Remove 2020 Remove Compounding Remove Pharmaceutical Manufacturing
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NHC Submits Comments on Section 232 National Security Investigation of Imports of Pharmaceuticals and Pharmaceutical Ingredients

Putting Patients First Blog

4 ,5 Millions of Americans rely on medicines that are manufactured outside the United States, particularly from close and longstanding allies such as Ireland, Switzerland, and the United Kingdomcountries whose regulatory frameworks for pharmaceutical manufacturing mirror the high standards enforced domestically.

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Pharmacy Policy Updates for June 2025

Pharmacy Times

The first one was introduced on September 13, 2020, near the end of Trump’s first term, but was shut down by a federal judge due to the administration’s failure to comply with the proper implementation processes. September 13, 2020. Trump to pitch sweeping Medicare drug price plan. May 7, 2025. Accessed May 13, 2025.

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Building CO2-neutral, defossilised supply chains for chemicals

European Pharmaceutical Review

2 However, most of these efforts relating to catalysis, 3 process waste metrics, 4 lifecycle assessments, 5 pharmaceuticals in the environment 6 and the phase out of substances of concern 7 mainly mitigate the consequences of pharmaceutical manufacturing. Gene Ther 27, 537–544 (2020). Science 369, eabc3183 (2020).

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Pharma Microbiology East Coast Conference – A Virtual Conference with Remote Access

pharmaphorum

SMi Reports: SMi Group have made the decision due to travel restrictions to open the conference and workshops to all microbiologists by transforming it into a virtual-remote online access event only on October 28 and 29 2020. SMi’s 3rd Annual Pharmaceutical Microbiology Conference will no longer take place in Boston. SMiPharmaMicroEC.

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The Pandemic Treaty and the opportunity to end ‘vaccine apartheid’

pharmaphorum

The world was caught unprepared for the global pandemic that struck in 2020. Compounding the situation to understand how such an outcome was allowed to occur is the fact that many deals between government and pharmaceutical companies selling the treatments and vaccines were agreed under terms of confidentiality.

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Ensuring Product Safety: U.S. FDA Guidance on Testing High-Risk Drug Components for Diethylene Glycol and Ethylene Glycol

Quality Matters

The manufacturer must perform test B “Limit of Diethylene Glycol and Ethylene Glycol” to check whether DEG and EG content is no more than 0.10 % prior to use, and not use it if the level is higher than 0.10 %. Regulatory agencies in different countries can use the U.S.