European Pharmaceutical Review

DECEMBER 22, 2022

The success of mRNA vaccines against SARS-CoV-2 has quickly catapulted mRNA therapeutics as a disruptive, expanding drug category” The term ‘mRNA’ has become commonplace globally. The success of mRNA vaccines against SARS-CoV-2 has quickly catapulted mRNA therapeutics as a disruptive, expanding drug category.

Medicine 111

Medicine Food and Drug Administration Transportation Distribution 111

Pharmaceutical Technology

FEBRUARY 16, 2023

The collaboration will combine the Optejet dispensing technology of Eyenovia with the APNT nanoparticle formulation platform of Formosa to develop topical therapeutics. The Optejet microdose formulation and delivery platform use Microdose Array Print (MAP) technology for delivering 6ml-8ml of the drug.

Food and Drug Administration 59

Food and Drug Administration Food Pharmaceutical FDA 59

pharmaphorum

OCTOBER 12, 2022

Sustainability for Injectable Delivery Devices. Sustainability for Injectable Delivery Devices. Connected Drug Delivery Devices. Hear about new technological advances in the delivery of large volume drugs. Marc Moal, Corporate Programme Vice President, Devices and Delivery Solutions, Novo Nordisk.

Engineering 52

Engineering Safety Consulting Medical 52

Pharmaceutical Technology

MAY 5, 2023

The US Food and Drug Administration (FDA) has accepted Optinose’s supplemental new drug application (sNDA) for Xhance (fluticasone propionate) to treat chronic rhinosinusitis, which is now under review. The regulator has set 16 December 2023 as a prescription drug user fee act (PDUFA) target goal date.

Food and Drug Administration 52

Food and Drug Administration FDA Physicians Prescription 52

Pharmaceutical Technology

AUGUST 2, 2022

GreenLight’s process from formulation of the drug substance and lipid nanoparticle to bulk drug product can be carried out in this facility. The RNA platform of Samsung Biologics permitted GreenLight to move from mRNA vaccine conceptualisation to the delivery of released clinical trial material in under two years.

Engineering 104

Engineering Manufacturing Pharmaceutical 104

European Pharmaceutical Review

JANUARY 29, 2024

1 Some five years after the initial NDMA (N-nitrosodimethylamine) contamination issue 2 initially affecting valsartan drug substance, then other active pharmaceutical ingredients (APIs), eg, sartans, ranitidine, metformin, etc; the toxic short alkyl chain N-nitrosamine issue appears, if not resolved, then well on the way to resolution.

Pharmaceutical 103

Pharmaceutical Food and Drug Administration Medicine FDA 103

Pharmaceutical Technology

APRIL 4, 2023

Gennova Biopharmaceuticals has applied for an emergency use authorisation (EUA) from the Drug Controller General of India (DCGI) for its mRNA-based Omicron-specific Covid-19 booster vaccine. Dubbed GEMCOVAC-OM, the needle-free vaccine will be delivered intradermally with the PharmaJet Tropis Precision Delivery System (PDS).

Safety 59

Safety Distribution Leads Pharmaceutical 59

European Pharmaceutical Review

NOVEMBER 11, 2022

A paper, published in the European Journal of Pharmaceutical Sciences identified the quality assurance (QA) challenges and trends of analytical techniques in ocular drug delivery and formulation, focusing on treatments for glaucoma. seven covered testing in combination drugs. for latanoprost.”

Pharmaceutical 95

Pharmaceutical Safety Medicine 95

Pharmaceutical Technology

OCTOBER 19, 2022

It has combined expertise in otology, gene therapy and inner ear drug delivery to meet the requirements of individuals with disabling hearing loss globally. Topic sponsors are not involved in the creation of editorial content. AK-OTOF is the lead product candidate of the company.

Pharmaceutical 119

Pharmaceutical Medicine Leads Medical 119

Clarivate

SEPTEMBER 19, 2023

Finally, we look at recent Nobel Prizes and judge whether the topics identified would likely receive attention within next few years. Although we do not forecast a topic or researchers for the Nobel Prize in the year we name them Citation Laureates, we do try to anticipate near-term awards.

Electronics 111

Electronics Medicine Government Patients 111

Pharmaceutical Technology

MAY 24, 2023

The AMP programme is a public-private partnership between a number of biopharmaceutical and life sciences companies, the US Food and Drug Administration (FDA) and the National Institutes of Health (NIH), along with non-profit and other organisations. Topic sponsors are not involved in the creation of editorial content.

Food and Drug Administration 96

Food and Drug Administration Manufacturing FDA Food 96

European Pharmaceutical Review

OCTOBER 5, 2023

What are the key topics you plan to cover during your session at CPHI Barcelona? I firmly believe that manufacturing plays a pivotal role in this endeavour, and I will delve into topics such as production system optimisation and the standardisation of chemistry, manufacturing, and control (CMC) processes.”

