Clarivate

MARCH 14, 2024

Three ways Clarivate is closing information gaps and establishing reliable data for improved decision-making To win more funding and plan a course for the future, institutions need to understand how their research programs currently perform. For the first time, researchers could accurately associate their work with a universal ID.

Management 52

Management Government Leads 52

European Pharmaceutical Review

NOVEMBER 10, 2023

US researchers have developed the Geometric Viability Assay (GVA), which has been shown to be a fast, cheap and sustainable method for counting microorganisms. coli) and Salmonella enterica in the lab, researchers found that preparing 96 samples took just five minutes, instead of the three hours required with traditional methods.

Engineering 102

Engineering Pharmaceutical 102

pharmaphorum

SEPTEMBER 5, 2022

Greater use of telehealth services forced by COVID-19 seems to have benefitted people with opioid use disorder (OUD), leading to longer times on treatment and reduced risk of overdose, according to a new study. The authors say that the finding “lends support for permanently implementing access to telehealth services.”

Government 98

Government Medical Patients Leads 98

European Pharmaceutical Review

JANUARY 29, 2024

In the published in 2023, the process and requirements for toxicological risk assessment of medical device constituents is outlined. Also covered in the guideline are “the methods and criteria used to assess whether exposure to a constituent is without appreciable harm”.

Food and Drug Administration 88

Food and Drug Administration Medical Safety Food 88

Copyright Clearance Center

SEPTEMBER 13, 2022

. – CCC , a leading provider of Open Access (OA) workflow solutions, has launched OA Agreement Intelligence , the only agreement modeling solution that enables publishers to prepare, build, and analyze their OA data so that they can create and communicate sustainable and transparent agreements with their partners.

Management 105

Management Leads Marketing 105

European Pharmaceutical Review

JULY 28, 2023

Publication of results of the Phase III SKYLARK study “is a pinnacle moment in treating postpartum depression ( PDD ),” stated Dr Kristina M Deligiannidis, Professor at the Institute of Behavioral Science at the Feinstein Institutes, the trial’s principal investigator, lead author of the paper. At day 45, 61.9

Food and Drug Administration 94

Food and Drug Administration Food Safety FDA 94

European Pharmaceutical Review

SEPTEMBER 8, 2022

Comparing the use of common antiretroviral therapy (ART) regimens in pregnancy suggests that dolutegravir-based regimens have a higher probability of human immunodeficiency virus type 1 (HIV-1) viral suppression at delivery. Moreover, the observed risk of preterm birth was 13.6

Medicine 102

Medicine Safety Physicians Pharmaceutical 102

European Pharmaceutical Review

JULY 17, 2023

New research published in JAMA Health Forum has documented that the US National Institutes of Health (NIH) spent $8.1 billion for phased clinical trials of US Food and Drug Administration (FDA)-approved drugs between 2010-2019. percent of total NIH spending for basic or applied research related to these products.

Food and Drug Administration 90

Food and Drug Administration Training Pharmaceutical Food 90

Clarivate

SEPTEMBER 19, 2023

The Citation Laureates 2023 list has been announced, recognizing a select group of influential, highly cited researchers whose contributions are on par with Nobel Prize recipients. We explore their profound impact on our world and their enduring commitment to the pursuit of knowledge, inspiring the next generation of researchers.

Electronics 111

Electronics Medicine Government Patients 111

European Pharmaceutical Review

NOVEMBER 8, 2023

A paper published by Research Square has described a rapid, simple, accurate and precise high-performance liquid chromatography with diode-array detection (HPLC-DAD) method for levofloxacin determination in liquid pharmaceutical formulations. percent trifluoroacetic acid (18:82 v/v) was used as a mobile phase with a rate of 1.5

Food and Drug Administration 97

Food and Drug Administration Pharmaceutical Food FDA 97

Clarivate

OCTOBER 31, 2023

Our latest Global Research Report from the Institute for Scientific Information (ISI) charts China’s research trajectory and its path of growth, quality and international collaboration. Over the last 40 years China’s research economy has experienced remarkable transformation and growth.

Engineering 75

Engineering Leads Networking Electronics 75

Clarivate

DECEMBER 16, 2021

Research integrity is a key part of our mission at Clarivate to be a trusted, indispensable partner to innovators everywhere. Because of this, we are deeply concerned by potential sources of disruption to the scientific literature and research integrity. Researchers also have their own part to play.

Government 105

Government Doctors 105

World of DTC Marketing

MARCH 28, 2022

Oxford researchers say they have confirmed that alcohol is a direct cause of cancer, emphasizing how their findings reinforce the need to lower levels of alcohol consumption in the population for cancer prevention. ” So now, in addition to obesity, alcohol is killing us. These findings will probably have.

