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This pharmaphorum webinar, held in association with the National Institute for Health Research (NIHR), takes place on Wednesday 16 th December, 11:00 GMT / 12:00 CET and will look at how to navigate the compliance pathway to increase patient engagement with clinical trials. Gaining patient input on marketing and recruitment materials.
The document from the Prescription Medicines Code of Practice Authority (PMCPA) arrives in the wake of several cases where drugmakers made promotional statements on social media platforms – including LinkedIn and Instagram – that were deemed to have breached the code of practice laid down by the Association of British Pharmaceutical Industry (APBI).
Conversion Rate: Tracks how many users complete a desired action, such as signing up for a webinar or downloading whitepapers. Offer incentives like exclusive research reports or webinar invites. Cost Per Click (CPC): Determines how much is spent for each click on the ad.
In a recent webinar from pharmaphorum, the National Institute for Health Research (NIHR) outlined why and how it has developed a new approach to engage with patients while complying with national regulations, such as those set out in the Association of the British Pharmaceutical Industry’s (ABPI) Code of Practice.
That was among the key messages from speakers at a joint European Forum for Good Clinical Practice (EFGCP) and the European Federation of Pharmaceutical Industries and Associations (EFPIA) webinar, held last week. This should cover the entire process, “starting with the writing, the review of the document, and its dissemination”.
Among the recommendations are that more public money should be made available to mental health tech start-ups to encourage the sector to grow, and efforts should be made to build consortia between companies, the NHS digital innovation agency NHSX, medical charities, and government, according to the document.
These documents provide current evidence-based contraception recommendations for health care providers. App for Apple App for Android Webinar with more details coming soon ! We will be hosting a live webinar with continuing pharmacy education credit to review the updated guidelines. MEC) and the 2024 U.S. The goals of the U.S.
The PQA Quality Essentials Webinar series provides education on the fundamentals of quality measurement, which is important for effective measure implementation and performance, and information about where and how PQA quality measures are used. You can listen to the full recording of this Quality Essentials Webinar on PQA’s YouTube channel.
Speakers at a recent Patients as Partners webinar on the document welcomed its publication, and explained how community and collaboration were the keys to turning theory into practice. While the FDA document is rich in the “whys” of greater diversity in research, however, it was lacking in the “hows”, said the speakers. “It
In support of this goal, PQA has performed a review of its bylaws and proposes revisions which modernize and streamline this important governing document. Your Next Engagement Opportunities Network, Learn and Collaborate with PQA Join us for the next PQA Quality Forum Webinar on Thursday, December 7, 1-2 pm ET. Register today!
The PQA Quality Forum Webinar is a regular, recurring series on healthcare quality topics with a focus on medication use and medication services. Priyasha Sarna, PharmD, BCPS, CDCES, Clinical Pharmacist Program Leader, opened the webinar by describing the current opportunity in the U.S.
Today, we published the 2024 PQA Annual Report, which documents our progress towards our strategic goals. PQA Quality Forum Webinar, on October 10, from 1-2 p.m. Members-Only Quality Forum Webinar, on November 21, sponsored by PQS by Innovaccer. 2024 PQA Leadership Summit, November 7-8 in Arlington, Va.
Webinars – Webinars, whether live streamed or on-demand, can be used for communication with HCPs, HCOs, and POs. A company is responsible for the content of webinars and should take reasonable steps to ensure the audience is targeted and well defined.
Helpful practitioner prescribing guidance is set forth in a simplified document here. We will release exciting details of our upcoming webinar addressing telemedicine soon. Stay tuned.
The PQA Quality Forum Webinar is a regular, recurring series on healthcare quality topics with a focus on medication use and medication services. The second edition of the guide documents real-world SDOH services that are promising for improving the quality and safety of medication use.
We continue to play a central role in driving meaningful improvements and positive changes related to medication safety, adherence and appropriate use.The 2023 PQA Annual Report documents our progress towards Blueprint PQA 2025. This webinar is supported by PerformRx. Register today!
Learn more and access PQA's new FAQ document below. In addition to the PQA SDS Risk Adjustment FAQ document, the March 16 PQA Quality Essentials Webinar detailed risk adjustment in quality measurement and provided an overview of the shifts in thinking related to risk adjustment.
Strengthen requirements for standardized documentation and reporting related to the quality of MTM services. Increase stakeholder education about the use of the Medication Therapy Problem Categories Framework to assist with standardizing documentation. You can read more about each of these in the draft call to action document.
We have 19 committees, councils, and working groups that are doing incredible work bringing visibility to the industry’s regulatory challenges and developing solutions that are delivered through ISPE content outlets: webinars, PE magazine articles, iSpeak blog posts, training materials, conference sessions, and ISPE Guidance Documents.
The PQA Quality Essentials Webinar series provides education on the fundamentals of quality measurement, which is important for effective measure implementation and performance, and information about where and how PQA quality measures are used. PQA members can access the presentation slides on the Member Resource Library.
Events sponsored by an accredited CME provider include national, regional, or local conferences, workshops, seminars, journal clubs, simulation labs, and live webinars. This includes print, audiovisual, and internet materials such as podcasts; CD-ROMs; DVDs; archived webinars; CME question banks ; and other web-based activities.
PQA has a new frequently asked questions (FAQ) document that addresses background and basics of SDS risk adjustment and PQA’s risk adjustment recommendations for the three adherence measures in Medicare Part D (PDC-Diabetes All Class, PDC-Renin Angiotensin System Antagonists, and PDC-Statins).
