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Pharmacovigilance of Vaccines in the USA (US FDA)
Pharmacovigilance is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or...
Aug 30, 20244 min read
US FDA Pharmacovigilance Requirements for Drugs in the USA
Pharmacovigilance is a cornerstone of drug regulation in the USA, playing a crucial role in ensuring the safety and efficacy of medicinal...
Aug 13, 20244 min read
Microbiome Based Therapies : Regulations and Market Outlook
Microbiome-based therapies are a promising area in precision medicine, aiming to tailor treatments based on individual microbial...
Aug 7, 20246 min read
US FDA Regulation of Nitrosamines in the USA
Nitrosamines are a class of compounds known for their potent carcinogenic effects. Their discovery in pharmaceuticals has sparked...
Jul 26, 20245 min read
Biopharmaceutical Alliance Launched by India, South Korea, US, Japan, and EU
The global biopharmaceutical sector has taken a significant step towards ensuring a resilient drug supply chain with the formation of the...
Jun 7, 20243 min read
Case Study: Nitrosamine Impurities Analysis - Artixio’s Strategic Staffing Solutions for a Generic Drug Manufacturer based in the USA
Artixio helped a US based Generic Drug Manufactur with Nitrosamine Impurities Analysis through Strategic Staffing Solutions
Apr 2, 20242 min read
FAQs - Modernization of Cosmetics Regulation Act of 2022 (MoCRA)
The Modernization of Cosmetics Regulation Act 2022 (MoCRA) was signed into law at the end of 2022
Feb 20, 20243 min read
US FDA Guidance on Registration and Listing of Cosmetic Products and Facilities under Modernization of Cosmetics Regulation Act (MoCRA)
In December 2023, the United States Food and Drug Administration (FDA) ushered in a new era for the cosmetics industry with the release...
Jan 1, 20245 min read
US FDA’s final guidance on Digital Health Technologies for Clinical Investigations
The landscape of clinical investigations is evolving rapidly with the integration of Digital Health Technologies (DHTs). The US FDA has...
Dec 28, 20235 min read
US FDA Modernization of Cosmetics Regulation Act of 2022 (MoCRA)
The Modernization of Cosmetics Regulation Act (MoCRA), which was signed into law on December 29, 2022, is a significant milestone in the...
Oct 29, 20235 min read
The Q-Submission Meetings for Medical Devices with US FDA
The US Food and Drug Administration (US FDA) Q-Submission Program serves as a vital channel for medical device manufacturers to engage...
Oct 23, 20236 min read
US FDA RFD and Pre-RFD Submissions for Combination Products in USA
The healthcare landscape is in a perpetual state of transformation, and as a consequence, there is a noticeable surge in the development...
Oct 20, 20234 min read
Medical Device Registration in USA : 510(k) Registration with US FDA
In the realm of medical devices, regulatory compliance is paramount to ensure patient safety and effective product performance. The...
Oct 11, 20234 min read
Medical Device Registration in USA by US Food and Drug Administration (US FDA)
Medical Devices Regulatory Overview in USA The responsibility for overseeing the regulations of medical device companies involved in the...
Oct 7, 20236 min read
The US Agent: Your Essential Partner for FDA Regulatory Success
The United States Food and Drug Administration (FDA) plays a pivotal role in ensuring the safety and effectiveness of medical devices,...
Oct 4, 20236 min read
Biologics and Biosimilars Regulations, Registration Process in the USA (FDA)
The size of the U.S. biosimilars market, estimated at USD 6.73 billion in 2021, is expected to increase by USD 9.48 billion in 2022 and...
Aug 9, 20235 min read
Expanded Access by USA FDA for Investigational Drugs
In the United States, the approval process for unregistered medicinal products under Early Access Program (EAP) is known as Expanded Access
Jun 20, 20232 min read
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Deep dive and engage in insightful discourse driven by concurrent global regulatory scenarios, industry trends and Artixio’s real-time experience across the product value chain. Whitepapers, research articles, landscape reports and case studies to help you stay ahead of the curve.
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