Insurance 249

Insurance Ethics Healthcare Healthcare 249

European Pharmaceutical Review

JUNE 16, 2023

The authors argued that fundamentally, implementation of AI/ML for pharmacovigilance has been hindered by the associated legal framework processes and governance issues. Therefore, this suggests sub-optimal use of ML in pharmacovigilance. However, the paper highlighted the challenges these technologies hold for analytics. Bate et al.

Safety 95

Safety Electronics Medicine Government 95

European Pharmaceutical Review

AUGUST 31, 2023

New research published in the New England Journal of Medicine has indicated that stem cell gene therapy could provide a curative treatment for sickle cell disease (SCD). Autologous stem cell therapy The autologous, hematopoietic stem and progenitor cell (HSPC) product OTQ92 incorporated gene-editing using CRISPR-Cas9 technology.

Food and Drug Administration 111

Food and Drug Administration Medicine Food FDA 111

European Pharmaceutical Review

JANUARY 18, 2024

US researchers have reported promising outcomes from a Phase I/II trial in cancer patients treated with cord blood-derived CD19-targeted chimeric antigen receptor (CAR) natural killer (NK) cell therapy. Published in Nature Medicine , the findings revealed an overall response (OR) rate of 48.6 percent at 100 days post treatment.

Manufacturing 83

Manufacturing Patients Safety Medicine 83

European Pharmaceutical Review

FEBRUARY 15, 2023

The results suggest “that neoadjuvant nivolumab was safe in long-term follow-up,” commented Patrick Forde, MBBCh, an Associate Professor of oncology and Director of the Thoracic Oncology Clinical Research Program at the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins. It was successfully managed, the authors noted.

Food and Drug Administration 93

Food and Drug Administration Patients Food Networking 93

Copyright Clearance Center

JANUARY 17, 2023

RLSC makes it easy for scholarly publishers of all sizes to automate and scale OA institutional agreements and collect publication charges. It is the most widely-adopted, community-led market solution that simplifies OA agreement administration for publishers, funders, institutions, and authors.

Management 52

Management Government Education Training 52

European Pharmaceutical Review

APRIL 3, 2023

In the Phase I New Approaches to Neuroblastoma Therapy (NANT) trial, researchers found that lorlatinib given alone or in combination with chemotherapy was safe and tolerable in patients with relapsed/refractory anaplastic lymphoma kinase (ALK)-driven neuroblastoma. The data showed 63 percent of patients responded to the combined treatment.

Food and Drug Administration 82

Food and Drug Administration Medicine Patients Food 82

European Pharmaceutical Review

AUGUST 23, 2022

A study of the causes of warning letters issued by the US Food and Drug Administration (FDA)’s Center for Drug Evaluation and Research (CDER) and Center for Devices and Radiological Health (CDRH) between 2010 and 2020 revealed that poor current good manufacturing practice (cGMP) compliance and misbranding were the most common citations.

FDA 98

FDA Food and Drug Administration Pharma Pharmaceutical manufacturing 98

European Pharmaceutical Review

JANUARY 11, 2023

The findings, published in Nature Communications , show a wide imbalance in microbiome composition in people with Parkinson’s. The research reported Parkinson’s disease metagenome is indicative of a disease-promoting microbiome. “We Heersink School of Medicine Department of Neurology and senior author on the study.

Medicine 103

Medicine Medical Pharmaceutical Patients 103

European Pharmaceutical Review

MARCH 30, 2023

The first-in-human, Phase I/Ib study published in Nature Medicine , described the interim analyses of the novel delivery approach. Until recently there have been limited resources to develop clinical trials in this space,” commented corresponding author Dr Isabella Glitza Oliva, PhD, Associate Professor of Melanoma Medical Oncology. “We

Side effects 86

Side effects Patients Medicine Leads 86

European Pharmaceutical Review

SEPTEMBER 29, 2022

According to a new report , implementing a Transferable Exclusivity Extension (TEE) system could solve the “broken economic model” for researching and developing new antibiotics in Europe. Table 2 : The cost to healthcare systems of extending the exclusivity of another product using the voucher for each of the six countries.

Medicine 105

Medicine Healthcare Healthcare Patients 105

European Pharmaceutical Review

AUGUST 11, 2022

Hospitalised patients on high-flow oxygen for severe COVID-19 pneumonia were nearly 50 percent less likely to die when treated with antiviral remdesivir in combination with steroid dexamethasone and baricitinib, according to research from Rutgers Ernest Mario School of Pharmacy in the US.

Food and Drug Administration 80

Food and Drug Administration Patients Medical Food 80

European Pharmaceutical Review

JULY 20, 2022

Researchers have shown that ratio of nicotinic acid (NA) to nicotinamide (NAM) in cell cultures significantly increases with the presence of live microorganisms within 24 hours, acting as a useful biomarker for the detection of early-stage microbial contamination in cell therapies. coli -contaminated MSCs after 5.5 hours, respectively.

