Express Pharma

DECEMBER 11, 2023

In this article, we delve into the highlights of the Chandigarh Pharma Summit 2023, and showcase the key takeaways and insights from the presentations and discussions at the event. To overcome these hurdles, Dr Gupta advised leaders to collaborate closely with regulatory authorities and proactively address compliance issues.

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European Pharmaceutical Review

APRIL 10, 2025

This article explores the potential impact of the proposal and considers how manufacturers can ensure the safety and reliability of their products. billion Global concerns surrounding PFAS, or per- and polyfluoroalkyl substances, are due to their well-documented effects on human health and the environment.

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Pharma Marketing Network

MAY 9, 2025

This article uncovers the hidden elements of market access success, revealing what it takes to move from FDA approval to formulary inclusion, provider buy-in, and patient adoption. Tools and Partnerships That Enhance Access Market access success isnt just about what you presentits how you communicate it. What is an AMCP dossier?

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ID Stewardship

DECEMBER 13, 2024

In this article an experienced antimicrobial stewardship pharmacist discusses lessons learned from navigating antimicrobial stewardship metrics. BCPS, BCIDP Article posted 13 December 2024 If you cannot measure it, you cannot determine if you have changedit. Disclaimer The views and opinions in this article are those of the author.

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GMPSOP

JULY 14, 2024

This article provides an in-depth look at how you, as a professional in a GMP business, can prepare quality planning documentation, especially from the perspective of a medical device manufacturing business. Additional documents included each month. Documentation control b. Additional documents included each month.

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Proxsys Rx

APRIL 1, 2025

In a nutshell, says ProxsysRx 340B Optimization Manager Chance Spivey, the CE would have to pay retail prices first to allow for replenishment and THEN submit documentation like they do for 340B ESP (this time with even more claims info). Automate your 340B program with customized software streamlining documentation and reporting.

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ID Stewardship

OCTOBER 14, 2024

In this article a pharmacist with experience in writing and publishing provides 5 quick tips for pharmacy residents preparing manuscripts Authored By: Timothy P. BCPS, BCIDP Article Posted October 2024, First Released in the June 2024 IDstewardship Newsletter Tip 1: Start by picking an article type and journal The article type (e.g.,

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European Pharmaceutical Review

OCTOBER 3, 2024

Indeed, a key aspect of EU GMP Annex 1 is the requirement for pharmaceutical manufacturers to develop a comprehensive Contamination Control Strategy (CCS) that documents their approach to assuring the sterile drug product’s high quality and, therefore, enhancing patient safety.

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European Pharmaceutical Review

JANUARY 25, 2024

These standardised documents provide meticulously curated and scientifically approved information. 7 Access to digital communications also remains a challenge in some Member States especially for those groups at risk of poverty and social exclusion (7.6 11 This requirement directly contradicts what is included in Article 63.

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Express Pharma

JUNE 20, 2023

This article outlines the challenges of conducting human immunology research in a developing country. Institutional support, such as expert consultants, essential document templates, and protocols for regulatory submissions, is also vital. However, the spotlight has shifted to unravelling the complexities of the human immune system.

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GMPSOP

AUGUST 11, 2024

To maintain the integrity and safety of these investigational products, you must adhere to Good Manufacturing Practice (GMP), FDA Clinical Trail Guidance Documents , and relevant ISO or EN standards. Additional documents included each month. Additional documents included each month. ensure traceability and compliance.

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GMPSOP

JULY 23, 2023

If you are completely unfamiliar with what is installation qualification then we suggest you read the article Validation in Pharmaceutical Industry first. Installation qualification verifies and documents that all critical aspects of equipment installation adhere to predetermined specifications and manufacturer’s recommendations.

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GMPSOP

OCTOBER 26, 2022

According to cGMP, validation in pharmaceutical industry can be defined as “Establishing documented evidence which provides a high degree of assurance that a specific process will consistently produce a product meeting its pre-determined specifications and quality attributes.” Additional documents included each month.

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Viseven

AUGUST 7, 2024

If you read this article, you probably dream of getting your foot in the door with medical writing. Medical writing refers to creating healthcare-related textual content that aims to improve doctor-patient communication and provide insights on industry topics. Or maybe you are an employer eager to add a medical writer to the crew.

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Pharma Marketing Network

MAY 23, 2025

This article explores the top AI tools pharma marketers are leveraging today to enhance campaign effectiveness, manage risk, and engage patients and healthcare professionals (HCPs) with greater precision. In practical terms, this means fewer legal escalations, faster campaign launches, and improved documentation for FDA or EMA audits.

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Pharma Marketing Network

OCTOBER 13, 2021

Senior Director and Head, Scientific Communications and Operations at Biohaven Pharmaceuticals, shared advice with conference attendees on how to Navigate Getting Noticed, Hired and Promoted in a Virtual World. “Do Over-Communicate. Senior Director and Head, Scientific Communications and Operations at Biohaven Pharmaceuticals.

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Viseven

SEPTEMBER 6, 2024

In our new article, you will learn more about data integrity in the pharmaceutical and life sciences industry and why maintaining it matters so much. Key Principles of Data Integrity In the 1990s, the FDA developed a list of principles of data integrity, which still serve as a framework for working with data and documenting it.

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GMPSOP

JUNE 16, 2023

In this article, we will briefly discuss some essential elements of analytical method transfer, industry best practices, method transfer strategies, method transfer process workflow, and necessary considerations for a seamless transition. Additional documents included each month. All written and updated by GMP experts. Subscribe b.

