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DNA sequencer manufacturer Illumina has also invested $20 million in the project, which builds on a 2021 investment and partnership from Microsoft, which will provide the cloud infrastructure for the project. Pharmaceutical company Regeneron has invested $119.5 Continue to STAT+ to read the full story…
Between 2017 and 2021, regulators in the U.S. Of 104 reports of supply chain issues with dozens of drugs, meaningful shortages were 40% less likely to occur in Canada than in the U.S., a new study found, and the difference was largely attributed to the approach taken by the Canadian government to the problem.
After the world’s largely disastrous response to the coronavirus, countries tasked the WHO with overseeing a pandemic treaty in 2021; negotiations concluded early Wednesday on an agreement expected to be adopted next month at the U.N. health agency’s annual meeting in Geneva. Read the rest…
In 2021, the company spun out Isomorphic Labs, an AI drug discovery company. The Alphabet-owned AI company took the biology world by storm in 2020 with AlphaFold2 , the protein structure prediction AI platform that “solved” a decades-old biology problem.
Medicare Advantage insurers pulled in an estimated $33 billion in additional payment from the government in 2021 as a result of these extra diagnoses, or codes, that made their members seem sicker, relative to people in the traditional Medicare program.
Analysis includes innovative medicines with approved indications or indication extensions that were reimbursed since 2021. On average, 58% of branded drugs approved between 2021 and 2024 in Europe have either fully or restricted reimbursement. Patient profiles were counted distinctly.
In 2021, for instance, 59% of companies scored highly, compared with 41% in 2018. The back-to-back declines come after 60% of patient groups believed the industry fared well thanks to the initial response of many companies to quickly develop salves for the Covid-19 pandemic. Continue to STAT+ to read the full story…
billion from 2021 to 2025 YTD, with ASOs contributing over half ($3.54 Large pharmaceutical companies like AbbVie, Eli Lilly, Roche, and Takeda have shown significant interest, representing 63 per cent of licensing deals from 2021 to 2025 YTD. billion) and siRNAs accounting for more than a third ($2.51
The National Commission for Allied and Healthcare Professions Act, introduced in 2021, standardises education and practice for AHPs, a crucial step in addressing the skill gap exposed by the pandemic. For example, the Skill India Mission 2.0
Recommendations for cancer treatments were reviewed through December 2021. The analysis tallied a total of 258 approved drugs for which companies submitted applications between 2009 and 2020, and then examined funding recommendations that were subsequently made through December 2020 for most drugs.
” FDA.gov, 2021. ” AccessibleMeds.org, 2021. Janet Woodcock, Director of the FDA’s Center for Drug Evaluation and Research Sources cited: U.S. Food and Drug Administration. “Generic Drugs: Questions & Answers.” Association for Accessible Medicines. Kesselheim, A.S., ” JAMA, 2016.
It closed Friday valued at a hair under $50 million, a calamitous fall from 2021, when it went public and soared to a nearly $6 billion market cap. The company will now try to sell itself through a court-supervised sale. In a statement released on Linkedin, Wojcicki made clear she plans to continue attempting to purchase 23andMe.
NHS England will relaunch ‘improved’ anti-smoking pill varenicline after withdrawal of a branded version in 2021. Varenicline, previously available as Champix, will be offered by pharmacy and council-led stop smoking services in England and is expected to help over 85,000 people try to stop smoking each year.
Jana Miller owned a company that provided home health and other services to people with developmental disabilities, but in early 2021, she was found to have engaged in fraudulent billing. Continue to STAT+ to read the full story…
2021, May 2). Key Pillar of a Successful CDMO: Exceptional Regulatory Compliance. Societal CDMO. link] UPM Pharmaceuticals. IND, NDA & ANDA Challenges and How a CDMO Can Help. UPM Pharmaceuticals. link] LGM Pharma. Why A CDMO Might Be The Best Place To Find Regulatory Support. LGM Pharma. link] Pharmaceutical Technology. 2023, June 23).
