European Pharmaceutical Review

JANUARY 25, 2024

Within the EU, patient information leaflets (PILs) are not merely a regulatory requirement but a cornerstone of patient safety. The European Medicines Agency (EMA) underscores the role of digital platforms in disseminating product information electronically. percent as EU average with some Member States as high as 25 percent).

Healthcare 84

Healthcare Healthcare Electronics Safety 84

pharmaphorum

OCTOBER 14, 2022

.” The programme has been set up to develop four devices – an e-paper label, smart wearable sensor, smart pill box, and endo-cutter used in surgical procedures – with funding from the EU’s Horizon Europe programme and support from the Waste Electrical and Electronic Equipment (WEEE) Forum.

Leads 121

Leads Electronics Ethics Healthcare 121

pharmaphorum

JUNE 22, 2022

Pfizer has harnessed the expertise of health data specialist Truveta to provide close monitoring of safety and other signals for its products, including COVID-19 vaccine Comirnaty, almost in real-time. Using the resource, Pfizer can “learn directly from de-identified patient data at an unprecedented pace and scale,” she added.

Pharma 95

Pharma Electronics Safety Medical 95

Pharma Pathway

SEPTEMBER 16, 2022

Venue: Svenska Design Hotels, 56D, Opposite Wipro Gate 5, Electronics City Phase 1, Electronic City, Bengaluru, Karnataka 560100. As part of Covid-19 safety measures, candidates are requested to sanitize their hands at the entrance, Maintain social distance and ware face mask before entering the venue. Link: [link].

Pharma 90

Pharma Electronics Manufacturing Safety 90

MedCity News

FEBRUARY 6, 2024

The manual data population of site folders and electronic trial master files (eTMFs), for example, is time-consuming and poses issues, including limited document security and data privacy, archiving and retrieval difficulties and human error, resulting in up to a 25% failure rate.

Safety 96

Safety Electronics Training Pharmaceutical 96

Pharma Pathway

DECEMBER 5, 2022

Interview Venue: Velankani Tech Park 43, Housur Rd, Electronics City Phase -1, Electronic City, Bengaluru, Karnataka 560100. As part of Covid-19 safety measures, candidates are requested to sanitize their hands at the entrance, Maintain social distance and ware face mask before entering the venue. Experience: 1-12 years.

Electronics 80

Electronics Specialization Engineering Management 80

European Pharmaceutical Review

OCTOBER 19, 2023

EU medicine packs have unique 2D barcodes and serial numbers to enable tracking via an EU-wide electronic system. EMA stated that the pens have batch numbers, 2D barcodes and unique serial numbers from genuine Ozempic packs.

Medicine 96

Medicine Electronics Safety Manufacturing 96

Referral MD

JULY 5, 2022

After implementing the 2009 Health Information Technology for Economic and Clinical Health (HITECH) Act, US clinics were provided sufficient funds to adapt to newer electronic practices in data recording. As a result, 76% of healthcare practices utilized the benefits of Electronic Health Record (EHR) software. What is an EHR?

Electronics 52

Electronics Healthcare Healthcare Medical 52

World of DTC Marketing

NOVEMBER 1, 2021

billion, making it the fastest-growing sector after computing products and consumer electronics (which will grow 18.0% SUMMARY: According to eMarketer, “in 2020, spending on digital advertising in the healthcare and pharma industry will grow by 14.2% to reach $9.53 this year). How reliable is this estimate?

Doctors 227

Doctors Pharma Retail Electronics 227

Pharma Pathway

SEPTEMBER 20, 2022

Venue: Hotel Southend By TGI, Bommasandra, 5th Cross, Vidyanagar, 21, Hosur Rd, Electronic City, Bengaluru, Karnataka 560099. As part of Covid-19 safety measures, candidates are requested to sanitize their hands at the entrance, Maintain social distance and ware face mask before entering the venue. Contact : 9809818187, 8099056599.

Electronics 85

Electronics Biopharma Safety Manufacturing 85

Clarivate

APRIL 4, 2024

adults performed by Clarivate researchers using claims and electronic health record data, data often referred to as real-world data (RWD). The prevalence and co-occurrence of immune-mediated inflammatory diseases (IMIDs) like inflammatory bowel disease and rheumatoid arthritis varies by race and ethnicity among U.S. million U.S.

Electronics 52

Electronics Patients Medical FDA 52

Medgadget

FEBRUARY 23, 2023

The masks can provide protection against airborne viruses for much longer than conventional masks, enhancing the safety of healthcare staff and reducing waste. However, for healthcare staff caring for COVID-19 patients, effective masks are crucial for both personal and patient safety.

