Top Stories
At the American Society of Hematology Annual Meeting, Novartis and Kite Pharma both released results from early-phase clinical trials with CAR-T therapies.
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Congress enacted the 21st Century Cures legislation, which shores FDA operations and supports biomedical research at the National Institutes of Health.
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EXPERT INTERVIEW
Rajesh M. Dave, distinguished professor at the New Jersey Institute of Technology, sat down with Pharmaceutical Technology to discuss polymer thin films for drug delivery.
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Industry News
QuintilesIMS forecasts global spending on medicine will reach $1.5 trillion by 2021.
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FDA issued a warning letter to Interquim, SA for CGMP deviations at its Barcelona API facility.
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Supplier News
Through a license agreement with the Broad Institute, Charles River Laboratories will now be offering gene-editing engineering technology.
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Saneca Pharma has received a EUR1.5 million grant from the Slovak Ministry of Education, Science, Research, and Sport, which will be used to drive forward new R&D initiatives for API manufacturing.
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There are 5 different guiding and regulating agencies for cGMP mapping processes. This document summarizes the agencies and the specific articles that should govern your mapping project in warehouses, production facilities, rooms and chambers.
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Spark Therapeutics and Selecta entered a license agreement for Selecta's gene-therapy co-administration technology.
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Connect with top suppliers to the pharma and medical device industry at PACK EXPO East in Philadelphia, February 27 to March 1, 2017. You'll discover new solutions for enhancing safety, security and quality from 400+ exhibitors. Explore 100,000 nsf of packaging innovations and machinery in action. Exchange ideas with 7,000 peers. And gain insights from the Healthcare Packaging and Processing Conference.
 Register today at packexpoeast.com! |
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Regulatory News
Dara Corrigan examines the Mutual Reliance Initiative as a method for expanding FDA's inspection capabilities in Europe and beyond.
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Pharmaceutical Technology's PharmaMarketplace
Your Connection to Global Pharmaceutical Manufacturing Suppliers
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PEER-REVIEWED RESEARCH
Swab recovery parameters are reviewed in detail to define best practices and highlight common mistakes to assure successful recovery studies using a risk-based approach.
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ANALYTICS
Pharmaceutical Technology spoke with Melissa Topp, director of Global Marketing at ICONICS, about the latest in process analytical technology (PAT).
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SCALE-UP/TECH TRANSFER
The success of a pharmaceutical manufacturing transfer from one facility to another requires detailed operational plans, attention to detail, and coordination between all parties.
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Events
January 9–13, 2017
February 1–2, 2017
May 16–18, 2017
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REFERENCE BOOKS |
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Increase your knowledge of solid dosage technology and solid dose tablet manufacturing processes. These comprehensive pharmacology reference guides cover a variety of solid-dosage form principles such as oral solid-dosage forms, powders, mixing and blending, excipients, tableting, and coating. Drug delivery system manufacturing professionals can use the solid dosage manufacturing books to stay current with compressed tablet manufacturing processes, solid dosage processing equipment, tablet-pressing processes, and pharmaceutical industry trends in oral solid dosage manufacturing and solid dosage form development.
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eBOOKS
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Quality issues can appear at any stage of the bio/pharmaceutical development and manufacturing supply chain. Drug companies must monitor raw materials, suppliers, contract service providers, facilities, manufacturing processes, and production workers. In this e-book, the editors examine current quality issues, and how the industry is addressing quality challenges throughout the supply chain. |
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