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In this article, we’ll explore 10 innovative trends in pharma marketing that can set you up for success in this rapidly evolving landscape. Companies are investing heavily in digital tools to streamline communication and build stronger connections. Patient-Centric Marketing Patients want to feel heard.
The holistic approach to CCS required by Annex 1 encapsulates primary packaging components and the wider supply chain vital to compliance. Equipping staff with a ‘contamination-control mindset’ through continual education and communication is therefore fundamental if quality measures are to be upheld and enhanced over time.
In this article the host of the Let’s Talk Micro Podcast (Luis Plaza Rios) is interviewed about his experience and learning clinical microbiology using podcasting via the Let’s Talk Micro podcast. I had the pleasure to meet Luis in person and after exchanging some emails we were able to compose this article.
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. 11 This requirement directly contradicts what is included in Article 63.
Part 1 of this article discussed the massive disruptions to medical events caused by the COVID-19 pandemic and how attendees’ preferences have shifted as things have shaken out. Moreover, no attendee data was available for physical symposia, whereas all virtual symposia packages provided full attendee metrics analyses.
You can read part one of this article here. Teams and Zoom became the backbone of communication and firms embraced new ways of working. As a Non-Clinical Assessor at MHRA he assessed non-clinical data packages for new and generic medicines. About the interviewees.
In this article Joanna Carlish, managing director of financial services at Tag Americas , and Robb DeFilippis, Tag Americas’ managing director, life sciences, go head-to-head to discuss marketing within a regulated industry. “A Joanna Carlish. The idea is about really tapping into where the customer is in their journey. appeared first on.
It’s important to always be open and communicative with your travel companions, so everyone is in-tune and on track together. Aureus Medical Group travelers are covered from day one with a comprehensive perks and benefits package that includes: Low-cost, day-one health, vision, and dental. Unlimited loyalty and referral bonuses.
In our latest UK Leaders article Pinder Sahota, UK general manager at Novo Nordisk, tells us how he hopes to bring the NHS and pharma together to improve outcomes in diabetes and other long-term conditions. That’s what we want to inject into Novo Nordisk.”.
All communications, both internal and external, should reflect the brand’s values and personality. This includes everything from the company’s website and social media presence to packaging and advertising. ” Entrepreneur, www.entrepreneur.com/article/314384. References: 1. ” Communiqué, communique.us/creating-strong-brand-identity-pharmaceutical-industry/.
This article provides insight into process maps and data flows in the biopharma industry using the Reference Architecture Model Industry 4.0 The concepts introduced here will be topics for future articles. In the fourth and last step, the defined work packages are executed. The four-step approach is introduced as a methodology.
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This article explores the potential impact of the proposal and considers how manufacturers can ensure the safety and reliability of their products. However, given that PFAS are ubiquitous in the environment from stain-resistant carpets and non-stick pans, to packaging and electronics, to name a few the task is not that simple.
Just like no two travelers are alike, no two recruiters are the same, and you may need to work with a few before you find one with the communication, style, personality, and work ethic that meshes best with yours. Communicate quickly and clearly. . Answer: Yes, it’s perfectly okay to work with multiple recruiters!
If you think that doesn’t happen nowadays, here’s an article about recent counterfeit HIV medications. This tracking involves the use of unique product identifiers, such as serial numbers and barcodes, on drug packaging to track their movement. It also enables precise tracking and tracing of each drug package.
Most of the time they want to pick my brain on where pharmacy is going or what could be possible, so with that being the case, I thought it would be better to put this article together that may help potentially interested parties. Even some of the most recent pitches are very similar to each other I feel. So let's get started!
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There was a small mix up with communication that Oscar had bloods done at school, so we had a couple of messages saying they were doing it at home, when in fact they were doing it at school as usual during term time. But we like these and will continue to use them when needed (ie not when its 27 degrees Celsius outside!).
Pfizer was able to build close to two years of supply of products for the vaccine; it had to quickly scale up for producing billions of doses in a very short period of time, so Pfizer looked to ramp up drug substance, drug product, and packaging in many sites around the world in record time. Celebrate success and milestones. Andres Angelani.
It also bears extra replacement expenses when drugs are discarded due to improper packaging. In this article, the Viseven team aims to explain how pharma procurement works and to cover effective strategies to transform this process at any level, from local campaigns to national health programs.
As you start to explore the process of traveling with Aureus Medical, it’s important to always communicate your anticipated travel timeline with your recruiter. appeared first on Aureus Medical Group’s healthcare blog provides articles and information regarding careers in travel nursing, travel therapy, allied health and more.
In this article, we’ll explore some innovations and improvement opportunities in the science, manufacturing processes, and facilities that produce these therapies. This article primarily addresses manufacture of therapeutic targets at a length of 1,830 nucleotides per molecule, which encompasses most siRNA and ASOs. 1 Moumné, L.,
This article follows part one of our two-part series, where we discussed how Philips designs innovation and digital health solutions for areas of India’s healthcare system where options are sparse. . It’s a package, and sometimes we deploy one or two modules, sometimes multiple modules in a project.
