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India has long been recognized as a significant player in the global pharmaceutical industry, particularly in the production of generic drugs. The country’s pharmaceutical sector has experienced substantial growth over the years, driven by both domestic and international demand for affordable and high-quality medicines.
London, 25/10/2023: The pharmaceutical industry is currently responsible for over four per cent of global carbon emissions and this figure is on track to grow in the coming years. Here Simon Farnfield, event director at Lab Innovations, discusses the changes that are allowing the pharmaceutical industry to go green at last.
By increasing access to affordable medications, biosimilars can also help to reduce healthcare costs for employers, insurers, and governments. This will not only benefit patients but also help to drive innovation in the pharmaceutical industry. But the benefits of biosimilars extend far beyond individual patients.
In the vast realm of pharmaceutical research and development, there’s a fascinating intersection between ancient wisdom and modern science. “Pharmacognosy is the bridge between traditional medicine and modern pharmaceutical science, offering a treasure trove of potential new drugs waiting to be discovered.”
Deal Structuring Deal structuring in pharmaceutical M&A requires a balance of financial, legal, and strategic considerations. Intellectual Property Valuation Valuing intellectual property (IP) assets is a critical component of pharmaceutical M&A, as these assets often represent a significant portion of a company's value.
Karst — If you monitor Regulations.gov dockets and litigation dockets on PACER like we do, then you know that one company name—more than any other over the past several years—pops up: Vanda Pharmaceuticals, Inc. VANDA PHARMACEUTICALS, INC. VANDA PHARMACEUTICALS, INC. 24-270 VANDA PHARMACEUTICALS, INC. 23-5200 (D.C.
The stakes for AI adoption in the pharmaceutical industry have never been higher. Yet, the critical question remains: How can pharmaceutical companies ensure responsible and compliant AI implementation while maximizing its potential for field teams?
Medicaid and Government Pricing Congress. The Medicaid and Government Pricing Congress , an important event dedicated to critical policy updates and approaches to effectively contract, report and comply with state and federal healthcare programs, returns June 8-11, 2021. More Interaction.
HP&M) seeks to add an experienced attorney (7+ years) to our government discount program and price reporting practice. Hyman, Phelps & McNamara, P.C. (HP&M) Our firm culture is collaborative, and the subject matter is intellectually stimulating. Strong verbal and writing skills are required.
Medicaid and Government Pricing Congress. The Medicaid and Government Pricing Congress , an important event dedicated to critical policy updates and approaches to effectively contract, report and comply with state and federal healthcare programs, returns June 8-11, 2021. More Interaction.
Government initiatives: Both countries have implemented policies to address patent thicket issues and promote innovation. Compulsory licensing: India has used compulsory licensing to address patent thicket issues in critical areas like pharmaceuticals.
A joint letter co-signed by the Royal Pharmaceutical Society, the British Medical Association, the Royal College of GPs, patient group National Voices and others has called for the UK government to change the law regarding pharmacists’ powers to alter prescriptions.
government and other private-sector companies such as Moderna to support in the distribution of COVID-19 vaccines and the ancillary supply kits. government.
McKesson has a long history of managing the pharmaceutical and medical supply chain in the U.S., A worker at McKesson’s Olive Branch, Miss.
The U.S.
Come together with leaders from the pharmaceutical, biotechnology, and diagnostic industries to unpack huge changes at the American Conference Institutes 23rd Advanced Summit on Life Sciences Patents , which is scheduled to take place from May 19-20, 2025 at the New York Bar Association in New York, NY.
The US Government recently modified their policy to utilize tariffs to in an effort to support the US economy. Pharmaceutical tariffs of 25% have been forecasted causing many global organizations to investigate the consequences of the tariffs on their overall product portfolio.
The British government has contacted medicine suppliers urging them to stockpile drugs for a possible no-deal Brexit, despite the pressure the coronavirus pandemic has had on their current stockpiles. The government wants to sure up supplies for the general population as well as the National Health Service. Photo by Rennett Stowe.
Johnson & Johnson Announces Agreement in Principle with Government of Canada to Supply its COVID-19 Vaccine Candidate. Johnson & Johnson Announces Agreement in Principle with Government of Canada to Supply its COVID-19 Vaccine Candidate. MONTRÉAL, QC – August 31, 2020 – Janssen Inc., Source link.
– Victorian State Government extends financing of JJIPO@Monash for an additional two years. Johnson & Johnson Innovation announced today the extension of the Johnson & Johnson Innovation Partnering Office at Monash University’s Clayton Campus in Melbourne (JJIPO@Monash) in collaboration with the Victorian State Government.
The UK Government has signed a new deal with Johnson & Johnson and Novavax to secure 90 million orders of their vaccine candidates to protect against COVID-19 infection. . S, the COVID-19 vaccine candidate developed by Janssen, the pharmaceutical subsidiary of J&J, for not-for-profit emergency pandemic use.
Government for 100 Million Doses of Investigational COVID-19 Vaccine. Government for 100 Million Doses of Investigational COVID-19 Vaccine. August 05, 2020 – Johnson & Johnson (NYSE: JNJ) (the Company) today announced its Janssen Pharmaceutical Companies have entered into an agreement with the U.S. New Brunswick, N.J.,
Formulation chemistry is the systematic and step-by-step approach to pharmaceutical development. Nowadays, as the usage of medicines is increasing, pharmaceutical companies are more eager to bring manufacturing a new look in quality and performance. There are different tests to assess the quality of a pharmaceutical product.