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National Association of Boards of Pharmacy

JULY 19, 2024

Know how to identify suspect products and have processes in place to quarantine, investigate, and communicate as required. Document the date and the number of relevant full-time equivalent employees (FTEs) for each parent company pharmacy. Know where your current product tracing information (data) is being stored and how to access it.

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Putting Patients First Blog

APRIL 7, 2025

12 To this end, the NHC encourages the FDA to establish clear expectations for how sponsors validate and document AI-driven findings that are submitted as part of the regulatory dossier. Finally, to support transparency, reproducibility, and traceability, the FDA should require thorough documentation of AI model validation and verification.

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Viseven

JULY 26, 2022

In this article, you’ll find more about mobile health app development, its enormous role in HCPs engagement, and the principal outcomes of including mHealth apps in your multichannel or omnichannel marketing strategy. It will streamline HCPs’ workflows, improve their productivity, and maintain communication agility with patients.

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FADIC

JULY 10, 2023

Designed to enhance how you manage tasks and documents and collaborate with your team, Notion AI offers an intelligent and intuitive platform for managing projects, creating databases, and generating insightful reports. is a revolutionary AI tool transforming how businesses and organisations conduct video communications.

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GMPSOP

MARCH 17, 2023

Table of Contents If you are looking for literary help to write an actionable procedure on corrective and preventive action for your workplace or school, this article will be a good place to start. Immediately communicate the incident to stakeholders and initiate an internal laboratory investigation. Consider this scenario.

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GMPSOP

APRIL 19, 2024

This article will provide a practical framework and approach for the Excel spreadsheet validation used in direct or indirect GMP-related activities, empowering you in your decision-making process. Spreadsheets with different levels of GAMP category GAMP 3: These spreadsheets are used solely to produce paper documents. Subscribe iii.

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GMPSOP

MARCH 20, 2024

This article will discuss the general requirements for instrument calibration in production and laboratory testing, which may affect pharmaceutical products’ identity, strength, quality, or purity. Additional documents included each month. Additional documents included each month. Additional documents included each month.

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Pharmaceutical Technology

JUNE 22, 2023

According to the document, this scheme would instead harm patient access to drugs, which will take longer to turn generic. Årdal previously wrote about the voucher scheme in a February 2023 article published in The Lancet. Baraldi was one of the authors of The Lancet article alongside Årdal.

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GMPSOP

DECEMBER 6, 2024

This article explores how to prevent chemical spills, respond to and manage spills, dispose of contaminated materials, report spills, and assign responsibilities to the spill response team. Additional documents included each month. Additional documents included each month. Additional documents included each month.

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Viseven

JULY 11, 2023

In this article, we’ll explore typical cases of healthcare companies using Salesforce, review the functionality of Salesforce CRM and the solutions for different sectors within life sciences and healthcare, and discover how Salesforce supports healthcare companies and communities. Salesforce Healthcare Benefits – Are They Real?

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Proxsys Rx

JULY 10, 2024

The automated approach to optimizing 340B savings & patient care while overcoming manufacturer restrictions NOTE: The purpose of this article is to highlight features and functionality any 340B platform needs to optimize a health system’s 340B savings and revenue.

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Putting Patients First Blog

SEPTEMBER 3, 2024

Furthermore, it is crucial to understand how patients perceive the communication and support they receive from health care providers regarding the management of their medications. Additionally, the NHC recommends including questions that explore how these access challenges were communicated and managed by health care providers.

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The Physician Pharmacist

JULY 30, 2022

In this article we will cover everything you need to know to not only excel during interview season, but build up personal confidence that you will carry throughout your medical career! Accepting Your Interviews : This probably goes without saying, but every single interaction/communication you have with a program can leave an impression.

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Viseven

DECEMBER 13, 2024

Robotic process automation is the answer many have been looking for, and in today’s article, we will take a closer look at what RPA is in the healthcare industry context and how it can help your business thrive. Telehealth is a set of practices and technologies that allow for long-distance patient-doctor communication and treatment.

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Putting Patients First Blog

JULY 2, 2024

As noted in our previous communications, while the NHC would prefer a more traditional Notice and Comment rulemaking opportunity that would ensure the Agency directly responds to stakeholder feedback, we welcome this opportunity to express our reactions to CMS’ thinking on the negotiation program. doi: 10.1016/j.jaad.2020.06.998

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pharmaphorum

NOVEMBER 23, 2020

I saw a statistic in a Health Europe article, published in September this year, which reported that 81% of patients do not feel listened to by pharma companies. Through this outcomes measurement tool, patients keep comprehensive diaries of their condition, documenting what aspects of the disease affect them most. About the author.

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Express Pharma

JUNE 20, 2025

Archive design basis documents for all facility, process, and utility decisions. Treat each deviation, complaint, or EM excursion as a rehearsal for an FDA discussion – document decisions, risk rationales, and CAPAs with inspection-grade clarity. Regularly conduct mock inspections using external or cross-site auditors.

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Viseven

DECEMBER 4, 2024

This article will discuss pharmaceutical validation, its benefits, types, and basic recommendations. It also requires documenting the entire process, from raw material sourcing to product launch. Process design should be based on solid evidence and include thorough documentation. Keep on reading!

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ID Stewardship

MAY 12, 2023

In this article five tips for incoming PGY2 pharmacy residents is provided. BCPS, BCIDP Article posted: 12 May 2023 The ASHP pharmacy residency match phases 1 and 2 have come to a close. Core resources can include society guidelines, ACCP Self Assessment Program chapters , review articles, key specialty books (e.g.,

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