This page shows the latest safety news and features for those working in and with pharma, biotech and healthcare.
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
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.
prescribing other cannabis-based products as there isn’t enough clinical evidence to support the safety or efficacy.
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
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
MIMS also provides scientific strategy services along with digital medication safety services.
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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
Regulatory oversight of interventional studies has been tasked with ensuring patient safety, while also helping to encourage cost containment through promoting expediency in discovery.
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.
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.
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
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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
clinical research, medical affairs and drug safety.
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
Institute for Highway Safety.
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.
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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
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
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
care and safety in the region.
The market may face few hindrance for high cost of safety syringes and increasing incidence of needle stick injuries.
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