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for 2018 and 2020. In what one U.S. lawmaker described as possibly the “largest tax-dodging scheme” by a pharmaceutical company in history, Pfizer sold $20 billion in medicines to U.S. customers, but treating the profits as foreign income for tax purposes.
In May 2024, the Massachusetts Department of Public Health released a troubling report on a cluster of HIV infections, with more than 200 new cases since 2018 attributable to injection drug use in the Boston region.
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…
References [link] [link] per cent20S per cent26amp per cent3BT_Incubator_ %2016–5-2018.pdf pdf [link] [link] [link] [link] [link] [link] The post Incubators and innovation hubs: Accelerating entrepreneurship in life sciences appeared first on Express Pharma.
Hyderabad’s Pharma City, which has been under construction since 2018, is a significant example of this initiative. These parks are critical in reducing India’s reliance on China and making the country an attractive location for pharmaceutical manufacturing.
Making Prescription Drugs Affordable. Retrieved from [link] National Academies of Sciences, Engineering, and Medicine. Making Medicines Affordable: A National Imperative. Retrieved from [link] National Academies of Sciences, Engineering, and Medicine. Retrieved from [link] Source
References Operating losses at the Ebitda level, where Ebitda is earnings before interest, taxes, depreciation and amortisation Wellness products refer to various health, dietary and fitness supplements The Ministry of Health and Family Welfare published draft Rules on 28th August 2018 to amend the Drugs and Cosmetics Rules, 1945, aiming to regulate (..)
2018, March 29). Lean & Operational Excellence in Life Science CDMO’s. Retrieved from [link] GBI Bio. 2024, February 29). Overcoming Scalability in Biologics: CDMO Strategies for Success. Retrieved from [link] Pharmasalmanac. Transforming A CDMO Using an Operational Excellence Approach. Retrieved from [link] Source
Collaboration with HWB In the year 2018, the Heavy Water Board recognised the potential of non-nuclear applications and took the first step in collaborating with two Indian Private organisations to encourage the development and manufacturing of deuterated products.
The regulatory confidence becomes evident when considering that pharmaceutical products tested using rFC have received approval since 2018, demonstrating practical acceptance of recombinant methods. USP Chapter 86, now official, describes alternative methods alongside traditional LAL testing in Chapter 85, treating both rFC and rCR equally.
When the General Data Protection Regulation (GDPR) 1 came into effect in 2018, this appeared to accelerate the migration out of Europe for pharmaceutical clinical trials. This was not so much due to non-compliance but stemmed from regulatory ambiguity.
2009 Clopidogrel Therapy and CYP2C19 Genotype, 2018 EMA recommendations on DPD testing prior to treatment with fluorouracil, capecitabine, tegafur and flucytosine, 2020 Tramadol Therapy and CYP2D6 Genotype, 2021
Milken Institute; 2018. 2022;327(6):534-545. doi:10.1001/jama.2022.0078 2022.0078 Metabolic non-communicable disease health report of India: the ICMR-INDIAB national cross-sectional study (ICMR-INDIAB-17) – The Lancet Diabetes & Endocrinology Waters H, Graf M. Americas Obesity Crisis: The Health and Economic Costs of Excess Weight.
External Links Guide to Good Dispensing Practice, 2016 Expanding the Universal Medication Schedule: a patient-centred approach, 2014 A Patient-Centered Prescription Drug Label to Promote Appropriate Medication Use and Adherence, 2016 Safer dispensing labels for prescription medicines, 2018 National Standard for Labelling Dispensed Medicines, 2021 MOH (..)
The Academy of Digital Health Sciences, founded in 2018, provides digital health courses for doctors, nurses, pharmacists, and healthcare professionals. The post DCGI launches Professional Development Programme in digital health for pharmacists appeared first on Express Pharma.
NaMuscla, which has been designated orphan drug status, received EU marketing authorisation in December 2018. NaMusclareduces myotonia symptoms in people with NDM, resulting in a significant improvement in quality of life and other functional and clinical outcomes for patients.
Dr Saxena joins an eminent group of Indians who have received the Order of Friendship , including chess grandmaster Viswanathan Anand (2018), former Member of Parliament Murli Manohar Joshi, scientist Dr A.S. This recognition fuels our commitment to innovation and cross-cultural solidarity.
It has received several certifications, including ISO 9001:2015, ISO 14001:2015, and ISO 22000:2018. The promoters, Harshad Nanubhai Rathod, Vivek Ashok Kumar Patel, Mayur Popatlal Sojitra, and Hardik Mukundbhai Prajapati, established Accretion Pharmaceuticals in 2012. The company has registered 35.66 crore in the fiscal year 2024.
The [surrogate endpoints report] was developed following the challenges arising from changes in pharmaceutical clinical trials and regulation” They highlighted that products given conditional or accelerated approval by the European Medicines Agency (EMA) between 2011 and 2018 have predominantly relied on non-validated surrogate endpoints this (..)
December 13, 2018. American Oncology Network. August 8, 2024. Accessed May 15, 2025. How your oncology peers manage the complexities of care. Oncology Live ®. Accessed May 15, 2025. Desimone R. Improve work performance with a focus on employee development. December 12, 2019. Updated January 19, 2024. Accessed May 15, 2025.
