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safety
This page shows the latest safety news and features for those working in and with pharma, biotech and healthcare.
Going digital
Certainly, medical device manufacturers will need to tread a fine line between innovation and patient safety. ... And then there’s the issue of dealing with patient-developed devices and the potential regulatory and safety consequences that could result
Latest news
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Big opportunities in big data, but EMA and industry just getting started
Much may be gained from the rational use of Big Data in a regulatory context for approval and monitoring of efficacy/effectiveness and safety of medicines, medical devices and combinations thereof.
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Medicinal cannabis firm Althea enters UK market
prescribing other cannabis-based products as there isn’t enough clinical evidence to support the safety or efficacy.
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Europe’s medicines tracking system goes live
The European Medicines Verification System (EMVS) is a pioneering system, and is using new technology and a dedicated network of national bodies working together to guarantee safety and security. ... This provides a final safety measure to ensure the end
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No deal Brexit would see UK miss out on ‘safest medicines system in the world’
Health leaders say it would be 'a travesty'. Patients in the UK would miss out on enhanced medicines safety in the event of a no deal Brexit, pharma industry and NHS ... Questions also remain about the UK’s continued access to other important European
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Ashfield partners with MIMS, WA Health wins new account and Lighthouse relocates
MIMS also provides scientific strategy services along with digital medication safety services.
More from news
Approximately 84 fully matching, plus 1,898 partially matching documents found.
Latest Intelligence
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2019: CRISPR and therapeutic gene editing comes of age
Safety concerns. Like any emerging technology, there is still plenty to consider regarding safety as the first human trials start to generate results – even before He’s reckless bid for the
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Immunotherapy combination trials Q&A
Regulatory oversight of interventional studies has been tasked with ensuring patient safety, while also helping to encourage cost containment through promoting expediency in discovery.
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Alzheimer’s disease – is Europe prepared if a breakthrough treatment becomes available?
However, there may be two relatively near-term solutions: building dedicated infusion centres as extensions to existing facilities and using home infusions, if possible based on the therapy’s safety profile.
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AstraZeneca’s oncology renaissance
So how did AstraZeneca achieve this turnaround? In 2010 Mene Pangalos introduced a ‘5R framework’ for R&D: right target, right patient, right tissue, right safety, right commercial potential.
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Five questions guiding the way to actual patient-centricity
We also learned that patients’ trust, encouraged by a better comprehension of our work, has been correlated with better clinical outcomes and features, including drug adherence and reporting of safety concerns. ... For the past decade, the limelight
More from intelligence
Approximately 2 fully matching, plus 132 partially matching documents found.
Latest appointments
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BMS appoints new commercial leader, Davies joins Eisai and more
Officially joining the biopharma on 1 October, Schuermans will play a part in bringing together Sobi’s manufacturing operations/biological development and supply, quality, supply chain, procurement and environment and safety
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Immodulon Therapeutics bolsters senior team
clinical research, medical affairs and drug safety.
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Prof Sir Mike Richards joins Incisive Health as senior counsel
In his most recent role Sir Mike led the inspection, quality and safety agenda for hospitals and prior to that he served in senior clinical roles at NHS England and the
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Eli Lilly appoints senior VP for corporate affairs and communications
Institute for Highway Safety.
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Frequency Therapeutics appoints Steven Dworetzky
Machanda will continue to lead development activities including formulation and analytical development, manufacturing and non-clinical safety studies to facilitate clinical trials and broaden the drug development pipeline.
More from appointments
Approximately 0 fully matching, plus 49 partially matching documents found.
Latest from PMHub
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Clinical Trials Market : Dynamics, Segments, Size and Demand, 2015 - 2025
Request Sample Report@ . Clinical trials are research studies performed on humans to gain specific information about biomedical interventions such as novel vaccines, devices, treatments and drugs and thereby generating safety data. ... Phase I is
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Multi Dose Drug Vial Adapters Market Segments, Opportunity, Growth and Forecast By End-use Industry 2018 - 2028
North America is the most dominating market for Multi Dose Drug Vial Adapters market due to factors such as technological advances, increasing safety awareness and mandatory use of safety devices are
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Intravenous Solution Compounders Market Volume Analysis, Segments, Value Share and Key Trends 2018 - 2028
The rising awareness about the safety of patient and complexity in the compounding of the intravenous solution is anticipated to propel the market growth for intravenous solution compounders. ... APAC is a fast-growing regional market for Intravenous
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Portable Cancer Screen Devices Market Technology Growth and Opportunities 2018 - 2028
care and safety in the region.
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Syringe Scale Magnifiers Market Expected to Expand at a Steady CAGR through 2028
The market may face few hindrance for high cost of safety syringes and increasing incidence of needle stick injuries.
More from PMHub
Approximately 3 fully matching, plus 64 partially matching documents found.
Featured jobs
- Account Manager, Medical Communications and Marketing
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£30, 000 – £40, 000 benefits and bonus
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Senior Medical Writer
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Up to £50, 000 with Benefits
- Editorial Assistant Medical Education Agency
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£25, 000 - £26, 000
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Senior Medical Writer
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Salary TBC
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Digital Account Director
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Salary TBC
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Project Manager/ Account Manager
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Salary TBC
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Account Director, Medical Education
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Salary TBC
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Senior Medical Writer
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Great salary and benefits
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