marketing tactics, used by 40% of mobile marketers.
Prescription Medicines Costs in Context April 2022PhRMA
This document discusses the costs of prescription medicines in the United States. It notes that 60 new medicines were approved by the FDA in 2021 for cancer, hemophilia, and COVID treatments. While brand medicine prices declined slightly in 2020, overall medicine spending grew modestly due to rebates and discounts. The majority of medicine spending goes to entities other than the manufacturers, such as insurers, pharmacy benefit managers, and providers. The document argues for reforms that make insurance work better for patients, modernize Medicare drug coverage, protect safety net programs, and end misaligned incentives in the system.
Purchasing things on mobile is common now and mobile commerce is becoming the part of everyone’s daily routine. Know the global statistics why people are going mobile.
Prescription Medicines Costs in Context March 2022PhRMA
This document discusses trends in prescription drug costs and spending in the United States. It notes that 60 new medicines were approved by the FDA in 2021 for cancer, hemophilia, and COVID. While brand drug prices declined slightly in 2020, overall drug spending grew modestly. Most drug spending goes to health insurers, pharmacy benefit managers, and other entities rather than drug manufacturers. The majority of drugs dispensed are generics, which provide billions in savings each year. The document argues that while drug spending is projected to increase at a similar rate as overall healthcare costs, patients still face high out-of-pocket costs due to deductibles, coinsurance, and other cost-sharing policies by insurers.
Cannabis Science & Policy Summit - Day 1 - MacCounCannabisSummit
This document summarizes key points from Jon's talk on cannabis legalization. It notes that national legalization following an alcohol model is likely. Long-run cannabis consumption may double. Prices and quantity consumed matter more than the number of consumers. There are many policy levers but it is unclear if they are being used effectively to learn what works. National legalization is not guaranteed and effects in states like Colorado are still uncertain due to many complicating factors. The fundamental tradeoff is that legalization may reduce average harm per dose while increasing total doses consumed, with the net public health effect unknown.
Prescription Medicines - Costs in Context - October 2018PhRMA
This document discusses the costs and context of prescription medicines. It notes that while prescription drug spending is a small percentage of total healthcare costs, certain patients face rising out-of-pocket costs. It also outlines the significant costs and risks of developing new medicines, with the average drug taking over 10 years and $2.6 billion to develop. The document proposes reforms to help lower costs for patients while supporting continued research and development of new treatments.
Prescription Medicines Costs in Context November 2019PhRMA
This document discusses the costs and context of prescription medicines. It notes that while prescription drug spending is a small percentage of total healthcare spending, patients often face high out-of-pocket costs. It outlines the significant costs and risks of drug research and development. The document also describes the role of generics in reducing costs over time and how rebates and discounts do not always lower costs for patients.
In this webinar I provide an overview of counterfeits in America, I talk about some myths of importation, and I teach patients and patient advocates some great tips for saving money safely.
This presentation was the main portion of a March 15th, 2012 Congressional briefing in Washington DC on the state of counterfeits in America and the details, as currently known, of the fake Avastin incident.
Tim Mackey, Assistant Professor, University of California, San Diego - Department of Anesthesiology, speaks about the effect counterfeit Avastin has had on efforts to protect the American public from counterfeit medications.
1. Partnership for Safe Medicines China (PSM China) was established in Beijing in November 2012 with participation from 12 associations to ensure a safe drug supply chain and educate patients and consumers on safe medication use.
2. PSM China's members include associations representing pharmaceutical manufacturers, distributors, hospitals, and licensed pharmacists.
3. In 2014, PSM China collaborated with Partnership for Safe Medicines India, launched a website, focused education efforts on medication for the elderly and chronic diseases, and organized over 180 volunteers to support educational programs.
Scott A. LaGanga, Executive Director Partnership for Safe Medicines (PSM) and Senior Vice President, Public Affairs -Advocacy at the Pharmaceutical Research and Manufacturers of America (PhRMA), opens PSM's Interchange 2014.
Daniel Burke, FDA's Senior Special Agent in the Cybercrime Investigations Unit, introduces our 3rd panel at the 2014 Interchange by speaking about how fake online pharmacies can affect American citizens.
