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Webcasts:

SGS Webcast Series: What's New in Pharmaceutical Laboratory Testing Requirements?
Monday, June 14, 2010
10:00 AM ET(New York); 4:00 PM CET (Paris)
SGS Webcast Series Part 1: Heavy Metals
This webinar will highlight the changes affecting industry in the area of heavy metals testing, including a look at the latest US Pharmacopeial revisions (<231> Heavy Metals) and replacement chapters (<232 Elemental Impurities-Limits><233 Elemental Impurities-Procedures><2332 Contaminants in Dietary Supplements> as well asdifferences in impurity testing between the global pharmaceopeias USP, JP, and Ph.Eur.

» Register Free Today!
Sponsored by: SGS

Tuesday, June 22, 2010
2:00 PM ET
SGS Webcast Series Part 2: Extractables and Leachables
Monomers and additives such as antioxidants, plasticizers, and stabilizers may potentially migrate into medicinal products and should be evaluated as required by regulatory authorities. Processing equipment as well as primary and secondary container materials must be considered. This webinar will highlight the changes affecting industry in the area of extractables and leachables testing, including a look at implementing ICH Q4B and global pharmacopeial differences between USP, JP, and Ph.Eur. requirements.

» Register Free Today!
Sponsored by: SGS

Tuesday, June 29, 2010
2:00 PM ET
SGS Webcast Series Part 3: Melamine and Contamination Challenges
This webinar will highlight the changes affecting industry in the area of melamine testing and related contamination issues, including recent FDA guidance, USP monographs, and international harmonization efforts.

» Register Free Today!
Sponsored by: SGS

Wednesday, June 23, 2010
11:00 AM ET
What Early Stage Companies Need to Know About Quality Management: Lessons Learned from Industry Leaders
What Early Stage Companies Need to Know About Quality Management: Lessons Learned from Industry Leaders Live Event Date/Time: June 23, 2010 at 11:00 AM EDT Life sciences companies are trying to cope with the mounting challenges of managing and maintaining quality systems while facing increased compliance risks. Clinical trials are becoming more complex and the FDA is scrutinizing data to a higher degree. This is leading to increased demands on quality organizations, and many are drowning in paper-based systems while struggling to maintain compliance. A panel of industry professionals will share, through a facilitated discussion, their experiences with deploying and realizing the benefits of QMS. They will discuss best practices they have implemented and lessons they have learned.

» Register Free Today!
Sponsored by: Sparta Systems

OnDemand
Topical Formulation Development and Screening
In this webcast we will help you understand the routes for drug penetration into human skin and the factors which dictate the penetration potential of a drug. You will learn about in vitro skin penetration models of normal and diseased skin for use in screening topical formulations.

» Register Free Today!

Featured Podcasts:

Expansion of Vetter Development Service (VDS)
The North American market is critical to Vetter's strategic global growth as nearly half of its client base is already located here. In order to maximize on this opportunity, Vetter has decided to create a facility, its first outside of Germany, at the Illinois Science + Technology Park in suburban Chicago. The facility, which supports preclinical to phase II clinical batch projects, is an expansion of Vetter Development Service. With significant progress already having been made, the facility is scheduled to be operational by beginning of the fourth quarter 2010.

» Listen


Pfizer's Maddaluna on Integrating Wyeth's Manufacturing Organization

Join Michelle Hoffman, Editor in Chief of Pharmaceutical Technology and Marina Aslanyan, Vice Solutions Delivery & Customer Care, Sparta Systems, Inc. as they discuss what contributes to a successful quality system implementation. Listen in and hear tips and tricks that will help make your quality management deployment a success.
» Listen  

Featured Videos:

Operations Excellence Through Quality Management Software
Listen to Sparta Systems Industry Principal, Tim Mohn, discuss pressing issues that companies in the life science industry face. Ranging from the changing landscape of healthcare reform, to the expected ROI life science companies demand, Tim explores the benefits enterprise quality management software can deliver to help streamline processes and ensure quality and compliance across the supply chain.

» View Video
Sponsored by: Sparta Systems

 


 
Using Innovation to Unlock and Extend Value
Clive Bennett discusses how customers are looking for ways to extract more value from existing chemical entities and how they’re using 505-B2 filings as a way to extend the lifecycle of molecules. Halo Pharma offers innovative approaches to lifecycle management through its comprehensive development and manufacturing services and has a particular expertise with 505-B2 filings.

» View Video
Sponsored by: Halo Pharma

Featured Whitepapers:

Maximizing Value of Mature Products
Pillar5 Pharma Inc. has emerged as a new entry in the contract manufacturing arena. They are a relatively small Canadian based company, manufacturing for Canadian and global markets from a former Pfizer facility in Arnprior, Ontario.

» View Whitepaper
Sponsored by: Pillar5 Pharma Inc.


Donning by Design

This paper addresses the importance of process protection in cleanrooms via the appropriate cleanroom suit. It provides an overview of the sterile cleanroom apparel category and defines key areas for improvement. It introduces a new concept for sterile cleanroom gowning to help minimize the problems associated with current technologies.
» View Whitepaper

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