Accumulation: Understanding Its Significance and Methods for Calculation Accumulation Michael requested a discussion on the concept of accumulation, a term commonly encountered in both nonclinical and clinical contexts. While some individuals approach this term...
News Articles / Regulatory affairs
by samitfm · Published April 4, 2024 · Last modified January 9, 2025
Shrimp exporters adhere to strict regulations for safety and aim for Rs 1 lakh crore in exports, according to officials. shrimp exporters Indian are placing a significant emphasis on ensuring the quality and safety of...
News Articles / Pharmaceutical engineering
by samitfm · Published March 29, 2024 · Last modified January 9, 2025
What & How (AI) Artificial-Intelligence used in medicine (Pharmaceuticals)in 2024 Artificial-intelligence: What is (AI) artificial intelligence in medicine in 2024. Artificial intelligence (AI) in medicine refers to the use of advanced computational techniques to...
News Articles / Regulatory affairs
by samitfm · Published March 29, 2024 · Last modified December 30, 2024
Amazing application of artificial intelligence (AI) in the 2024 pharmaceutical industries Amazing application of artificial intelligence in pharma, throughout our journey, humanity has traversed a vast terrain in pursuit of understanding AI. Since the...
News Articles / Regulatory affairs
by samitfm · Published March 29, 2024 · Last modified January 9, 2025
what are drugs designed by AI
Clinical Research / News Articles
by samitfm · Published March 14, 2024 · Last modified January 9, 2025
What is Bioavailability and Bioequivalence Study? What is Bioavailability and Bioequivalence Study? Bioavailability refers to the proportion of a drug from a given dose that enters the bloodstream and the speed at which it...
Estimate of pharmacokinetic parameters. From non-Compartmental data using -Microsoft Excel-24 Estimate of pharmacokinetic parameters (CDISC) using Microsoft Excel-estimation , Pharmacokinetic parameters, such as clearance (CL) and volume of distribution (V), represent constants that vary...
Overview of statistical concepts-Bioequivalence Pharmacokinetics INTRODUCTION Overview-of-statistical-concepts-bioequivalence, Current global regulatory agencies mandate that the final assessment of an oral medication\’s quality relies on its in vitro dissolution behavior, along with in vivo bioavailability and/or...
News Articles / Regulatory affairs
by samitfm · Published March 4, 2024 · Last modified January 10, 2025
What is Drug products approval System Regulatory affairs in 2024 Authorization in drug products Drug products approval system Regulatory affairs, A medicinal product, whether intended for human or veterinary use, must obtain a valid...
News Articles / Regulatory affairs
by samitfm · Published March 2, 2024 · Last modified January 10, 2025
How eCTD 4.0 implementation in Regulatory Affairs eCTD 4.0 – The electronic Common Technical Document (eCTD) is standardized guideline for submitting regulatory information to health authorities (HAs). It streamlines the process of electronically implementing...
Follow:
At Zaims Pharma, we focus on the intersection of pharmaceutical regulations, compliance standards, and the transformative power of technology. Our team is passionate about simplifying the complexities of the industry, whether through in-depth articles, expert interviews, regulatory updates, or software solution reviews. We provide valuable tools and actionable insights that help our readers navigate the evolving landscape of pharmaceuticals and healthcare.
Zaims Pharma’s content is for informational and educational purposes only. Our website is not intended to be a substitute for professional medical advice, diagnosis, or treatment.
More
Recent Comments