Marv Shepherd conducted research exploring whether hospital pharmacies could be a source of diverted drugs. A survey of Texas hospitals found that 25% reported being contacted by "grey market" vendors weekly or daily to purchase pharmaceuticals. Additionally, over 85% of hospitals reported being contacted by such vendors in the last month to sell drugs. While the size of this illicit market is unknown, the findings suggest some hospitals may be unlawfully diverting drugs. Further analysis found no significant associations between vendor contacts and hospital size, ownership, or location. The research indicates opportunistic vendors are actively trying to obtain drugs from some hospitals in Texas.
The document summarizes initiatives to combat counterfeit medicines in various countries. It finds that healthcare professionals' roles are often unclear and they are not always at the forefront of counterfeiting issues. The WHPA campaign aims to strengthen advocacy for investing in healthcare professionals' education and capacity to detect, report, and prevent counterfeits. It establishes dialogue between stakeholders to share knowledge and resources and initiate cost-effective solutions. The WHPA Call to Action and toolkit provide strategies and resources to build comprehensive regional plans against counterfeiting through increasing professional capacity, regional cooperation, collaborative practice, and improved collaboration with authorities.
PSM India aims to: raise awareness of spurious drugs' harm; educate consumers and practitioners on drug quality and identifying suspected spurious drugs; and collaborate with the government and WHO. PSM held an international workshop on ensuring patient safety over commercial interests and regaining consumer confidence. A study found many small manufacturers lack Good Manufacturing Practices compliance and risk producing spurious drugs. It evaluated 348 essential drugs across India to understand the spurious drug problem's full extent and compliance with regulations. PSM plans to expand detection technologies statewide and work with regulators against law-violating manufacturers.
The document summarizes a panel discussion on new developments in international cooperation to address challenges related to unapproved and counterfeit drugs. It describes problems like large quantities of prescription drugs coming from other countries and physicians ordering directly from unlicensed suppliers. Global challenges in investigations like tracing money and packages and obtaining evidence from other countries are also outlined. The panelists discuss international enforcement operations and USP programs that help strengthen quality assurance in developing countries.
Tim Mackey presented on the availability of dangerous, unapproved, and recalled drugs online. Some key points:
- Research has found narrow therapeutic index drugs, drugs not approved for sale, and drugs under global recall are actively being marketed for sale without a prescription online.
- The online drug ecosystem is complex, involving affiliate networks, business-to-business sellers, and emerging technologies like the dark web.
- Moving forward, efforts should identify high-risk dangerous drugs, develop global lists of such drugs, map the entire illicit online pharmacy ecosystem, and prioritize enforcement against the worst offenders. The goal is to improve identification, surveillance and enforcement of clearly dangerous medicines available online without oversight.
The document summarizes the 2013 Interchange conference hosted by the Partnership for Safe Medicines (PSM). It lists the executive director of PSM and its many member organizations. It then describes PSM's efforts over the past year to educate over 300,000 patients, nurses, doctors and pharmacists, and nearly 1,000 at-risk clinics about counterfeit drugs through Facebook ads, printed materials, and trainings. PSM has also been working with international partners in countries like India, China, and Brazil. The conference agenda includes a new panel format and presentations on new research studies.
This document discusses the threats posed by counterfeit medicines. It provides several examples of counterfeit medicines breaching the US supply chain and being distributed through "Canadian" websites and social media sites. The counterfeits have been found to contain no active ingredients, toxic ingredients, or incorrect doses of active ingredients. They are manufactured under unsafe conditions but can appear virtually indistinguishable from real medicines. The document emphasizes that counterfeit medicines pose a real threat to patient health and safety.
The document discusses how American patients have been impacted by unsafe and counterfeit medicines from 2010-2013. It describes several cases where medical professionals purchased non-FDA approved drugs and devices, exposing patients to risks. This includes expired, stolen, or improperly stored medicines. The document outlines issues with specific treatments like IUDs, Botox, osteoporosis drugs, HIV drugs, and diabetes treatments. Patients who received counterfeit versions faced potential health problems. While the full scope of the counterfeit drug problem in the US is unknown, the document argues it threatens patient safety when healthcare providers and patients cannot be certain the treatments they receive are real and effective.
