Blog: Ask a Student Pharmacist

MAY 12, 2023

Mikal, PhD eomizowh Fri, 05/12/2023 - 11:04 Expand all + Biography Summary The advent and widespread adoption of social media and other forms of computer-mediate communication (CMC) has had a dramatic impact on population health: both good and bad. Health Communication, 1-10. Mikal, J.P., Beckstrand, M.J., Mikal, J.P., Grande, S.W.,

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Communication 52

The FDA Law Blog

NOVEMBER 21, 2022

patients are “first in the world” to receive innovative medical devices that are of “high-quality, safe, and effective” through “early, frequent, and strategic communications between the FDA and medical device sponsors.” Devices in the Safer Technologies Program (STeP) will be included in FY 2026. Food & Drug Admin.,

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Communication FDA 59

Fuld

FEBRUARY 18, 2019

Actions Companies Should Take Today: Learn to use easy AI tools, like email sorting systems and schedulers and ensure that tools are streamlined; Communicate with employee alumni networks to gain a competitive edge with fresh talent.

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Compounding Communication 65

pharmaphorum

JULY 5, 2022

Prior to this, he founded the industry-leading publication, pharmaphorum, in 2009, which also provides broader content communications and marketing services to enable more effective customer engagement.

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Communication 98

The FDA Law Blog

JUNE 14, 2023

In FY 2026 – FY 2027, continue to support products enrolled in previous fiscal years and expand to enroll up to 100 additional products each fiscal year within existing OHTs or expand to additional OHTs, depending on lessons learned from FY 2023 – FY 2025 experience (i.e., up to 125 total products enrolled through FY 2025).

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FDA Communication 45

The FDA Law Blog

JULY 7, 2024

FDA regulations define a complaint expansively, to include “any written, electronic, or oral communication that alleges deficiencies related to the identity, quality, durability, reliability, safety, effectiveness, or performance of a device after it is released for distribution.” [2] report certain device malfunctions, and.

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Labelling FDA Communication Documentation 64

The FDA Law Blog

SEPTEMBER 22, 2024

Complaints FDA discussed how LDT developers should handle the transition from the current Quality System Regulation (QSR)(21 CFR Part 820) to the recently promulgated Quality Management System Regulation (QMSR) that is scheduled to take effect on February 2, 2026. It should be noted that 21 CFR 803.18(b)(1)(ii)

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FDA Communication Labelling 64

DiversifyRx

JULY 11, 2024

The exemption will last until November 27, 2026, for those small dispensers who qualify. Notification If you choose to accept the exemption, the FDA recommends communicating this decision to your trading partners as needed to further facilitate the distribution of products without difficulty or delay.

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Independent Pharmacies FDA Documentation CPhT 52

Viseven

SEPTEMBER 18, 2024

By the end of 2026, the company will be able to analyze two million genomes. Cloud computing facilitates effortless collaboration Cloud computing makes it easier for life sciences companies to communicate and collaborate globally. This innovative approach has brought more than 40 successful drug discovery projects to AstraZeneca.

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Communication Pharmaceutical Companies Pharmaceutical Companies Vaccines 52

PharmaShots

FEBRUARY 22, 2023

In the US, Trulicity is protected by a compound patent (2027) and by biologics data protection (2026).

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Insurance Compounding Dosage Communication 64

The Checkup by Singlecare

OCTOBER 9, 2024

Fiasp is currently not available in a generic version, and the soonest the patent for the brand name may expire is 2026 ; not until after that date would a generic version be expected. The 10 mL (100 unit/mL) vial is $350 without insurance. What is the generic for Fiasp ? Insulin is a critical medication and alternatives are available.

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Insurance Communication 52

PQA

DECEMBER 13, 2024

Results from this two-year project will be shared in 2026. Contact us at Communications@PQAalliance.org for questions about this program. This fall, we launched a pilot to evaluate the effectiveness of pharmacies in improving adult immunization rates through VBAs with payers.

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Communication Patient Care Immunization 52

Hospital Pharmacy Europe

FEBRUARY 17, 2025

This figure will increase significantly in the coming years as all newly qualified pharmacists will be licensed prescribers on the day of their registration from 2026 onwards. of all UK registered pharmacists. Perceptions, challenges and future outlook The broader reception of pharmacist prescribing has been positive but varied.

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Hospitals Patient Care Clinic Management Communication 59

Pharmaceutical Technology

MAY 25, 2023

Analysis estimates that the oncolytic virus market will reach $1 billion by 2026. According to GlobalData analysts oncolytic viruses are a key immuno-oncology development trend to watch in future. Transgene and BioInvent are co-developing the virus under 50:50 costs and revenue collaboration agreement in oncolytic virus development.

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Communication Labelling Vaccines 52

Pharmaceutical Technology

JANUARY 16, 2023

Negotiated prices will not apply until 2026, but the selected medicines for Medicare price negotiations will be unveiled in September 2023. The legislation contains several provisions to lower prescription drug costs, including allowing Medicare to negotiate the cost of selected medicines. Please check your email to download the Report.

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Pharmaceutical Companies Pharmaceutical Companies Communication Hospitals 64

Pharmaceutical Technology

JANUARY 16, 2023

Negotiated prices will not apply until 2026, but the selected medicines for Medicare price negotiations will be unveiled in September 2023. The legislation contains several provisions to lower prescription drug costs, including allowing Medicare to negotiate the cost of selected medicines. Please check your email to download the Report.

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Pharmaceutical Companies Pharmaceutical Companies Communication Hospitals 52

The FDA Law Blog

FEBRUARY 13, 2025

The update procedures should include how the AI-DSF modifications will be implemented and communicated to end users. Post-market surveillance plans and procedures (PMS) are a requirement under ISO 13485 which will be adopted into FDAs Quality Management System Regulation in 2026.

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FDA Documentation Labelling Method Validation 71

The FDA Law Blog

FEBRUARY 20, 2025

FDA had been scheduled to hold a webinar on the Stage 2 (May 2026) requirements related to the investigational device requirements for LDTs later this month. This inability to consult external experts could make communicating with FDA on important topics of safety and effectiveness even more challenging.

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FDA Communication Labelling 102