Electronics 94

Electronics Safety Healthcare Healthcare 94

Pharma Marketing Network

MAY 15, 2023

With the advent of electronic health records, social media, and other digital sources, pharmaceutical companies now have access to vast amounts of data that can be used to inform their marketing strategies. However, the use of big data in pharmaceutical marketing also poses significant challenges that must be considered.

Pharmaceutical 59

Pharmaceutical Marketing Electronics Media 59

European Pharmaceutical Review

JULY 20, 2022

Withdrawing drugs over safety concerns requires careful analysis of the health benefits and risks by regulators. Monitoring and studying the side effects of licensed medicines is an essential part of drug development to ensure public safety. Six products were withdrawn or revoked for safety reasons during the study period.

Medicine 80

Medicine Safety Side effects Electronics 80

European Pharmaceutical Review

JUNE 16, 2023

Pharmacovigilance and machine learning Applications of ML include analysing social media posts for safety insights, extracting information from clinical narratives in electronic health records (EHRs) and integrating data sources with multiple analytical approaches to provide richer insights. Bate et al.

Safety 91

Safety Electronics Medicine Government 91

Medgadget

DECEMBER 27, 2022

Conventional batteries can pose a safety risk, and if the device is intended to remain the GI tract for a while they could run out of power. So far, the electronics are using primary batteries that have a finite energy budget and cannot function for the long term.”. The problem is power. It only works in the small intestine.”

Electronics 88

Electronics Safety Leads 88

Pharma Marketing Network

MARCH 23, 2023

With the advent of electronic health records, social media, and other digital sources, pharmaceutical companies now have access to vast amounts of data that can be used to inform their marketing strategies. However, the use of big data in pharmaceutical marketing also poses significant challenges that must be considered.

Pharmaceutical 52

Pharmaceutical Marketing Electronics Media 52

European Pharmaceutical Review

DECEMBER 14, 2023

Over the past few years, we have researched the types of evidence used in regulatory decisions for drug product withdrawals due to safety concerns in Europe. But from a safety point of view, observational studies can be more representative of the population the drug will serve.

Safety 113

Safety Medicine Competition Networking 113

MedCity News

MARCH 21, 2023

The DEA touts the change as a way to ensure patient safety, but several telehealth advocates argue it will greatly disrupt access for those who need the drugs — especially at a time when the mental health and substance use crisis is growing.

Prescription 105

Prescription Safety Patients Electronics 105

Referral MD

FEBRUARY 15, 2024

75% of patient information in the US is still exchanged via fax, costing US healthcare billions of dollars yearly…and more importantly, compromising patient safety and provider job satisfaction.” . “The sharing and administrative functions of coordinating healthcare lag decades behind. ” Direct Trust Blog Post.

Healthcare 52

Healthcare Healthcare Healthcare Provider Electronics 52

Pharmaceutical Technology

JUNE 15, 2023

But before pharmaceutical companies can go to market with a breakthrough drug, they need to ensure safety and efficacy through clinical trials. Pharma companies need tools like AI that can reliably improve this percentage without jeopardizing safety. The need for new medical treatments and drugs has never been greater.

Food and Drug Administration 52

Food and Drug Administration Side effects Recruitment Safety 52

Nixon Gwilt Law

APRIL 22, 2024

The rule applies to developers of Certified Electronic Health Record Technology (CEHRT), particularly those who incorporate predictive decision support interventions (DSIs) into their products. Implementation of risk management practices for all predictive DSIs, ensuring their validity, reliability, safety, security, and effectiveness.

Healthcare 52

Healthcare Healthcare Training Food and Drug Administration 52

Pharmaceutical Technology

MARCH 10, 2023

The pharmaceutical freeze-drying systems market is expected to be driven by the integration of smarter technologies in lyophilisation methods such as electron microscopy, biochemistry, and advancement in surgeries.

Pharmaceutical 59

Pharmaceutical Leads Manufacturing Pharmaceutical products 59

European Pharmaceutical Review

SEPTEMBER 2, 2022

To ensure the safety of medicines post-regulatory approval, a risk management plan (RMP) is established. Sophie Jouaville , PhD, is an associate principal at IQVIA, where she works on the design and oversight of non-interventional real-world evidence (RWE) safety and health economics and outcomes research (HEOR) studies.

Food and Drug Administration 76

Food and Drug Administration Medicine Safety Food 76

Legacy MEDSearch

APRIL 17, 2023

a multi-billion-dollar medical device and industrial safety company. Olin Graduate School of Business at Babson College, and a Bachelor of Engineering – Electronics and Telecommunications from Goa University in Goa, India. He has an MBA in Corporate Entrepreneurship and Strategy from F.W.