And, as you can see from FDAs 2025 CDER Guidance Agenda , DPD was working on guidance documents from 180-day generic drug exclusivity, 3-year exclusivity, 30-month stays, pediatric exclusivity, comparative analyses for drug-device combination products, and many other guidance documents on generic drug sameness (including, we understand, a revised version (..)
Drug companies notified the Department of Health and Social Care (DHSC) about disruptions to supply 1,938 times during last year the highest number since the 1,967 seen in 2021. Continue reading.
The European Pharmacopoeia included rFC testing in 2021 through chapter 2632, though rCR technology still requires validation. Regulatory framework evolution The regulatory landscape demonstrates varying degrees of acceptance for recombinant technologies across major pharmacopoeias.
2021 Aug 1;94:103086. I am happy to help how I can. References Reuter P, Pardo B, Taylor J. Imagining a fentanyl future: Some consequences of synthetic opioids replacing heroin. International Journal of Drug Policy. PMID 33423915 Pesce A, Bevins N, Tran K, Thomas R, Jensen K. Changing Landscape of Fentanyl/Heroin Use and Distribution.
The analysis was based on national prescription records for more than two million Danish women between 1996 and 2021. Some hormonal contraceptives are associated with a small but significant increased risk of stroke and heart attack, according to a large and detailed study from Denmark.
86, 72703 (December 22, 2021), DEA emphasized in the Gulf Med decision that prescribing [r]ed flags are circumstances surrounding a prescription that cause a pharmacist to take pause, including signs of diversion or the potential for patient harm. As mentioned in Federal Register Vol.
Lancet 2021; 398(10295): 143-155. Efficacy and Safety of Once Weekly Tirzepatide, a Dual GIP/GLP-1 Receptor Agonist Versus Placebo as Monotherapy in People with Type 2 Diabetes (SURPASS-1). Abstract 100-OR. Presented virtually at the American Diabetes Association’s 81st Scientific Sessions; June 25-29. Rosenstock, J, et. Hypertension.
As part of this, we have committed to reducing absolute Scope 1 and 2 GHG emissions by 42 per cent by the end of 2030 (2021 base year) and to set a supplier engagement target for Scope 3 emissions. The post Strengthening our presence within APAC through increased penetration is a key focus appeared first on Express Pharma.
According to a 2021 study by the Tufts Center for the Study of Drug Development, the average cost to develop a new drug is a staggering $2.6 Sources cited: Tufts Center for the Study of Drug Development, 2021 World Intellectual Property Organization (WIPO), 2019 Source billion[1].
based Bionique Testing Laboratories (2021), and biologics CDMO Bionova Scientific (2022). The division also incorporates international subsidiaries and acquisitionsAustria-based virus safety testing provider ViruSure (acquired in 2019), U.S.-based
Zai Lab obtained exclusive rights in January 2021 to develop and commercialise efgartigimod in Greater China* from argenx. As a once-weekly subcutaneous injection, it addresses unmet needs, surpassing traditional options like corticosteroids and IVIg. Vyvgart is already approved in the US for generalised myasthenia gravis (gMG) and CIDP.
The RPS will deliver the NHS England Foundation Trainee Pharmacist Programme e-Portfolio for another year after NHS England extended the contract, which began in 2021. Pharmacist trainees can continue to access the e-Portfolio for foundation-year as the Royal Pharmaceutical Society (RPS) has been awarded a contract extension.
Ahmed and Mohamed Sirajudeen and Suhaib Chaudhry used testing labs in Illinois and Texas to submit nearly $900 million in fraudulent claims to the federal government between April 2021 and June 2022.
The retrospective cohort study included all patients who met the criteria for the Medicare HRRP COPD model discharged between May 2021 and August 2023. The researchers included 187 patients and 92 patients in the pre- and postimplementation groups, respectively.
Dr Pai succeeds Dr Sanish Davis, who served as President from 2021 to 2025. The Indian Society for Clinical Research (ISCR) has announced the appointment of Dr Seema Pai as President for the 20252028 term. The new leadership team also includes Anirban Roychowdhury as Honorary General Secretary and Amita Bhave as Treasurer.