TYVYT(sintilimab injection), is one of the top therapy choices in immunotherapy, and has already benefited millions of cancer patients since its launch in 2018. Under the agreement, Mankind Pharma will have exclusive rights to register, import, market, sell and distribute sintilimab in India.
December 2018. link] articles/2018/12/dysmenorrhea-and-endometriosis-in-the-adolescent 4. American Pharmaceutical Association; 2025. Dysmenorrhea and endometriosis in the adolescent. American College of Obstetricians and Gynecologists. Accessed April 28, 2025. Smith RP, Kaunitz AM. UpToDate.
12 (December 2022), [link] 3 National Academies of Sciences, Engineering, and Medicine, Health-Care Utilization as a Proxy in Disability Determination (Washington, DC: National Academies Press, March 1, 2018), chap. Finkelstein et al., 2, Factors That Affect Health-Care Utilization, https ://www.ncbi.nlm.nih.gov/books/NBK500097/.
1,2 The authors wrote that a 2018 survey from the Crohn’s and Colitis Foundation reported that health care professionals expressed discomfort when prescribing biosimilars in the pediatric population compared with adults. One patient started Inflectra in 2016 and 2017. There was a slow uptake of infliximab biosimilar use among the ICN centers.
This has driven a staggering surge in prescriptions, with some reports indicating growth of over 5,000% since 2018 in the United States. Justin Kozak The buzz around GLP-1 agonists like Ozempic and Wegovy is undeniable, fueled by social media virality and impressive clinical results.
Episode 1007: What the New SCCM Sedation Guidelines Say About Melatonin Subscribe on iTunes , Android , or Stitcher The 2018 SCCM guidelines on pain, agitation, delirium, immobility, and sleep have received a focused update which has been published in the journal Critical Care Medicine.
In September 2018, the Indian government banned 328 FDCs after an expert committee found that many lacked therapeutic justification and posed potential health risks. Regulatory actions and concerns Despite their growing adoption, FDCs have been subject to increased regulatory scrutiny due to concerns over irrational combinations.
External Links Ear drops for the removal of earwax, 2018 FDA Takes a Stand Against Ear Candling, 2010 Summary If any ear wax remains despite treatment to soften the wax for 3-5 days, referral for ear irrigation may be advisable.
While this investment led to a seven percent rise in annual apprenticeship starts within the life sciences sector between 2018/19 and 2022/23, industry leaders have consistently argued that the narrow focus on apprenticeships left gaps in training provision. billion in 2017/18 to 2.5 billion in 2023/24.
The rising volume of clinical trials increases demand and competition for patients The number of oncology assets in the clinical development pipeline has increased by 13% annually over five years (2018-2022) 1. On paper, this sounds like a positive time for medical innovation.
Since 2018, the MRI has been tasked with managing MEDISO and has been supporting startups in the drug discovery sector to bring their intellectual property to the market.
Biggest spenders DTC ads are almost exclusively leveraged for brand name drugs, with two-thirds of that spending concentrated on just 39 drugs between 2016 and 2018, according to a Government Accountability Office report. Some of the biggest spenders are shelling out millions to get their brands in front of American audiences.
This approval was followed by Takeda Pharmaceuticals Alofisel (darvadstrocel), which received approval from the European Medicines Agency in 2018 and from Japans Pharmaceuticals and Medical Devices Agency in 2021.
Available from: [link] (2018), Efficacy of long-acting injectable omeprazole (LAIOMEP) in the management of equine glandular gastric disease (EGGD) and equine squamous gastric disease (ESGD). . & Gough, S.L. Pharmaceutical treatment of equine glandular gastric disease: A contextualised review of recent developments.
031), and diagnosis between 2016 and 2018 (OR 1.93, P < 001) as well as 2019 and 2020 (1.88, P < 001). in 2016, representing a period of rapid uptake—and usage was consistently high from 2016 to 2018. 3 The utilization of HER2 therapies increased from 64.6% in 2013 to 80.9%
In 2018, following decades of research and development, the first RNA-based therapy, Onpattro (patisiran), from Alnylam Pharmaceuticals reached the market (10). /Moderna with LNP-delivered mRNA-4157/V940 in combination with Keytruda (pembrolizumab) also for melanoma (8–9). News Release. 3 June 2024. News Release. Intellia Therapeutics.
9 (2018): 1259–1265, [link] [14] LeadingAge and the Strategic Health Information Exchange Collaborative (SHIEC), Health Information Exchange (HIE): A Primer and Provider Selection Guide , accessed June 9, 2025, [link] [15] LeadingAge and SHIEC, HIE: A Primer and Provider Selection Guide. [16] 9 (2018): 1259–1265. 9 (2018): 1259–1265.
However, it flamed out in testing in 2018 and Incyte was forced to pivot research toward other candidates. Early in Hoppenot’s tenure, the answer looked like a cancer medicine called epacadostat, which Incyte believed could become a cornerstone of immunotherapy combinations. Since then, Incyte has had some success building out its portfolio.
The answers below are based on my experience as a reviewer and compliance officer at FDA during the 5-week 2018/2019 government shutdown. During the 5-week shutdown in 2018/2019, PDUFA funding was the most robust and could have funded several months of review operations. What does it mean for FDA staff?
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