European Pharmaceutical Review

MAY 28, 2024

This can raise safety concerns for patients, due to important information not being present on the packaging, the report stated. The region’s “efficient production, distribution, and administration of pharmaceutical products” is also pushing the demand for this packaging.

Marketing 72

Marketing Transportation Distribution Pharmaceutical products 72

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 88

Medicine Food and Drug Administration Pharmaceutical products Pharmaceutical 88

European Pharmaceutical Review

DECEMBER 19, 2023

However, this greatly complicates both the worldwide distribution and stockpiling of vaccines and other drugs. This requires the development of technologies to rapidly produce effective, safe, stable vaccines that can be manufactured and distributed quickly. Injection Safety Fact Sheet. at 100°C for 24 hours. Internet] WHO.

Distribution 96

Distribution Manufacturing Food Specialization 96

Contrarian Sales Techniques

DECEMBER 4, 2023

For starters, it's about customization to suit the specific nature of pharmaceutical products. Temperature Control: Keeping Samples Safe For certain pharmaceutical products, maintaining a specific temperature range is essential. This feature is vital to maintain the integrity of certain pharmaceutical products.

Sales 52

Sales Pharmaceutical Sales Pharma Ethics 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.

Leads 52

Leads Marketing Pharmaceutical Pharmaceutical manufacturing 52

European Pharmaceutical Review

MARCH 12, 2024

Regulatory bodies such as the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) place great importance on data integrity in the pharmaceutical/life science industry. What is the main recommendation you would make to the pharmaceutical/life science industry to ensure a strong data governance framework?

Government 85

Government Pharma Ethics Training 85

European Pharmaceutical Review

JANUARY 16, 2023

Cellular products directed towards personalised medicine have short manufacturing cycles, small batch sizes, demanding analytical methods, and short shelf lives. The US federal drug GMP regulations that first became official in 1977 and their European counterparts will need to be re-interpreted for this new generation of products.

Pharmaceutical 124

Pharmaceutical Food and Drug Administration Manufacturing FDA 124