Updated May 17, 2021. Hikma receives FDA approval for TYZAVANTM (Vancomycin Injection, USP) in the US. News release. July 2, 2025. Accessed July 2, 2025. Cleveland Clinic. Septicemia. News release. Accessed July 2, 2025. Cleveland Clinic. Endocarditis. News release. Updated May 12, 2025. Accessed July 2, 2025.
1 “Based on the totality of evidence regarding cardiovascular benefits of GLP-1 receptor agonists, the 2021 American Heart Association stroke guidelines remain valid for antidiabetic therapy in patients with T2D and stroke,” Inzucchi concluded. The most recent meta-analysis showed a stroke treatment effect estimate of 0.86
billion in 2021 to $17.0 Wong concludes, Although implementation of LAIs as the standard of care is low due to their considerably higher ACOT and patient and/or physician preference for oral antipsychotics, LAI sales accounted for over half of the total atypical antipsychotic sales in 2021. per cent from $8.4
The company ranks as the second fastest-growing firm among the top 30 in terms of domestic sales between MAT December 2021 and MAT December 2024. The appointments come as CORONA Remedies continues to grow within the Indian Pharmaceutical Market (IPM).
Pharmacy Focus Episode 14: The Neurological Impact of COVID-19 Pharmacy Focus Episode 15: Community Pharmacists and COVID-19 Testing Pharmacy Focus Episode 16: Coronasomnia: The Unspoken Adverse Effect of the Pandemic Pharmacy Focus Episode 17: Keeping Up with the COVID-19 Vaccine Pharmacy Focus Episode 18: Performance Measures and Leadership in Pharmacy (..)
Standards of medical care in diabetes – 2021. Impact of a culturally tailored diabetes education and empowerment program in a Mexican American population along the US/Mexico border: a pragmatic study. J Clin Med Res. 2020;12(8):517-529. doi:10.14740/jocmr4273 American Diabetes Association. Clin Diabetes. 2021;39(1):14-43.
2021, November 2). [link] Lawless, L. 2016, November 11). Overcoming Challenges in the Emerging Biosimilar Landscape. National Association of Managed Care Physicians. link] Kurki, P., Interchangeability of Biosimilars: Overcoming the Final Hurdles. National Center for Biotechnology Information. link] Algorics. 2023, June 13).
The company also markets its bevacizumab biosimilar under the name ABEVMY in Europe (approved February 2021) and Canada (approved November 2021). Shreehas Tambe, CEO & Managing Director of Biocon Biologics, said, The U.S. and a strong addition to our robust oncology portfolio.
11 National Health Council, Policy Recommendations for Reducing Health Care Costs , September 2021, [link] costs/#:~:text=The%20NHC%20strongly%20opposes%20policies,as%20defined%20by%20the%20patie nt. 15 Inflation Reduction Act of 2022 , Pub.
Isabelle joined Roquette as Chief Financial Officer in 2021, also overseeing Digital, M&A and Strategy. Since joining the company in 2021 as Head of Business Finance, Batrice has played a pivotal role in shaping Roquette’s business finance strategy and operations.
It was originally approved in 2021 for the treatment of polycythemia vera and the manufacturer, as of January 2025, is seeking to expand the agent’s indication to the treatment of essential thrombocytopenia based on data from the SURPASS-ET trial (NCT04285086). November 12, 2021. Pharmacy Times. June 3, 2025. Accessed June 30, 2025.
We have committed to reduce our scope 1 and 2 GHG emissions by 42 per cent (absolute) by the end of 2030 (from a 2021 basis). As a first step toward this ambition, Lonza has set Near-Term GHG emissions reduction targets that have been validated by the Science-Based Targets initiative (SBTi).
Wegovy was first approved in the US in 2021 and reached the UK market in early 2023. Wegovy was released even earlier than Mounjaro, receiving approval in the US in 2021. In clinical trials, Wegovy helped patients lose up to 15% of their body weight. It became widely available in the UK in 2023.
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