Linda I. Marks, Senior Litigation Counsel, Consumer Protection Branch, U.S. Department of Justice speaks around criminal prosecutions of drug counterfeiters and diverters in the US.
Tom Kubic, President and CEO of the Pharmaceutical Security Institute (PSI) and PSM board member, presents an overview of global activity in the counterfeiting of prescription medicines in 2013.
The UK Medicines and Healthcare products Regulatory Agency (MHRA) has developed a strategy to combat falsified medical products with the objective of reducing risks to patients and consumers. The strategy aims to enhance legal frameworks at the European Union and Council of Europe levels related to falsified medicines and strengthen safety features and controls for actors in the medical supply chain. It also addresses issues like internet sales of medicines and controls on active pharmaceutical ingredients.
This document summarizes a panel discussion on issues related to fake online pharmacies. The panelists included pharmacists, law enforcement agents, and policy experts. They discussed how online pharmacies are difficult to regulate due to their ability to operate across state and international lines. While organizations like the FDA and NABP have programs to verify legitimate online pharmacies, illicit sites still proliferate using search engines, social media, and other online marketing techniques. Research presented found that consumers have difficulty identifying unsafe pharmacy websites and are willing to purchase medicines from illegal online pharmacies without prescriptions, including drugs that require close medical supervision.
Non-FDA approved foreign drugs are being provided to Massachusetts patients through online pharmacies, putting their health at risk. These drugs may contain toxic fillers, expired ingredients, or lack important safety information. Several health groups and trusts in Massachusetts are directing patients to these online pharmacies to reduce costs, incentivizing the purchase of unsafe drugs. Records obtained through FOIA requests show thousands of patients across multiple regions in Massachusetts are affected. Next steps include alerting regulatory agencies to intervene.
The document thanks sponsors for supporting the 2013 Interchange conference. It provides information about materials available to attendees, including a 69-page overview of counterfeit drug policy in the conference packet and educational materials that can be co-branded or used to educate communities. A USB pen is also described that contains graphics, research, and consumer education materials from the Partnership for Safe Medicines.
Fighting black market and counterfeit drugs in America endangers patients. Any break in the regulated, closed supply chain - whether by patients buying drugs online, or medical professionals purchasing from unlicensed distributors - puts lives at risk. Counterfeit or improperly handled treatments for conditions like HIV/AIDS, osteoporosis, kidney disease, and diabetes can be ineffective or even life-threatening when patients' health depends on properly manufactured and stored medicine. Protecting the supply chain is crucial to patient safety.
Online Access to Safe and Affordable Medication: Applying human rights law to...PharmacyChecker
Online Access to Safe and Affordable Medication: Applying human rights law to cyber rule-making and Internet governance
https://www.pharmacychecker.com/
Internet users are benefiting from online access to safe and affordable medications. The pharmaceutical industry views Internet access as a threat and disruptive to its profit model because consumers are paying less than the drug companies intended for them to pay. According to the UN Human Rights Council, access to affordable medication is a human right. As the Internet community seeks to infuse the principles of international human rights law into the discourse and practice of Internet governance it should help maintain the widest possible online access to safe and affordable medication.
https://www.pharmacychecker.com/
The document summarizes key points from a presentation by Daniel Bennett, CEO of Yellow Brand Protection, on anti-counterfeiting efforts in the pharmaceutical industry. It discusses the growth of the global pharmaceutical market and issues around counterfeit and substandard drugs. It also examines the evolution of online pharmaceutical sales channels like webstores, social media, and online marketplaces, noting challenges in regulating these channels, especially in China as it lifts its ban on online drug sales.
The document discusses regulations around online pharmacy services. It notes that while online pharmacies provide convenience, regulatory authorities have concerns about safety due to illegitimate sites that dispense drugs without prescriptions or provide low quality drugs. The document outlines various regulatory approaches taken around the world to address this, including laws, international agreements, accreditation programs, and restrictions on online sales of controlled substances. The goal of regulations is to protect public health by distinguishing between legal and illegal online pharmacies.