Environmental Impacts of Traditional Pharmaceutical Production Traditional pharmaceutical manufacturing is complex, with each phase contributing to environmental degradation. The extraction and synthesis of active pharmaceutical ingredients (API) utilize vast amounts of water and energy.
Note that the forecasts below did not account for policy changes that could further reduce pharmaceuticals' share of U.S. Thus, the government actuaries expect that pharmaceuticals will not be the key driver of U.S. healthcare spending. Click here to see the original post from April 2022. spending on healthcare.
Federal Court Orders Puerto Rico Pharmaceutical Distributor to Pay $12 Million in Connection with Alleged Failure to Report Suspicious Orders of Pharmaceutical Drugs and Other Controlled Substance Violations, Nov. The government asserted additional allegations that are outside our scope. 6, 2023 ( DOJ Press Release ).
Thus, the government actuaries expect that pharmaceuticals will not be the key driver of U.S. What’s more, taxpayers—via Medicare and Medicaid—will continue to crowd out the private insurance market. One bright spot: consumers will account for an ever-smaller share of drug spending. healthcare spending growth. to 1:30 p.m.
We intend to bring together people from the entire drug channel: pharmaceutical manufacturers, pharmacy benefit managers (PBMs), health plans, insurers, and plan sponsors, wholesalers and distributors, pharmacies, providers, buying groups, government officials, and more.
As the pharmaceutical industry is pushing to deliver new and better drugs while racing against time and budget constraints, it is becoming crucial to not just use artificial intelligence (AI) but truly maximize its potential. Invest in Your Tech Infrastructure A solid tech foundation is essential for AI to work in the pharmaceutical sector.
Hal came to the pharmaceutical business at mid-career, age 39. After his government work, Hal seized an opportunity to help build a new, not-for-profit organization, Family Planning International Assistance (FPIA), in New York City. This work took him to some 50 countries and allowed Hal to meet pharmaceutical business leaders.
We also summarize the key information pharmaceutical companies and contract research organizations (CROs) need to know to prepare for compliance. This article explores the likely impact of the AI Act on software and systems used in clinical research and how it affects entities outside the EU.
5, 2020 /PRNewswire/ — Johnson & Johnson (NYSE: JNJ) (the Company) today announced its Janssen Pharmaceutical Companies have entered into an agreement with the U.S. government for the large scale domestic manufacturing and delivery in the U.S. government may also purchase an additional 200 million doses of Ad26.COV2.S
Over the years, Advarra has reviewed a wide range of clinical research studies and worked every day alongside leading pharmaceutical manufacturers, medical researchers, and healthcare institutions. Advarra draws members from leading academic institutions, government agencies, and clinical research organizations.
A new shift is occurring in the pharmaceutical industry, leading to a rapidly expanding field known as digital therapeutics (DTx). DTx interventions include sensor-equipped wearable devices, remote patient monitoring tools, and virtual reality platforms integrated with conventional pharmaceutical treatments.
Featured Faculty Driving the Conversation: Rosalind Davis, Government Pricing & Contracts Director , Vifor Pharma, Inc. Attendees of Commercial Contracts & Chargebacks 2023 have the option to add a third day of content to their schedule and join the Medicaid & Government Pricing Congress attendees for their final day.
The US Government recently modified their policy to utilize tariffs to in an effort to support the US economy. Pharmaceutical tariffs have been announced causing many global organizations to investigate the consequences of the tariffs on their overall product portfolio.
Our joint goal is to bring innovation to cancer patients by building a robust, sustainable pipeline in oncology,” said Dominik Ruettinger, Global Head of Research and Early Development for Oncology, Pharmaceuticals Division, Bayer AG. The research is guided by joint project and governance teams.
President and CEO, National Pharmaceutical Council Julie Ritchie Wagner, Senior Assistant General Counsel, Head of Global Ethics, Compliance, and Enforcement Legal Policy, PhRMA Joel White, Founder and President, Horizon Government Affairs Charlene Keller Fullmer, Assistant U.S. O’Brien, Pharm.
The stakes for AI adoption in the pharmaceutical industry have never been higher. Yet, the critical question remains: How can pharmaceutical companies ensure responsible and compliant AI implementation while maximizing its potential for field teams?
What regulatory division governs ICPs? As the prevalence of respiratory diseases continues to rise, the development of ICPs plays a pivotal role in addressing both clinical and patient-centered needs. However, these products present unique challenges from a Chemistry, Manufacturing, and Controls (CMC) standpoint.
You'll return to the office having mastered complex regulatory guidelines to deliver compliant government pricing and reporting programs. Don’t miss the Medicaid Drug Rebate Program Summit coming up this fall in Chicago (or virtually). And so much more !
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The pharmaceutical landscape is evolving rapidly, with small and medium-sized biotech companies increasingly taking center stage in innovation. Managing Quality and Compliance Quality and regulatory compliance are non-negotiable in pharmaceutical manufacturing. How can you ensure your CDMO is up to scratch?
Good laboratory practice (GLP) ensures the safety, quality, and organization of pharmaceutical research. The practice is followed to maintain consistently high standards and comply with any regulations set by government agencies, internal company procedures, and international regulations, like the 3Rs.
Second, governments in high-income foreign countries engage in some form of bargaining with drug companies on drug prices. the EU, and other high-income countries with the most stringent pharmaceutical and pharmacy standards. The theory covers four “stylized facts” of the international market in prescription drugs.
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