Engineering 52

Engineering Manufacturing Electronics Medical 52

Legacy MEDSearch

JULY 21, 2023

This first-in-female procedure was approved by the National Agency for the Safety of Medicines and Health Products (or ANSM, the French equivalent to the U.S. Food and Drug Administration). “It’s magic,” the patient stated, as the first woman to activate the novel UroActive device.

Food and Drug Administration 52

Food and Drug Administration Patients Safety Recruitment 52

Clarivate

FEBRUARY 28, 2024

Data from a rising tide of sources can empower pharma executive decision making from R&D, clinical studies, health outcomes, drug safety, and market access.

Electronics 59

Electronics Healthcare Healthcare Medicine 59

European Pharmaceutical Review

MARCH 12, 2024

If data used to support the safety , efficacy and quality of pharmaceutical products is compromised or unreliable, it can lead to regulatory non-compliance, product recalls, and most importantly, harm to patients who depend on those medications. How can this be mitigated? Good documentation practices. What is an effective solution?

Government 89

Government Pharma Ethics Training 89

PM360

AUGUST 9, 2022

Measuring and monitoring adherence in clinical trials would add valuable information about the effectiveness and safety of drugs. Adherence can be measured in a variety of ways, including electronic monitors. via electronic patient-reported outcomes in response to a missed dose). Pill counts, however, overestimate adherence.

Medical 105

Medical Electronics Patients Healthcare 105

PM360

SEPTEMBER 7, 2023

Taking things a step further, using AI to analyze data from sources such as electronic health records (EHRs), wearables, and self-reported patient data could lead to a more preventive and less reactive approach to patient care. “AI/machine

Patients 111

Patients Physicians Healthcare Healthcare 111

Pharmaceutical Technology

OCTOBER 13, 2022

However, the UK’s Electronic Medicines Compendium (EMC) states that “the safety and efficacy of Circadin in children aged 0 to 18 years has not yet been established.” But Reiter supported the safety of melatonin use since it’s a naturally occurring hormone, likening the drug’s status in the UK to “making kidney pie prescription-only."

Prescription 59

Prescription Medicine Safety Sales 59

European Pharmaceutical Review

MAY 17, 2024

Electronic trial master file (eTMF) systems, quality management systems (QMS), master data management (MDM), and enterprise resource planning (ERP) were highest priority for investment. But what needs to happen so that users/process owners can fully trust data’s quality, integrity, reliability, etc?

Government 52

Government Management Electronics Manufacturing 52

pharmaphorum

DECEMBER 22, 2022

For instance, at a recent presentation to the Society of Quality Assurance 2022 Annual Meeting , the FDA Office of Regulatory Affairs Bioresearch Monitoring Division Director Anne Johnson emphasised that DCTs are largely reliant on electronic data integrity and therefore subject to firmly established 21 CFR Part 11 compliance.

FDA 84

FDA Patients Electronics Medical 84

Pharmaceutical Technology

APRIL 20, 2023

Rather than bringing patients to sites, study teams are now exploring ways they can bring the trial to patients using a varying combination of direct-to-patient drug shipments, home nursing, video conferencing, and electronic data collection.

Safety 52

Safety Patients Recruitment Networking 52

PM360

NOVEMBER 12, 2023

New entrants come into a therapeutic class, often with increased efficacy or safety, while older products lose patent exclusivity, changing the promotional landscape. Nowadays, many physician and patient interactions are virtual, and, even when they are face to face, physicians usually rely on an electronic medical records (EMR) system.

Physicians 52

Physicians Media Electronics Pharmaceutical 52

PM360

DECEMBER 14, 2023

Combined, they are having a lasting effect on the reputation of the healthcare sector and the safety and durability of its products and services. Electronic Medical Records in Healthcare. So how should marketers prepare? JAMA Health Forum. 2022;3(12):e224873. doi:10.1001/jamahealthforum.2022.4873. 2022.4873. 2022, February 17).

Healthcare 52

Healthcare Healthcare Marketing Ethics 52

Pharmaceutical Technology

APRIL 13, 2023

Lower DCT usage for Phase I studies may be accounted for due to the heavier focus on safety and efficacy, and increased monitoring of trial participants in-person. In a 2022 poll for GlobalData [7] readers of Pharmaceutical Technology said they believed that wearable technologies and AI carried the promise of improving DCTs the most.

Food and Drug Administration 52

Food and Drug Administration Electronics Healthcare Healthcare 52