Aureus Medical Group

OCTOBER 19, 2022

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.

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The Digital Apothecary

APRIL 26, 2019

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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pharmaphorum

AUGUST 17, 2020

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.

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Aureus Medical Group

JULY 18, 2022

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.

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pharmaphorum

AUGUST 11, 2020

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.”.

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ISPE

NOVEMBER 2, 2022

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.

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pharmaphorum

AUGUST 1, 2022

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.

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IDStewardship

NOVEMBER 29, 2023

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.

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ISPE

OCTOBER 28, 2022

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.

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pharmaphorum

MARCH 16, 2022

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.

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Viseven

SEPTEMBER 14, 2023

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.

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ISPE

MAY 11, 2023

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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ISPE

MARCH 8, 2023

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.

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The Checkup by Singlecare

MARCH 4, 2024

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.

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ISPE

SEPTEMBER 11, 2023

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.,

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ISPE

SEPTEMBER 11, 2023

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.

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The Thyroid Pharmacist

OCTOBER 27, 2023

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.

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ISPE

MARCH 7, 2023

This article reviews two case studies that cover sustainable pack types and extension of shelf life. Case Study One: Packaging Materials The first case study looks at developing more sustainable packaging materials and reducing the size of packaging materials. Let’s use the example of the packaging for medicines.

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ISPE

MAY 9, 2023

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.

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ISPE

MARCH 29, 2023

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.

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ISPE

MARCH 29, 2023

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.

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ISPE

JANUARY 10, 2023

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.

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ISPE

OCTOBER 27, 2022

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.,

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ISPE

MARCH 7, 2023

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.

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ISPE

MARCH 6, 2023

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.,

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ISPE

AUGUST 30, 2022

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.

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ISPE

AUGUST 29, 2022

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.,

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ISPE

MARCH 15, 2023

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.

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ISPE

OCTOBER 27, 2022

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.

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Pharmaceutical Technology

MARCH 29, 2023

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.

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Pharmaceutical Technology

APRIL 14, 2023

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.

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ISPE

SEPTEMBER 10, 2023

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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Pharmaceutical Technology

FEBRUARY 23, 2023

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.

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