Manufacturing 91

Manufacturing Consulting Patients Marketing 91

Pharmaceutical Technology

APRIL 21, 2023

Samyang Holdings Biopharm Division CEO Young-Joon Lee stated: “LG Chem has exceptional research and development expertise in innovative drug development and a number of promising new drug pipelines. This is expected to shorten the development time of new drugs and to support personalised treatments.

Patients 52

Patients Leads Pharmaceutical 52

pharmaphorum

NOVEMBER 1, 2022

Further topics to be examined comprise of novel RNA modalities encompassing self-amplifying RNA, saRNA, circular RNA, lnc RNA and many more. Benefits of attending: Explore how mRNA leads the way in the genetic medicine space as the next generation of novel drug modalities.

Pharmacology 52

Pharmacology Medicine Networking Pharma 52

Pharmaceutical Technology

MAY 15, 2023

The US Food and Drug Administration (FDA) has given orphan drug designation to SiSaf’s siRNA [a double-stranded RNA molecule that is non-coding] therapeutic, SIS-101-ADO, for the treatment of autosomal dominant osteopetrosis type 2 (ADO2), a rare and serious skeletal disorder in children.

Food and Drug Administration 52

Food and Drug Administration FDA Food Leads 52

Pharmaceutical Technology

SEPTEMBER 29, 2022

Scribe’s CasX-Editors (XE), a suite of custom engineering genome editing and delivery tools based on new foundations such as the CasX enzyme, will back Sanofi’s developing NK cell therapies pipeline for cancer. Topic sponsors are not involved in the creation of editorial content.

Engineering 52

Engineering Pharmaceutical Sales 52

pharmaphorum

OCTOBER 28, 2022

Nina’s role is to ensure that patients have faster access to the most promising new treatments, taxpayers get better value for money in drug expenditure and the route to funding is speeded up for responsibly priced, promising drugs. Sean Richardson , VP & General Manager UK & Ireland, Alexion. Sean Richardson.

Medicine 112

Medicine Management Marketing Leads 112

Pharmaceutical Technology

NOVEMBER 21, 2022

Additionally, the wide-ranging expertise of RVAC in mRNA, vaccine and drug delivery technologies, and its capabilities in research and development (R&D), biopharmaceutical manufacturing, clinical development and marketing is leveraged under the partnership. Topic sponsors are not involved in the creation of editorial content.

Medicine 52

Medicine Manufacturing Pharmaceutical Leads 52

Pharmaceutical Technology

APRIL 4, 2023

The company will undertake a technology transfer and feasibility study for a drug product focused on the treatment of IPF at its centre of cell and gene expertise in Milan, Italy. Topic sponsors are not involved in the creation of editorial content. Cell & Gene Therapy coverage on Pharmaceutical Technology is supported by Cytiva.

Medicine 52

Medicine Patients Management Leads 52

Clarivate

JUNE 29, 2023

As when any new technology appears on the horizon, a tremendous amount of overheated hyperbole has dominated coverage of the topic in the months since. Clarivate was an early adopter of AI technology that enables researchers to optimize treatment development from early-stage drug discovery through commercialization.

Patients 98

Patients Safety Healthcare Healthcare 98

Pharmaceutical Technology

AUGUST 24, 2022

According to the deal, Lacerta will oversee the discovery of the capsids, as well as their screening and validation, while Prevail will carry out the preclinical and Investigational New Drug-facilitating studies with therapeutic payloads. . Topic sponsors are not involved in the creation of editorial content.

Medicine 52

Medicine Pharmaceutical Sales Marketing 52

Pharmaceutical Technology

OCTOBER 18, 2022

Moderna has entered an agreement with Gavi, the Vaccine Alliance, with regard to the delivery of Covid-19 vaccines to lower-income countries supported by the Gavi COVAX Advance Market Commitment (AMC). In August, the company sought emergency use authorization (EUA) from the US Food and Drug Administration for mRNA-1273.222, its BA.4/BA.5

Food and Drug Administration 52

Food and Drug Administration Food Pharmaceutical Leads 52

Pharmaceutical Technology

JUNE 8, 2023

Both the aerosol delivery and the therapy itself were well tolerated, with no related adverse events. The next month, the US Food and Drug Administration (FDA) placed the program on hold. Topic sponsors are not involved in the creation of editorial content. The company plans to provide an update on this program in H2 2023.

Patients 98

Patients Food and Drug Administration Food Safety 98

Pharmaceutical Technology

MARCH 3, 2023

“The Halle customer service team is a “one-stop-shop” for client requests when it comes to commercial drug product manufacturing,” explains Dragitsch. The batch release process itself incorporates different sub-processes to be followed by different departments.

