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Podcasts

Engineering Solutions to Solve Challenges in Pharmaceutical Processing: Powder Handling
Live Webcast On: Wednesday, September 11, 2013 at 11:00 AM EDT
Sponsored by: Patheon

Minimizing Out-of-Specification (OOS) Errors Using a Risk-based Gravimetric Approach
On Demand
Sponsored by: Mettler Toledo

New Strategies for Evaluating BioPharmaceutical Stability
On Demand
Sponsored by: ABC Labs

More Webcasts

Events

Validation Week
Oct. 22-24, 2013
San Diego, CA USA

Manufacturing Execution Systems Conference
Aug. 13-14, 2013
Philadelphia, PA USA

Cleaning Validation and Critical Cleaning Processes
Aug. 19-21, 2013
Philadelphia, PA USA

Qualifying and Validating Cloud Computing
Aug. 20-21, 2013
San Diego, CA

More events


Advertisement:
Engineering Solutions to Solve Challenges in Pharmaceutical Processing: Powder Handling
Live Webcast: Wednesday, September 11 at 11:00 am EDT.
Click here to Register Free.

Podcasts
Advertisement:
Pharmaceutical Technology presents its Analytical Testing Resource Guide combo
A compilation of articles in a three-handbook set covering general Analytical Testing and Stability in the manufacture, packaging, storing, and testing of formulated products. ... Click here

August 8, 2013 PharmTech.com PRINT SUBSCRIBE DIGITAL SUBSCRIBE


News

Court Ruling Threatens Drug Shortage Remedy
The Food and Drug Administration may no longer be able to alleviate shortages in vital drugs by permitting the import of unapproved medicines.
Click Here to Read More

Advertisement:
Life Sciences Guidebook: Best Practices for FDA Compliance Solutions
This guidebook provides you with a basic overview for selecting, implementing and using FDA Compliance and Quality Management solutions. Learn the importance of QMS, best practices for FDA Compliance and Quality systems, and tips and tricks for finding the solution best suited for your company. Read More

FDA Publishes Generic-Drug User Fees
FDA has published the required generic-drug user fees for fiscal year (FY) 2014.
Click Here to Read More

Advertisement:
1-Hour Webinar: The Basics of Validation
This webinar covers the basics of validation, including regulations that mandate it. Here's what webinar attendees said:

"Vaisala’s webinars are wonderful [if you're] trying to learn as much as possible about this field…"Danielle, Validation/Calibration Technician

"This knowledge can be applied to real-world applications immediately ..."Pat, Technical Specialist – Calibration

Watch this Recorded Webinar...

EMA Reorganizes
The European Medicines Agency is moving forward with plans to restructure the organization.
Click Here to Read More

Advertisement:
Get Your Equipment CLEANER, FASTER!
Clean, rinse and dry your manufacturing equipment in minutes! Your cleaning process doesn’t have to be a hassle — get a more thorough cleaning in 3 easy steps. