Pharmaceutical Technology - Pharmaceutical Manufacturing & Development News & Research for Scientists

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PharmTech

Latest Issue
PharmTech Europe

Solving Poor Solubility with Amorphous Solid Dispersions
Weighing the pros and cons of hot-melt extrusion and spray drying.
Analytical Method Comparability in Registration and Post-Approval Stages: A Risk-Based Approach
A risk-based approach is recommended for analytical method comparability for HPLC assay and impurities methods.
New Technologies Enhance the Formulation of Highly Potent Drugs
Advances in solid and liquid formulation techniques are providing more options.
The Role of Normal Data Distribution in Pharmaceutical Development and Manufacturing
Review challenges in the use of normality testing situations and recommendations on how to assess data distributions in the pharmaceutical development manufacturing environment
Fluorination Remains Key Challenge in API Synthesis
Safer fluorinating reagents and access to GMP fluorination capabilities remain challenges in API synthesis.
Marrying Big Data with Personalized Medicine
Data analytic strategies can help companies capitalize on personalized medicine.
PharmTech eBook Series
Bioprocessing and Sterile Manufacturing
Review emerging trends in the development and manufacturing of parenteral and biologic drugs, including continuous manufacturing, monitoring, sterilization procedures, modular manufacturing, and single-use technologies.
Solid Dosage and Excipients
Review emerging trends in the formulation and manufacture of solid dosage drugs, as well as the role of excipients in enhancing the functionality of these drug forms.

Expert Interviews, Industry Trends, and more

USP Supply Chain Safety Videos
Peer-Reviewed Articles
The Role of Normal Data Distribution in Pharmaceutical Development and Manufacturing
Investigation of Various Impurities in Febuxostat
Comparing Manufacturing Process Options
Cleanability of Pharmaceutical Soils from Different Materials of Construction
Achieving Zero-Order Release Kinetics Using Multi-Step Diffusion-Based Drug Delivery
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FDA Reorganization to Promote Drug Quality
FDA Readies Quality Metrics Measures
New FDA Team to Spur Modern Drug Manufacturing
From Generics to Supergenerics
CMOs and the Track-and-Trace Race: Are You Engaged Yet?
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Industry Leaders: Q+A
Q&A with Paul Nelles, Vetter Development Service
Paul Nelles of Vetter Development Service discusses prefilled syringes.

PharmTech Europe 25th Anniversary
Tracking the Pulse of the Pharmaceutical Industry
Pharmaceutical Technology Europe marks its 25th anniversary.
Standards & Regulations
Hospira Recalls Certain Lots of Intravenous Products
Hospira voluntary recalls certain lots of several LifeCare products due to potential for leakage.
EMA Releases Pharmacovigilance Meeting Highlights
The European Medicines Agency releases highlights from its Pharmacovigilance Risk Assessment Committee safety review meeting in October.
FDA Releases Guidance on Critical Path Innovation Meetings
FDA outlines procedures for having a Critical Path Innovation Meeting with CDER.
FDA Releases Q&A on DQSA
FDA releases question and answer draft guidance on drug product tracing and licensing requirements.
Jim Miller Outsourcing Outlook Jim MillerCMO Industry Thins Out
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerFluorination Remains Key Challenge in API Synthesis
Marilyn E. Morris Guest EditorialMarilyn E. MorrisBolstering Graduate Education and Research Programs
Jill Wechsler Regulatory Watch Jill Wechsler Biopharma Manufacturers Respond to Ebola Crisis
Sean Milmo European Regulatory WatchSean MilmoHarmonizing Marketing Approval of Generic Drugs in Europe
EVENTS
Oct 22, 2014 - Oct 23, 2014
Single-Use Systems for Manufacturing of Parenteral Products
Oct 28, 2014 - Oct 30, 2014
20th Annual Validation Week
Oct 28, 2014 - Oct 30, 2014
Validation of Biotechnology-related Cleaning Processes
Nov 2, 2014 - Nov 6, 2014
AAPS Annual Meeting 2014
Nov 2, 2014 - Nov 5, 2014
Pharma Expo
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