Specialization 52

Specialization Management Manufacturing Biopharma 52

European Pharmaceutical Review

SEPTEMBER 25, 2023

Of particular interest is the potential of using NMR relaxometry as a point of receipt technique to satisfy regulatory identity testing requirements for active pharmaceutical ingredients (API) and drug product materials. Validation of capillary zone electrophoretic method for evaluating monoclonal antibodies and antibody-drug conjugates.

Pharmaceutical 98

Pharmaceutical Manufacturing Food Electronics 98

pharmaphorum

JUNE 30, 2022

At the 2022 Drug Information Association (DIA) annual meeting last week, it was inspiring to connect with fellow research and development (R&D) stakeholders, regulators, health and digital data partners and more to navigate challenges in drug development that impact patients globally. Delivery models. Patient journey.

Patients 64

Patients Recruitment Transportation Healthcare 64

Pharmaceutical Technology

JANUARY 12, 2023

The collaboration will use the vector biology, manufacturing capabilities and the drug development experience of Solid Biosciences and Phlox Therapeutics’ knowledge in genetic cardiomyopathies and RNA therapies. Topic sponsors are not involved in the creation of editorial content.

Manufacturing 52

Manufacturing Pharmaceutical Patients Medicine 52

PM360

DECEMBER 14, 2023

The downside to this potent drug is it can be quite toxic and poses risks to the human body even in small doses. Some commonly unknown topics touched upon are how sound reaches the brain, what noise-induced hearing damage looks like, and how tinnitus really affects the ear. The videos can be viewed at www.gn.com/inside-the-ear.

Healthcare 52

Healthcare Healthcare FDA Education 52

PM360

OCTOBER 13, 2023

Fine-tuning models can target domains and generate prompts to tag the content into relevant topics. These content topics can then be utilized to create message sets containing information that is pertinent to a specific channel and topic.

Marketing 64

Marketing Specialization Healthcare Healthcare 64

PM360

DECEMBER 14, 2023

Personalized news scans ensure clinicians get the latest news, drug updates, and guideline analyses to support day-to-day practice, while roundtables, discussions, and podcasts offer perspectives on practice trends and innovations from leading community and academic thought-leaders.

Physicians 52

Physicians Pharma Medical Patients 52

Contrarian Sales Techniques

JANUARY 23, 2024

It delves into the science behind the drugs, equipping you with knowledge of anatomy, physiology, and therapeutic areas. Master the art of time management: Craft a realistic study schedule, allocating dedicated blocks for specific topics. Imagine a treasure map, guiding you through the pharmaceutical jungle. Salary expectations?

Pharmaceutical Sales 52

Pharmaceutical Sales Pharmaceutical Sales Ethics 52

Pharmaceutical Technology

APRIL 5, 2023

More than a decade after the first patient was treated with a CAR-T therapy, six therapies relying on the same principles have been approved by the US Food and Drug Administration (FDA) and marketed to thousands of patients. We also have the challenge of delivery. Topic sponsors are not involved in the creation of editorial content.

Food and Drug Administration 59

Food and Drug Administration Engineering Patients Education 59

Clarivate

DECEMBER 14, 2021

2021 surveys of patients and physicians in the United States conducted by Clarivate show that: Much of care delivery has gone virtual. 2021 study had researched prescription drug topics online in the past year. Physicians indicate that nearly 1 in 4 patient consults (23%) are now performed virtually. hours seeing patients.

Pharma 52

Pharma Healthcare Healthcare Physicians 52

Clarivate

NOVEMBER 17, 2021

Mike Ward: Celine, what’s your take on this topic? They’re here to ensure that their company meets the regulatory requirements in the different activities of the organization, whether they are from the submission, to the manufacturing or even the advertising of the given drugs or other pharmaceutical products.

Pharma 52

Pharma Healthcare Healthcare Specialization 52

pharmaphorum

JANUARY 27, 2023

Late last year, pharmaphorum caught up with Dr Karen Mullen, chief medical officer and VP of clinical & medical affairs at global drug development consultancy Boyds. We talk a lot in clinical trials and drug development about benefit,” Dr Mullen said. But who is benefitting?

Patients 96

Patients Pharmaceutical Medical Physicians 96

Clarify Health

NOVEMBER 1, 2019

It is also important to look at the underlying metrics driving these costs, such as post-acute care usage and expensive drug prescribing patterns. When online shopping, you need to understand shipping and delivery time and rates. To learn more about this topic, download our Network Design Playbook.

Networking 52

Networking Retail Insurance Patients 52

Silver Line CRM

MAY 27, 2020

Even that is less relevant now given the nature of today’s specialty drugs (e.g. HCPs are consumers in their personal lives — so they have high expectations around technology and delivery mechanisms that provide a personalized and timely customer experience along with their solution. biologics) that can’t just be dropped off. .

Marketing 52

Marketing Sales Pharma Distribution 52