Pharmaceutical Technology

DECEMBER 16, 2022

The pharmaceutical industry must improve its environmental footprint by investing in technology and expertise, as well as through better design of new drugs early in their development, according to a GlobalData survey of the pharmaceutical industry. This is a particular problem for highly potent drugs such as antibiotics.

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Pharmaceutical Manufacturing 64

European Pharmaceutical Review

SEPTEMBER 22, 2022

Moreover, pharmaceutical manufacturing poses a huge detriment to the state of the planet’s ecosystem. Active pharmaceutical ingredients (APIs) are particularly impact intensive, soaking up a large quantity of resources in terms of heat, energy and water when being produced.

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Pharmaceutical Manufacturing 104

European Pharmaceutical Review

DECEMBER 15, 2022

At least one million people living with type 1 and type 2 diabetes in low- to middle-income countries (LMICs), mainly Africa, are set to benefit from Eli Lilly and Company and manufacturer EVA Pharmaceutical’s new collaboration delivering a sustainable supply of high-quality, affordable human and analogue insulin to this population.

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Diabetes Packaging Communication 86

Express Pharma

MAY 9, 2023

Whereas proper disposal of unused medications, as well as initiatives to reduce packaging waste, chemical waste, and improve recycling programmes, will aid in pro-actively addressing this challenge. This can include equipment with low energy consumption, energy-efficient HVAC systems, and eco-friendly materials.

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Packaging Labelling Pharmaceutical Manufacturing Research Laboratories 91

Quality Matters

JUNE 6, 2023

Despite being called “inactive” ingredients, excipients in medicines play a vital role in drug development, delivery, effectiveness, and stability. That means they can be essential not just for helping to deliver the API to the body, but for ensuring a medicine will work as intended to achieve its therapeutic effect.

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Dosage Packaging Documentation Drug Development 52

Pharmaceutical Technology

AUGUST 10, 2022

Companies should request evidence that the provider can deliver on time, within budget, and that they have the resources and expertise to successfully meet set project milestones.??. Any product sensitives, API configuration, time out of refrigeration (TOR) limits??? appeared first on Pharmaceutical Technology.

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Packaging Communication 52

Quality Matters

SEPTEMBER 15, 2023

PCM not ideal for every drug Continuous manufacturing “may not be fit for every pharmaceutical manufacturing process, but it can bring some advantages in some cases” compared with traditional batch manufacturing, summarized FDA’s Adam Fisher, Ph.D., Vice President and Head - API Process Engineering at Dr. Reddy’s Laboratories.

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European Pharmaceutical Review

SEPTEMBER 29, 2022

The US Food and Drug Administration (FDA)’s Center for Drug Evaluation and Research (CDER) through the Office of Pharmaceutical Quality in 2021 embarked on an initiative to develop a framework for establishing a pharmaceutical manufacturing site quality rating system, the Quality management maturity (QMM) programme.

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Nursing Homes Pharmaceutical Manufacturing Department of Veterans Affairs Dosage 86

Quality Matters

FEBRUARY 9, 2023

However, few companies are developing fully integrated manufacturing capabilities that include drug substance generation and purification, as well as complex drug product manufacturing operations.

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Vaccines Immunity Immunization Labelling 52

epicur

JANUARY 18, 2024

These facilities must comply with the FDA’s stringent cGMP regulations, which ensure a drug has the ingredients and strength stated and is safe for use up to the studied expiration date. BUDs are assigned to these compounded preparations based on the standards established in USP General Chapters (non-sterile) and (sterile).

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Compounding Compounding Pharmacies Dosage Method Validation 52

GMPSOP

AUGUST 28, 2023

Warehouse material handling for pharmaceutical industry Pharmaceuticals quality assurance & validation procedures GMPSOP Warehouse material handling for pharmaceutical industry Prev PREVIOUS POST Table of Contents Warehouse plays a significant role in ensuring pharmaceutical product quality.

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Health and Personal Care Stores Labelling Packaging Documentation 52

Quality Matters

FEBRUARY 13, 2023

Fortunately, the sources of active pharmaceutical ingredient (API) for amoxicillin are geographically diverse, with sources in the U.S., In general, there is a concentration of API manufacturing in India and China for many medicines marketed in the U.S. Europe and India.

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Packaging 52

European Pharmaceutical Review

SEPTEMBER 16, 2022

Since the developed regions of the world started to get COVID-19 under control, focus on this matter has only grown – particularly in the pharmaceutical sector, which played a critical role in curbing the devastation caused by the pandemic. But how will this drive for resilience shape the future of pharmaceutical supply chains?

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Packaging Documentation 95

European Pharmaceutical Review

OCTOBER 31, 2022

Ensuring that small and emerging pharmaceutical companies have access to expertise and resources is especially important. 2 However, smaller companies may have limited in-house resources and lack the capabilities to solve the challenges to meet important milestones during early-stage development.

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Compounding Drug Development Pharmaceutical Companies Pharmaceutical Companies 114

European Pharmaceutical Review

OCTOBER 2, 2023

Eligible companies classified as start-ups and active in the pharma, biopharma, digital, or medical device sectors can exhibit. API Development & Innovation 3. The second panel will be presented by Camille Dumont, Lonza Capsules and Health Ingredients, Juan Colberg, Pfizer, and Sven Stegemann, Leibniz JointLab.

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Packaging 104

Quality Matters

JUNE 21, 2023

The WHO Prequalification (PQ) program also plays a critical role in ensuring that vital health products meet quality standards, including active pharmaceutical ingredients (APIs) and finished drug products. The program helps improve public health in low- and middle-income countries in particular.

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Vaccines 52

GMPSOP

JUNE 16, 2023

Importance of acceptance criteria in analytical method transfer Pharmaceuticals quality assurance & validation procedures GMPSOP Importance of acceptance criteria in analytical method transfer Last modified: June 17, 2023 Table of Contents What is analytical method transfer? QA maintains communication between the laboratories.

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Documentation Dosage Communication Method Validation 52

pharmaphorum

MAY 6, 2022

Sanofi has completed the spin-out of its pharma ingredients business EuroAPI, with shares in the new company rising more than 3% on its starting price of €12 in early trading on the Euronext exchange this morning in a declining market. The post Sanofi ingredients spin-out EuroAPI rises on market debut appeared first on.

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Pharmaceutical Technology

MARCH 22, 2023

In the 1990s, generic pharmaceutical companies in the European Union (EU) offshored the manufacturing of active pharmaceutical ingredients (API) primarily to China. Only 25% of API production for generic drugs took place in Europe in 2020, according to a November 2022 Medicines for Europe report.

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Pharmaceutical Manufacturing Packaging Diabetes Communication 105