The document discusses e-pharmacy, which refers to online platforms for purchasing medicines. It outlines the definition, history, key players, types, components, regulations, and future of e-pharmacy in India. E-pharmacies allow consumers to purchase medicines online without visiting brick-and-mortar stores. While convenient for consumers, e-pharmacy also raises issues around safety, accountability and adherence to pharmacy laws and regulations. The government of India is working to develop policies to regulate e-pharmacies and ensure public health standards are met.
This document discusses the issue of online drug sales via the internet. It notes that prescription drugs can now be easily purchased online, which challenges drug enforcement agencies. The U.S. House held hearings to understand this problem. Some online pharmacies illegally distribute addictive drugs. Trafficking in illegal prescription drugs now equals or exceeds sales of drugs like heroin and cocaine. Online drug sites attract customers with lower prices from countries like Canada and countries in Europe and elsewhere. Efforts are being made to identify and crack down on illegal online pharmacies.
This document discusses the dangers of purchasing prescription drugs from online pharmacies. It provides facts showing that 97% of websites offering to sell medicines online are illegitimate and sell counterfeit drugs. It notes that 23% of adult internet users have purchased prescription drugs online and warns that taking counterfeit medicines can be life-threatening. The document calls for action from internet stakeholders, policymakers, and the public to raise awareness about this issue and disrupt the online sale of counterfeit drugs.
The document provides information on counterfeit drugs, including definitions, global and Indian statistics, examples of counterfeited drugs, and potential solutions. Some key points:
- The WHO defines counterfeit drugs as deliberately mislabeled regarding identity and/or source, and they may contain incorrect ingredients, insufficient active ingredients, or no active ingredients.
- India accounts for 10% of global drug production but also has high rates of counterfeiting, estimated at 20% of drugs. Globally, counterfeiting costs the legitimate pharmaceutical industry $75 billion annually.
- Many popular drugs are frequently counterfeited, such as Viagra, Lipitor, and cancer treatments. Counterfeits are found to contain
The document discusses the benefits and risks of online pharmacies. It outlines the process of online distribution and notes that while e-pharmacies provide convenience, around 96% do not comply with laws. Benefits include lower prices, large selection and 24/7 access, but risks are self-medication without interaction, improper handling of medicines, and sale of controlled substances. Laws prohibit online pharmacies in India without a valid prescription. While e-pharmacies can increase access, proper rules and patient education are needed to ensure safety.
White paper stopping counterfeit pharmaceuticals 0309NEW Momentum
This white paper discusses the growing problem of counterfeit pharmaceuticals and proposes four ways for pharmaceutical companies to address it. It notes that 10% of global drug supply is counterfeit, with some countries over 50%, and counterfeit drug sales are growing much faster than the legitimate market. The paper advocates for counterfeit protection on packaging, RFID tracking in supply chains, security features on dosages, and advanced web monitoring to identify counterfeits. It argues the private sector must lead solutions to protect patients, brands, and industry profits from counterfeiting.
This document discusses counterfeit medicines and measures to combat them. It defines counterfeit medicines according to WHO as those deliberately mislabeled regarding identity and/or source. The most common types of counterfeits are those without active ingredients or with incorrect quantities. Counterfeiting is prevalent in developing countries and online pharmacies. It poses dangers like treatment failure, toxicity, and drug resistance. Detection methods include chemical kits, barcodes, and Raman spectroscopy. Measures to combat counterfeits involve legislation, regulation, international cooperation, and awareness campaigns. Pharmacists play a role in preventing counterfeits from entering the supply chain.
June 19, 2013: This presentation to highlight the dangers of counterfeit drugs to Maine patients was given to the Bangor Dept. of Health Public Advisory committee
Internet marketing involves using websites and online promotional techniques to achieve marketing objectives. It includes using a company website along with search engines, banner ads, and other websites.
The internet can now support the entire marketing process for most businesses. Customers' decision making processes are also significantly impacted by online information. Both patients and doctors now frequently use the internet for health information and research.
Janani Kalyanam - Machine Learning to Detect Illegal Online Sales of Prescrip...MLconf
This document discusses using AI to detect illicit online sales of opioids through social media analysis. It provides background on laws targeting online drug sales without prescriptions. While policy guidelines aim to regulate this, internet effects remain inadequately addressed. The document then presents a pipeline using natural language processing and machine learning to analyze over 1 million tweets, isolate topics related to illicit online pharmacies, and identify characteristics of relevant tweets to build models that can automatically detect emerging bad actors selling drugs online. The goal is to analyze social media content quickly to help address this important problem.
