Pharma Marketing Network

AUGUST 9, 2023

The pharmaceutical industry operates in a highly regulated environment, where marketing and advertising practices are subject to rigorous scrutiny. Navigating these regulatory challenges is essential to ensure compliance, maintain trust, and effectively communicate the benefits and risks of pharmaceutical products.

Marketing 52

Marketing Pharma Food and Drug Administration Media 52

European Pharmaceutical Review

AUGUST 23, 2022

FAKE MEDICINES are not a new problem, and pose a tremendous threat to patient safety and public health in society regardless of a country’s economic status. 1 Simply, pharmaceutical products are the most vulnerable to counterfeiting. 1 Simply, pharmaceutical products are the most vulnerable to counterfeiting.

Medicine 92

Medicine Food and Drug Administration Pharmaceutical products Pharmaceutical 92

European Pharmaceutical Review

JANUARY 26, 2023

These concentration measurements are used as part of regulatory decisions regarding the safety and efficacy of medicinal products. The post EMA publishes updated Q&A for ICH M10 appeared first on European Pharmaceutical Review.

Food and Drug Administration 90

Food and Drug Administration Medicine Pharmaceutical products Pharmaceutical 90

European Pharmaceutical Review

APRIL 17, 2023

Factors impacting the automation in the biopharma industry market The report found that 75 percent of pharmaceutical organisations want to use automated solutions more frequently. Automated solutions, especially those aided by artificial intelligence (AI) , can enhance product safety, the report noted.

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Biopharma Manufacturing Pharmaceutical products Marketing 92

Pharma Marketing Network

AUGUST 9, 2023

The pharmaceutical industry operates in a highly regulated environment, where marketing and advertising practices are subject to rigorous scrutiny. Navigating these regulatory challenges is essential to ensure compliance, maintain trust, and effectively communicate the benefits and risks of pharmaceutical products.

Marketing 40

Marketing Pharma Food and Drug Administration Media 40

European Pharmaceutical Review

MARCH 12, 2024

In the pharmaceutical/life sciences industries, maintaining data integrity is crucial given its role in making critical decisions that shape outcomes from drug development to human health. What is the biggest impact of having compromised data when working with regulatory bodies in the pharmaceutical industry? How can this be mitigated?

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Government Pharma Ethics Training 90

Contrarian Sales Techniques

FEBRUARY 25, 2023

Clinical studies play an essential role in determining the safety and efficacy of new drugs before they can be approved for the public. In Malaysia, the National Pharmaceutical Regulatory Agency (NPRA) regulates and ensures the safety, efficacy, and quality of pharmaceutical products on the market.

Side effects 52

Side effects Medical sales reps Insurance Pharmacology 52

Pharmaceutical Technology

SEPTEMBER 15, 2022

Packaging plays a vital role in maintaining the quality, safety, user-friendliness and marketability of drugs and other pharmaceutical products. Pharmaceutical Technology has listed some of the leading contract commercial packaging companies, based on its intel, insights and decades-long experience in the sector.

Leads 52

Leads Marketing Pharmaceutical manufacturing Pharmaceutical 52

PM360

DECEMBER 20, 2023

Given China’s status as the world’s second most populous nation and an economic powerhouse, it represents both a monumental market opportunity and a dynamic arena of challenges for pharmaceutical products. At the same time, a “drug lag” persists in China for global pharmaceutical companies’ products. in the U.S.

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Marketing Insurance Medical Manufacturing 105

Pharmaceutical Technology

OCTOBER 28, 2022

Quality by design (QbD) is a concept introduced into the pharmaceutical regulatory lexicon in 2005. QbD principles are woven into regulatory guidance documents, primarily guidances Q8 to Q11 of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH).

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Manufacturing Safety Medicine Pharmaceutical products 52

European Pharmaceutical Review

JANUARY 16, 2023

This Q&A covers the key developments in pharmaceutical microbiology in 2022, featuring insight from pharmaceutical microbiology experts: Dr Tim Sandle, Head of Microbiology, Bio Products Laboratory Limited. What were the main challenges for pharmaceutical microbiology in 2022?

Pharmaceutical 127

Pharmaceutical Food and Drug Administration Manufacturing FDA 127

Contrarian Sales Techniques

DECEMBER 4, 2023

In the bustling world of pharmaceutical sales, the role of a sample bag is often understated yet crucial. Imagine this: a pharmaceutical sales representative, armed with the latest and greatest in medical advancements, sets out to make their mark in the competitive healthcare industry. The sample bag they carry isn’t just a container.

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Sales Pharmaceutical Sales Pharma Ethics 52

eMediWrite

MAY 10, 2022

The pharmaceutical business, on the other hand, is operating at full capacity. ENSURE SAFETY. Make use of social media to promote safety and make people feel safe. Explain how various pharmaceutical products affect the current condition and aid in the fight against infection.

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Media Marketing Pharma Safety 52

European Pharmaceutical Review

DECEMBER 19, 2023

8 A wide range of pharmaceuticals including vaccines have been thermally stabilised to comply with this requirement by being dried from solutions of water-soluble glasses, particularly sugar glasses and most effectively trehalose. Injection Safety Fact Sheet. Novel functions and applications of trehalose. 2002;74 (7):1263–1269.