Small Dispensers and the 6/12/2024 FDA Announcement Concerning DSCSA This week’s article on the recent DSCSA postponement comes from PRS Pharmacy Services. The original article can be found HERE. The DSCSA Adventure continues.
This article summarizes an alternate and more functional way to format the QOS presented in Module 2.3. Currently, it takes time and/or communications (e.g., For purpose of illustration used throughout this article, labels have been assigned to each CQA. Direct feedback from the US FDA on this pilot is shared in the discussion.
This article summarizes an alternate and more functional way to format the QOS presented in Module 2.3. Currently, it takes time and/or communications (e.g., For purpose of illustration used throughout this article, labels have been assigned to each CQA. Direct feedback from the US FDA on this pilot is shared in the discussion.
Quotient Sciences supported a standalone DCS classification and formulation development package. This approach saves considerable time and money, as demonstrated in the recent article by the Tufts Center for the Study of Drug Development (CSDD). A recent example of this was for a compound at the candidate selection stage.
Finally, one of the most important attributes of an advanced CCIT method is high sensitivity: can it detect packaging defects as small as 1 micron to provide ultimate assurance of product sterility? Traditional, probabilistic CCIT methods fail to meet many of these criteria. Please check your email to download the Whitepaper.
In this article, we provide an overview of the latest findings. For AAV, three different serotypes were studied (AAV-2, AAV-5, and AAV-8) and a three-plasmid packaging system was used. For lentivirus, a four-plasmid packaging system was used. Please check your email to download the Case Study.
This article presents relevant insights on the current regulatory and technical landscape for decentralized manufacturing, with select examples of current applications, and discusses perspectives on evolving and adapting the current regulations to meet future capabilities. Nature Communications 12, no. Biotechnology Progress 36, no.
This article offers an overview of the CMC requirements for the small molecules product registration process in Latin America. In addition to the COR, some Latin American markets require approval in the COO, which is defined as the country where the drug is manufactured, packaged, or exported from.
This article proposes recommendations for industry and RAs to address the identified problems. 23 Packaging-Related Contaminants Eighteen studies reported contaminants from drug packaging. 28 , 29 , 30 , 31 One key cause was attributed to the incompatibility between the packaging materials and the product.
This article provides background knowledge from literature and data from experiments to enhance the discussion. x, a free and open-source computational fluid dynamics (CFD) software package. m/s), from which five were shown in this article: 0.20 In the setup represented in this article, at higher velocity setpoints (i.e.,
The manufacturer of dexamethasone products recommends withdrawal of anticholinergic agents at least 24 hours before initiation of steroid therapy in its packaging. When to talk to a healthcare provider about donepezil interactions This article is not a complete list of donepezil interactions.
This article discusses a project that explored AI capabilities to leverage the inspection performance on an existing application and gain additional business insights by tackling a real-world challenge. However, AVI machines have a trade-off between the configuration of the AVI sensitivity and the false rejection rate (FRR). Project Scope.
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.,
4 The biopharmaceutical industry is taking steps to increase its environmental sustainability, 5 which begins with identifying and testing alternatives to existing procurement, materials, logistics, equipment, services, manufacturing processes, packaging, and facility design 6 (see Table 1). 7 An integrative (vs. 7 An integrative (vs.
This article explores effective management and oversight processes for accelerated delivery of large-scale programs of work. Firms co-located in a shared building or on a shared campus might also work together to reduce the environmental impact of communal energy streams. You may unsubscribe from these ISPE communications at any time.
In this article, the term “raw material” refers to a material used in the manufacturing and packaging of a drug substance (DS) or a drug product (DP). Finally, the DP is packaged in a suitable container to ensure continued quality. Reader note: This article was originally submitted to Pharmaceutical Engineering® in January 2022.
link] This article aims to provide some insights to help with building organization strategies and action plans for decarbonization and to provide confidence that no-regrets actions can be taken now. solvent selection, inhaler propellant replacement, and packaging design) to employee travel and commute policy (e.g.,
This article discusses types of facilities and design considerations for C>. Different engineering disciplines, such as architectural and process piping, may use different software packages, which can then be combined into a single coordinated model. You may unsubscribe from these ISPE communications at any time.
This article presents a proposed regulatory strategy to help alleviate supply risks for approved therapeutics. The strategy is to provide an appropriate characterization package that demonstrates the alternative filter or resin will not impact product quality, submit it in a PAS, and, if needed, submit a request for an expedited review.
3] You can learn more about the HPA axis and adrenals here in the linked article. Follow package instructions. These signals create communication and function within nerves and muscles, as the electrolytes move in or out of cells. Follow package directions for each supplement.
In this article, we describe the assessment of lag time for global regulatory approvals of postapproval CMC changes for multiple products over a three-year period. You may unsubscribe from these ISPE communications at any time. Bolivia, Hong Kong, Malaysia, Philippines, and Vietnam). Leave this field blank Regulatory Adv Manuf QA
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