E-Pharmacy
These days buying medicines online has become a common practice all over the world. This is because buyers prefer to order medicines at the click of a button rather than going to a drugstore. Such online websites sell everything from prescription medicines to all health-related products. Most of these stores are legal stores that carry all conventional prescription drugs. Hence most of the buyers are confident about dealing with these stores. But these are just some of the scams that have surfaced on the internet recently. These stores deal in illegal drugs and unapproved drugs. Buyers should be aware of such bullying shops.
The Corona Virus pandemic has significantly impacted consumer shopping behaviour and it is easier than ever to get healthcare products from online retailers, even Amazon.com or a dedicated e-pharmacy, where permitted. attracted more people.
They find convenience, reliability and affordability in every transaction online. They already feel comfortable buying categories like music, food, medicine etc from online retailers and are now looking for similar services for more complex categories like OTC, medical devices and prescription drugs.
The Journey Of Consumer Healthcare Is Shifting To Online Digital Platforms.
Before the spread of coronavirus (covid-19 ), more than 70% of people were researching their health features online, while approximately 49% of consumers were using health products to treat serious conditions. Consumer health monitoring and prescription in parallel with the adoption of technology to treat/manage their health with products, development has created an environment where consumers' healthcare journey is shifting to the online digital platforms.
With the speed of adoption of e-commerce and increase in mobile penetration, shoppers are not limited to self-care shopping. They are also using apps to track health metrics, diagnose themselves and use cloud-based apps to monitor their health in real time.
What corona virus (covid-19 ) has done is accelerate trends that are already on the rise, be it online self-care, telemedicine adoption or online consultation with doctors and pharmacists. The transformation that was expected to take many years is now less than nine months.
How E-Pharmacy Works
E-Pharmacy uploads scanned copies of users' prescriptions and orders the required medicines on the mobile application or website. Registered pharmacists finally analyse and verify the prescription and distribute the medicine accordingly to the users. Availability of medicines, The whole process can take anywhere from a few hours to weeks, depending on the location and supply chain system. Electronic pharmacy is governed by the information technology law of the respective country. These laws cover the privacy of user information, prescription details, and many other relevant provisions.
An important element associated with e-pharmacy is compliance. Companies must be licensed to operate and sell dru
Healthcare providers are increasingly breaking the secure supply chain and endangering patients. Learn about counterfeit drugs and most recent incidents involving providers.
Also learn about how you can be a part of the solution by working with the Partnership for Safe Medicines.
Leveraging Public-Private Partnerships in Surveillance, Enforcement and Preve...Global Risk Forum GRFDavos
Global counterfeit drugs sold online pose a major public health risk. Unregulated internet pharmacies sell counterfeit medicines to unsuspecting consumers around the world, threatening patient safety. Current enforcement efforts are inadequate, as illicit online drug sales can still be easily found. A coordinated, multi-sector approach is needed involving public-private partnerships between law enforcement, regulatory agencies, internet and payment companies, and others. Through active surveillance of online drug sales, information sharing, and prevention efforts, partnerships can help curb this growing global health threat.
Computational approaches using AI are being used to speed up drug discovery and clinical trials in the following ways:
(1) AI is being applied to large datasets to help identify new biomarkers and repurpose existing drugs, with the global AI healthcare market expected to reach $36.1 billion by 2025.
(2) Major pharmaceutical companies are collaborating and sharing data using AI to accelerate target identification and automate molecule design.
(3) Startups are generating huge image datasets from high-throughput drug screening experiments to help identify new drug candidates in areas like oncology.
(4) AI can help improve clinical trials by identifying best patient populations, enabling dynamic trial design adjustments, and improving patient access and
This presentation is designed to train patient advocates in the safety issues around counterfeit drugs: how counterfeits enter our supply chain and how patients can protect themselves.