Distribution 101

Distribution Media Manufacturing Patients 101

Pharmaceutical Technology

MARCH 23, 2023

These changes come following a public consultation with the Healthcare Research Authority, to which a government response was published on March 21. Furthermore, the UK is now implementing a legislative requirement to publicly register clinical trials and share summary results with any research participants.

Healthcare 59

Healthcare Healthcare Recruitment Government 59

European Pharmaceutical Review

SEPTEMBER 8, 2022

“The most exciting finding of the study is the robustness of the signal in the cluster-interval data,” noted co-author and Assistant Professor of Neurology at Harvard Medical School, US, Dr Jurriaan Peters. ” The results of the study were published in Epilepsia. . days in Period 1 (day 1-90) to 26.8

Safety 93

Safety Medical Patients Pharmaceutical 93

European Pharmaceutical Review

JULY 29, 2022

Both the European Medicines Agency (EMA) and US Food and Drug Administration (FDA) have endorsed a statement calling for international collaboration on integrating real-world evidence (RWE) into regulatory decision-making. Interested parties also need to deal with various processes for data sharing and access.

Food and Drug Administration 89

Food and Drug Administration Medicine FDA Food 89

Clarivate

SEPTEMBER 27, 2022

In our blog series about Highly Cited Researchers and the UN Sustainable Development Goals (SDGs), we turn our attention to SDG 6: Clean Water and Sanitation. An example of this came in August, when researchers warned that Europe is facing its worst drought in 500 years. Highly Cited Researchers tackle the water crisis.

Management 98

Management Government Pharmaceutical Networking 98

pharmaphorum

JULY 6, 2022

Yet, three of the 19 drugs given the go ahead in the US were later withdrawn, compared to just one in the EU, prompting some to ask if faster approval times merely represent “quantity over quality”. And how can regulators balance timely access with robust safety? Delayed access. The remaining 12 still have confirmatory trial results pending.

Safety 93

Safety FDA Medicine Patients 93

European Pharmaceutical Review

DECEMBER 21, 2022

Since then, there have been few breakthrough innovations in treating neuropsychiatric diseases such as anxiety, depression, substance use disorders (SUDs), and post-traumatic stress disorder (PTSD). Psychedelic research, in particular, is gaining momentum. . Up until recently, it took a prohibitive stance toward psychedelic research.

Food and Drug Administration 114

Food and Drug Administration Medicine Food Government 114

pharmaphorum

JANUARY 26, 2023

In March, the collaborative T2T consortium published the first complete telomere-to-telomere sequence of the human genome, filling in the last 8% of the 3 billion base pairs that make up our DNA. Moreover, research has shown that genetic testing can reduce adverse reactions to drugs by nearly one third.

Pharmacology 116

Pharmacology Government Leads Physicians 116

European Pharmaceutical Review

MARCH 11, 2024

In fact, a study published in 2023 in The Lancet HIV revealed that women and men with HIV at age 40 had an average of 39 and 37 years of life left, respectively – only a few years less than that of the general population – if they started antiretroviral therapy (ART) after 2015. 3 But that paradigm is rapidly changing.

Medicine 95

Medicine Pharmacology Healthcare Healthcare 95

pharmaphorum

SEPTEMBER 29, 2022

Language matters in every walk of life, and research – where access barriers contribute to systemic health inequalities – is no exception. Yet, new research published by campaign group Demand Diversity, with the support of COUCH Health, found a number of terms in common usage were outdated or even offensive.

Healthcare 59

Healthcare Healthcare Education Training 59

pharmaphorum

NOVEMBER 25, 2022

Scientists in the US say they have developed an mRNA-based vaccine that encompasses all 20 known subtypes of influenza that could form the basis of a future universal jab. The post mRNA can deliver universal flu vaccine, say US researchers appeared first on.

Prospecting 105

Prospecting Manufacturing Medicine Leads 105

Clarivate

SEPTEMBER 21, 2022

Clarivate draws on Web of Science publication and citation data to produce an annual list of Citation Laureates – researchers of Nobel class whose high-impact contributions have transformed their fields and changed our world for the better. Identifying the giants of research. 01%) have been cited 2,000 or more times.

Electronics 111

Electronics Medicine Leads Medical 111

European Pharmaceutical Review

JUNE 27, 2023

difficile in December 2022, the microbiome therapies space in 2023 has continued to see revolutionary developments and continued research advancement. Notably, gut microbiome was found to linked to cancer CAR T therapy response, based data from the largest prospective study of its kind, published in Nature Medicine in March 2023.

Food and Drug Administration 103

Food and Drug Administration Manufacturing Medicine Pharma 103