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Distribution Manufacturing Food Specialization 101

PharmaKinnex

AUGUST 23, 2022

The pharmaceutical industry of 2022 is very different from the space that we all knew in 2012, 2016, or even 2020. More convenience and safety? New drugs are still being developed, approved, and launched with regularity…but unfortunately, many of these new products failed to live up to their full potential. August 23, 2022.

Pharma 52

Pharma Sales Sales Strategy Marketing 52

European Pharmaceutical Review

JULY 25, 2022

While the global trade of fake pharmaceuticals has long been a threat, the COVID-19 pandemic sent the fraudulent market into overdrive. Criminals were able to capitalise on supply chain disruptions, industry regulations being in transition and the urgent global demand for medical products; consequently they thrived.

Pharmaceutical 85

Pharmaceutical Medicine Pharmaceutical manufacturing Manufacturing 85

Pharmaceutical Technology

MARCH 22, 2023

The pharmaceutical industry began using radio frequency identification (RFID) tags in the early 2000s. Various uses soon became apparent including those for supply chain management, anti-counterfeiting, and to improve patient safety. In 2020, Fresenius Kabi introduced their first RFID-enabled medication, Diprivan +RFID.

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Food and Drug Administration Electronics Pharma FDA 105

European Pharmaceutical Review

AUGUST 9, 2022

According to researchers, a ribB -based colorimetric loop-mediated isothermal amplification (LAMP) assay could become a fast and easy-to-perform detection method for testing non-sterile pharmaceuticals for BCC. Burkholderia species are one of the primary causes of non-sterile pharmaceutical product recalls and accounted for 45.3

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Food and Drug Administration Pharmaceutical products Pharmaceutical Pharmaceutical manufacturing 85

European Pharmaceutical Review

OCTOBER 5, 2022

The difference between single-use, non-recyclable and wasteful packaging, and their eco-friendly alternatives, can determine product success – with a third of UK consumers willing to spend more money to receive sustainable products and services. But these combinations cannot be separated for recycling.

Pharma 86

Pharma Safety Pharmaceutical Manufacturing 86

European Pharmaceutical Review

FEBRUARY 1, 2024

Beyond clinical trials, what other challenges are impacting pharmaceutical companies today? That will be our pivotal trial for not just LDL lowering, but also for safety in Phase III, because it is a very large trial. Michael was the cofounding Chief Medical Officer of Omthera Pharmaceuticals in 2008.

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Pharma Patients Pharmaceutical Leads 77

pharmaphorum

SEPTEMBER 28, 2022

Payers must take into consideration not only the clinical efficacy of a drug, but also its safety profile, side effects, and cost-effectiveness, among other factors. There are several barriers that can negatively impact HTA and pricing outcomes, including uncertainty and trials that are not designed with the payers’ evidence needs in mind.

Biopharma 52

Biopharma Side effects Consulting Pharmaceutical products 52

European Pharmaceutical Review

DECEMBER 27, 2023

Second, the production and delivery of CAR T cells necessitates close collaboration between the pharma industry and academic (usually transplant) departments. 10 Benefits of point-of-care CAR T-cell therapy Even after validation of the efficacy and safety of the therapy, two critical challenges remained – affordability and accessibility.

Manufacturing 85

Manufacturing Food and Drug Administration Patients Pharma 85

Pharmaceutical Technology

DECEMBER 15, 2022

Antimicrobial agents can be used both as active pharmaceutical ingredient (API) and as excipients. As an API, they are commonly seen in antiseptic creams for skin conditions like eczema and psoriasis or in antiseptic solutions, and in oral products for treating throat infections, gum pain, and cold sores. Free Whitepaper.

Pharmaceutical 52

Pharmaceutical Manufacturing Pharmaceutical products Media 52

World of DTC Marketing

SEPTEMBER 28, 2020

But what does that billion dollars buy as far as approving the product for market? Under NO circumstances should any pharmaceutical product be allowed into the market without complete and thorough testing. J&J received more than $1 billion from the U.S.

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Food and Drug Administration Pharma Side effects Food 163

Pharmaceutical Technology

APRIL 26, 2023

Packaging plays a critical part in the pharmaceuticals and medical devices industries and is developed with its own set of security standards for the safety of consumers. The document contains detailed information on the providers and their product offerings, alongside contact details to aid your purchasing or hiring decision.

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Manufacturing Medical Food and Drug Administration Pharmaceutical 52

Pharmaceutical Technology

NOVEMBER 30, 2022

A vitally important assay used across various stages of drug development and manufacturing, container closure integrity testing (CCIT) involves evaluating packaging systems to determine their ability to protect the stability and sterility of pharmaceutical products. appeared first on Pharmaceutical Technology.

Food and Drug Administration 52

Food and Drug Administration Pharmaceutical products Manufacturing Pharmaceutical 52

Pharmaceutical Technology

DECEMBER 8, 2022

This process is used to manufacture pharmaceutical products with low molecular weights in large batches within a short timescale. While this is exciting news for the pharmaceutical industry, chemical synthesis presents a number of challenges when it comes to running a manufacturing plant.

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Manufacturing Pharmaceutical Pharmaceutical products Safety 98