Similar to PSM Interchange 2014 Panel 3, Libby Baney, The Impact of Fake Online Pharmacies on Patient Safety (20)
PSM presented a special webinar for families affected by counterfeits and fentanyl. Learn about opportunities to make your voice heard. You can watch the presentation at https://youtu.be/FmBv3Bb7ZHI
What have been the major crimes and policy developments in the space of counterfeit medicines? PSM reviews major prosecutions and legislation from the first half of 2021.
This document discusses concerns around safely implementing importation of drugs from Canada. It summarizes perspectives from experts in drug supply chain security and Canadian policy. They note that importation could undermine the Drug Supply Chain Security Act, as drugs from foreign markets don't use the same identifiers and documentation. It may also diminish Canada's drug supply and leave Americans without long-term solutions. The document outlines risks like counterfeiting and how Canadian authorities do not inspect all shipments. It questions whether importation could realistically work given these challenges to safety and oversight.
This document discusses why importing prescription drugs from Canada is not a viable solution to high drug costs in the US. It notes that previous state-level importation programs failed due to lack of savings and inability to adequately regulate foreign pharmacies. Proper testing of imported drugs is very expensive and would consume any savings. There are also safety concerns, as importation would undermine track-and-trace systems and Canada's drug supply is already limited. Law enforcement experts warn that importation could exacerbate the opioid crisis and organized crime may exploit regulatory loopholes. The document argues policymakers should focus on real solutions rather than unrealistic importation proposals.
This document discusses Maine's experience with LD 171, a law passed in 2013 to legalize the importation of prescription drugs from licensed pharmacies in Canada, UK, Australia and New Zealand. It describes how the Maine Pharmacy Association President ordered drugs from an online Canadian pharmacy called Canada Drug Center and found the drugs to be substandard and contaminated. The law was struck down in 2015 because it compromised federal drug regulation. Attempts by other states to import drugs from foreign pharmacies similarly found poor oversight, unsafe drugs, and an inability to regulate foreign entities.
A presentation by Tom T. Kubic, President and CEO, Pharmaceutical Security Institute and Treasurer, Partnership for Safe Medicines about the threat of imported counterfeit prescription drugs.
Marv Shepherd, PSM president, Member USP Package Storage and Distribution Expert Committee, and Professor at the University of Texas at Austin speaks about updates to United States Pharmacopeia's good distribution practices.
The document discusses Maine laws regarding importing prescription drugs from licensed pharmacies in other countries. It states that licensed pharmacies in Canada, UK, Australia, and New Zealand can export prescription drugs by mail to Maine residents for personal use without a Maine license. It also states that entities that facilitate drug exports from these licensed foreign pharmacies to Maine residents are also exempt from needing a Maine license. The document then lists information about specific drugs' manufacturers, fill centers, and mailing addresses.
Gene therapy can be broadly defined as the transfer of genetic material to cure a disease or at least to improve the clinical status of a patient.
One of the basic concepts of gene therapy is to transform viruses into genetic shuttles, which will deliver the gene of interest into the target cells.
Safe methods have been devised to do this, using several viral and non-viral vectors.
In the future, this technique may allow doctors to treat a disorder by inserting a gene into a patient's cells instead of using drugs or surgery.
The biggest hurdle faced by medical research in gene therapy is the availability of effective gene-carrying vectors that meet all of the following criteria:
Protection of transgene or genetic cargo from degradative action of systemic and endonucleases,
Delivery of genetic material to the target site, i.e., either cell cytoplasm or nucleus,
Low potential of triggering unwanted immune responses or genotoxicity,
Economical and feasible availability for patients .
Viruses are naturally evolved vehicles that efficiently transfer their genes into host cells.
Choice of viral vector is dependent on gene transfer efficiency, capacity to carry foreign genes, toxicity, stability, immune responses towards viral antigens and potential viral recombination.
There are a wide variety of vectors used to deliver DNA or oligo nucleotides into mammalian cells, either in vitro or in vivo.
The most common vector system based on retroviruses, adenoviruses, herpes simplex viruses, adeno associated viruses.
- Video recording of this lecture in English language: https://youtu.be/RvdYsTzgQq8
- Video recording of this lecture in Arabic language: https://youtu.be/ECILGWtgZko
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Discover the benefits of homeopathic medicine for irregular periods with our guide on 5 common remedies. Learn how these natural treatments can help regulate menstrual cycles and improve overall menstrual health.