But the EU draft document says that the changes will make medicines more affordable, improve unequal access to medicines across the EU, and fulfil unmet patient needs. EU competitiveness Moll said the legislation revisions should instead be used to make Europe more attractive to pharma companies.
On the technology end, apps, videos, social media, webinars, websites and other tools reach patients wherever they are. Save the date for the next Quality Essentials Webinar on September 20, 1:00-2:00 pm ET. Initiatives include informational leaflets to one-on-one sessions with specially trained pharmacists and dietitians.
Pharmacists must be familiar with billing codes, insurance coverage policies, and documentation requirements to facilitate seamless transactions and ensure fair compensation for their services.
For changes requiring approval before implementation, once the necessary information has been submitted across regions, each health authority must review the data package and documentation based on local requirements. laboratory notebooks, batch records, and technical reports) to submission documents (e.g., Accessed 7 September 2021.
Workplace environments must support ‘psychological safety and [enable] individuals to feel confident, supported and empowered to speak up and raise patient safety incidents without fear’, the document added. To support the publication of the updated patient safety professional standards, the RPS has launched a resources page.
Offering Resources to Implement Point-of-Care Testing The National Community Pharmacists Association and National Alliance of State Pharmacy Associations have developed a new guidance document to help community pharmacy teams with their point-of-care testing services. "A The registration link is in the Member Resources Library.
My primary role is to work with more than 20 ISPE Communities of Practice (CoPs) and Special Interest Groups (SIGs) that generate much of the key ISPE output: Guidance Documents, webinars, PE magazine articles, iSpeak Blog posts, training materials, and conference content.
Your Next Engagement Opportunities Network, Learn and Collaborate with PQA Save the date for the next PQA Quality Forum Webinar, July 20, 1-2 pm ET. data sources), and usability. Additional information about this PQA Convenes event will be shared by August.
Omnicell continues to collaborate with ISMP to improve pharmacy-nursing efficiency, reduce medication errors during dispensing, and support accurate medication tracking and documentation of inventory and deter drug diversion. Watch this webinar to learn more about how automated dispensing systems support ISMP guidelines for medication safety.
As acknowledged in the Strategic Priorities document, certain demographic groups may have limited access to necessary treatments and diagnostics. For those who are interested in learning more about the decentralized clinical trial draft guidance, please check out the FDA’s webinar on June 20, 2023.
Hospitals are already using Fresenius Kabi Simplist® MicroVault® prefilled syringes to help nurses spend less time preparing doses and documenting waste. Watch the "Industry Partnership for Better Controlled Substance Management" webinar on the Omnicell Illuminate 2021 replay page to learn more.
In the years leading up to 2022, numerous publications were issued; networking events, webinars, and conferences were held; and regulatory panel discussions with regulators performed. Is the vendors’ documentation complete in order to assess GxP risks and GxP compliance? and management communication strategy.
Join our next Awesome Webinar Series with guest legal guru JD from Real Value Rx to answer any questions you have about the DSCSA delay. To be authorized: Pharmacies should ensure they receive, maintain, and update these documents as necessary to continue ordering from their ATP and be ready to provide copies of them upon request.
By Philip Won & Véronique Li, Senior Medical Device Regulation Expert — As we recently blogged , FDA released three draft guidance documents to help enhance the predictability, consistency, and transparency of the 510(k) program. One of these documents focuses on “ Evidentiary Expectations for 510(k) Implant Devices.”
Document and Share Experiences: As mentors, it’s essential to document our experiences and share them with the community. This can be through blogs, webinars, or even informal gatherings where we discuss our successes and failures. A great place to learn is our BLOG.
CROs and sponsors use remote source document verification, as approved by the regulator pre-war. Further details: For a first-hand account of managing clinical trials during the war in Ukraine, watch this webinar-on-demand: [1] [link]. Using technology and decentralisation has also contributed.
During the October 31, 2023 webinar discussing the proposed rule, stakeholders sought clarity from FDA officials on the Agency’s plan to address the resource gap. OHT-7’s well documented meltdown during the COVID-19 public health emergency should serve as an object lesson. 24] These submissions all related to a single disease.
PQS will continue to provide educational webinars, resources, and guidance on details surrounding our much-anticipated launch of the new EQUIPP®. We believe that the evolution of the EQUIPP® platform will further those developments allowing for access to streamlined data to be used to the advantage and progression of the healthcare industry.
Mass spectrometers enable complete documentation of the freeze drying process. Learn more about the importance of accurate pressure monitoring in lyophilisation by watching the webinar below. Alternatively, the company can provide calibration pumping stations for on-site adjustment. Process gas monitoring.
This feedback was gathered via surveys and then further discussed by pilot participants during three collaborative webinars. Barriers to Optimizing TAT Prior authorizations are often responsible for longer TAT, with many participants expressing the burden of rigorous documentation required by payers. Want to Learn More?
International convergence is another area in which the FDA is a participant, including in initiatives related to viral safety (ICH Q5A), CM (ICH Q13), quality risk management (QRM; ICH Q9), analytical procedure development (APD; ICH Q2/14), pharmaceutical product life-cycle management (ICH Q12), and common technical document (ICH M4Q).
For example, going “paperless” and moving all of the documentation to the cloud and keeping only electronic documents from now on can be considered a part of digital transformation. To learn more about customer-centric digital transformation, visit our website for exclusive guides, webinars, and events.
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