Eli Lilly, a key player in the pharmaceutical industry, is taking a stand against counterfeit medications. The company has initiated legal action against
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In the pharmaceutical industry, analytical development plays a pivotal role in ensuring the safety, efficacy, and quality of drugs. This intricate field involves the application of various scientific disciplines, including chemistry, biology, and physics, to analyze drug components and products throughout the development process. As pharmaceutical companies strive to meet rigorous regulatory standards and cater […]
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Pharmaceutical Analytical Testing Market is growing at a CAGR of 8.7% over the next 7 years. SGS SA, Labcorp, Eurofins Scientific, Pace Analytical Services LLC, Intertek Group plc, PPD Inc . and many more major companies operating in this Market.
M.Sc in Pharmacovigilance & Clinical Research: This postgraduate program lays special emphasis on providing expertise in the evaluation of medicines
The pharmaceutical industry stands at the forefront of scientific innovation, dedicated to developing life-saving drugs and treatments. Ensuring the efficacy and safety of pharmaceutical products is a critical responsibility. One indispensable tool in this quest is the walk-in test chamber. In this article, we will explore the vital role of walk-in test chambers in the […]
The pharmaceutical industry is expected to be worth $1.5 trillion by 2023, and the field of pharmacovigilance plays a crucial role in ensuring the safety of drugs. Artificial Intelligence (AI) and Machine Learning (ML) models are being applied to improve the pharmacovigilance process, including case intake using Optical Character Recognition (OCR) and Natural Language Processing (NLP), natural language generation (NLG) for narrative writing, robotic process automation (RPA) for dynamic case workflow, AI-based signal detection, and AI-based adverse event prediction. These advancements have the potential to increase efficiency, accuracy, and consistency in pharmacovigilance, as well as reduce costs and delivery timelines for pharmaceutical organizations.
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Introduction: The Importance of Clinical Research in the Pharmaceutical Industry Clinical research is a critical component of the drug development process in the pharmaceutical industry. It involves t...
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Pharmaceutical Analytical Testing Market In recent years, the importance of pharmaceutical analytical testing has been steadily rising, beco...
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Pregnancy and the Pharmaceutical Industry: The Movement Toward Evidence-based Care for Pregnant Women explores the issues surrounding the decision to undertake clinical trials with pregnant women. There is currently a lack of data on the safety and effectiveness of medications used during pregnancy as it is impossible to extrapolate that information from drug studies on men and non-pregnant women. As a majority of pregnant women confront a medical condition during their pregnancy, from simple pain, to ongoing or new medical issues, this book quantifies the current absence of pregnant women in drug studies and identifies ethical issues, barriers, litigation fears and opportunities. Those in the pharmaceutical industry, IRB members who approve or deny drug study plans, doctors, nurses and midwives working in obstetrics or involved in conducting studies at their institutions will find this book an essential resource. Explores the medical, ethical, scientific and legal rationales behind the inclusion of pregnant women in drug studies Describes how pharma and biotech companies can safely implement the new FDA guidance and begin to include pregnant women in drug testing Shares views from pharmaceutical industry insiders about company risks, reluctance to implement guidance, and the ultimate need to include pregnant women in studies | Author: Kristine E. Shields | Publisher: Academic Press | Publication Date: May 24, 2019 | Number of Pages: 244 pages | Language: English | Binding: Paperback | ISBN-10: 0128185503 | ISBN-13: 9780128185506
The professional figures that move within Regulatory Affairs are mainly concerned with supervising the authorization procedures for the marketing of the
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In the pharmaceutical industry, ensuring the quality, safety, and efficacy of medicines is paramount. Good Manufacturing Practice (GMP) Certification plays a pivotal role in this endeavor, providing…
Mathematical and Statistical Skills in the Biopharmaceutical Industry: A Pragmatic Approach describes a philosophy of efficient problem solving showcased using examples pertinent to the biostatistics function in clinical drug development. It was written to share a quintessence of the authors' experiences acquired during many years of relevant work in the biopharmaceutical industry. The book will be useful will be useful for biopharmaceutical industry statisticians at different seniority levels and for graduate students who consider a biostatistics-related career in this industry. Features: Describes a system of principles for pragmatic problem solving in clinical drug development. Discusses differences in the work of a biostatistician in small pharma and big pharma. Explains the importance/relevance of statistical programming and data management for biostatistics and necessity for integration on various levels. Describes some useful statistical background that can be capitalized upon in the drug development enterprise. Explains some hot topics and current trends in biostatistics in simple, non-technical terms. Discusses incompleteness of any system of standard operating procedures, rules and regulations. Provides a classification of scoring systems and proposes a novel approach for evaluation of the safety outcome for a completed randomized clinical trial. Presents applications of the problem solving philosophy in a highly problematic transfusion field where many investigational compounds have failed. Discusses realistic planning of open-ended projects.
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First published in 1984, this book examines corporate crime in the pharmaceutical industry and is based on extensive research, including interviews with 131 senior executives of international pharmaceutical companies. It covers topics such as international bribery and corruption, fraud in the testing of drugs and criminal negligence in the unsafe manufacturing of drugs. | Author: John Braithwaite | Publisher: Routledge | Publication Date: May 14, 2014 | Number of Pages: 450 pages | Language: English | Binding: Paperback | ISBN-10: 0415815649 | ISBN-13: 9780415815642
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The pharmaceutical industry and drug regulators face numerous challenges in pharmacovigilance, patient safety, and addressing areas of unmet medical needs in an environment where development costs have increased exponentially while filings and launches have decreased significantly.