Visit Us: https://drdeepikashomeopathy.com/service/irregular-periods-treatment/
5-hydroxytryptamine or 5-HT or Serotonin is a neurotransmitter that serves a range of roles in the human body. It is sometimes referred to as the happy chemical since it promotes overall well-being and happiness.
It is mostly found in the brain, intestines, and blood platelets.
5-HT is utilised to transport messages between nerve cells, is known to be involved in smooth muscle contraction, and adds to overall well-being and pleasure, among other benefits. 5-HT regulates the body's sleep-wake cycles and internal clock by acting as a precursor to melatonin.
It is hypothesised to regulate hunger, emotions, motor, cognitive, and autonomic processes.
Dr. Tan's Balance Method.pdf (From Academy of Oriental Medicine at Austin)GeorgeKieling1
Home
Organization
Academy of Oriental Medicine at Austin
Academy of Oriental Medicine at Austin
Academy of Oriental Medicine at Austin
About AOMA: The Academy of Oriental Medicine at Austin offers a masters-level graduate program in acupuncture and Oriental medicine, preparing its students for careers as skilled, professional practitioners. AOMA is known for its internationally recognized faculty, award-winning student clinical internship program, and herbal medicine program. Since its founding in 1993, AOMA has grown rapidly in size and reputation, drawing students from around the nation and faculty from around the world. AOMA also conducts more than 20,000 patient visits annually in its student and professional clinics. AOMA collaborates with Western healthcare institutions including the Seton Family of Hospitals, and gives back to the community through partnerships with nonprofit organizations and by providing free and reduced price treatments to people who cannot afford them. The Academy of Oriental Medicine at Austin is located at 2700 West Anderson Lane. AOMA also serves patients and retail customers at its south Austin location, 4701 West Gate Blvd. For more information see www.aoma.edu or call 512-492-303434.
The Children are very vulnerable to get affected with respiratory disease.
In our country, the respiratory Disease conditions are consider as major cause for mortality and Morbidity in Child.
Breast cancer: Post menopausal endocrine therapyDr. Sumit KUMAR
Breast cancer in postmenopausal women with hormone receptor-positive (HR+) status is a common and complex condition that necessitates a multifaceted approach to management. HR+ breast cancer means that the cancer cells grow in response to hormones such as estrogen and progesterone. This subtype is prevalent among postmenopausal women and typically exhibits a more indolent course compared to other forms of breast cancer, which allows for a variety of treatment options.
Diagnosis and Staging
The diagnosis of HR+ breast cancer begins with clinical evaluation, imaging, and biopsy. Imaging modalities such as mammography, ultrasound, and MRI help in assessing the extent of the disease. Histopathological examination and immunohistochemical staining of the biopsy sample confirm the diagnosis and hormone receptor status by identifying the presence of estrogen receptors (ER) and progesterone receptors (PR) on the tumor cells.
Staging involves determining the size of the tumor (T), the involvement of regional lymph nodes (N), and the presence of distant metastasis (M). The American Joint Committee on Cancer (AJCC) staging system is commonly used. Accurate staging is critical as it guides treatment decisions.
Treatment Options
Endocrine Therapy
Endocrine therapy is the cornerstone of treatment for HR+ breast cancer in postmenopausal women. The primary goal is to reduce the levels of estrogen or block its effects on cancer cells. Commonly used agents include:
Selective Estrogen Receptor Modulators (SERMs): Tamoxifen is a SERM that binds to estrogen receptors, blocking estrogen from stimulating breast cancer cells. It is effective but may have side effects such as increased risk of endometrial cancer and thromboembolic events.
Aromatase Inhibitors (AIs): These drugs, including anastrozole, letrozole, and exemestane, lower estrogen levels by inhibiting the aromatase enzyme, which converts androgens to estrogen in peripheral tissues. AIs are generally preferred in postmenopausal women due to their efficacy and safety profile compared to tamoxifen.
Selective Estrogen Receptor Downregulators (SERDs): Fulvestrant is a SERD that degrades estrogen receptors and is used in cases where resistance to other endocrine therapies develops.
Combination Therapies
Combining endocrine therapy with other treatments enhances efficacy. Examples include:
Endocrine Therapy with CDK4/6 Inhibitors: Palbociclib, ribociclib, and abemaciclib are CDK4/6 inhibitors that, when combined with endocrine therapy, significantly improve progression-free survival in advanced HR+ breast cancer.
Endocrine Therapy with mTOR Inhibitors: Everolimus, an mTOR inhibitor, can be added to endocrine therapy for patients who have developed resistance to aromatase inhibitors.
Chemotherapy
Chemotherapy is generally reserved for patients with high-risk features, such as large tumor size, high-grade histology, or extensive lymph node involvement. Regimens often include anthracyclines and taxanes.
PSM Interchange 2014 Panel 3, Libby Baney, The Impact of Fake Online Pharmacies on Patient Safety
1. The Impact of Fake
Online Pharmacies on
Patient Safety
Libby Baney, J.D., Executive Director, ASOP
Partnership for Safe Medicines Interchange
September 18, 2014
2.
3. What We Know: Data
• 40,000-50,000 active online drug sellers
operating globally (LegitScript)
• 97% of online drug seller sites are operating
in violation of applicable laws (NABP)
• 50% of the prescription medicines sold online
by websites that hide their physical address
are counterfeit (WHO)
4. What We Know: Data
Illegal online drug sellers are the most frequent
conduit of counterfeit drugs (NABP)
23% of adult Internet consumers surveyed
have bought prescription medicine online (US
FDA)
Illegal online drug sellers can make $1 million
and $2.5 million in sales each month (MIT)
5. Risks to Patient Safety:
Illegal online drug sellers:
1. Sell prescription-only medicines
without a valid prescription.
2. Sell unapproved, adulterated,
misbranded or counterfeit drugs
3. Do not have the required
pharmacy license in
the jurisdictions it ships drugs to.
7. Examples of Patients Harmed
Lorna Lambden
No medical exam; bought unapproved sleeping pills
Died from drug interaction
Marcia Bergeron
Fake drugs bought from illicit online pharmacy
Heavy metal poisoning (lead, titanium, arsenic)
Steven Kovacs
Bought prescription drugs online without a prescription
Overdosed and died / no medical supervision
10. Five Signs We Are Making An Impact
1. Internet commerce companies agree to take voluntary
action against illegal online drug sellers
• Visa issues Internet Pharmacy Guide for Acquirers
• CSIP issues Principles of Participation
• Realtime Register B.V. (Netherlands) changes practices
Top 10 Registrars Harboring Rogue Pharmacies
1. TodayNIC (China)
2. BizCN (China)
3. Gransy (Czech Republic)
4. Joker.com (Germany)
5. Momentous Group/Rebel.com (Canada)
6. Paknic (Pakistan)
7. WebNIC.cc (Malaysia)
8. Dattatec (Argentina)
9. IPMirror (Singapore)
10. Domain.com (US)
11. Five Signs We Are Making An Impact
2. Transatlantic IPR Working Group prioritizes Internet
pharmacies
3. APEC creates an Internet Sales Working Group
• ASOP helps lead engagement with 21 economies
12. Five Signs We Are Making an Impact
4. DotPharmacy launches (Fall 2014)
5. ASOP raises public awareness
• ASOP issuing a CME/CPE program with the Federation of State
Medical Boards
• ASOP and CSIP run a search advertising campaign:
5.5+ million hits to date
• ASOP speaks at 20+ events annually
13. ASOP is a nonprofit organization with the mission to protect patient safety globally
Federation of State Medical
Boards
National Health Council
National Association of
Boards of Pharmacy
PhRMA
Partnership for Safe
Medicines
Rx-360
APhA
LegitScript
Amgen
Merck
Boehringer Ingelheim
Men’s Health Network
Consumer Healthcare
Information Corp
NACDS
Eli Lilly & Company
NeedyMeds
ASOP Observers
MEMBERS
EAASM
NOVA ScriptCentral
GPhA
Takeda
International Pharmaceutical
Federation
Italian Medicines Agency
Partnership for Drug-Free
Kids
U.S. Pharmacopeia
Convention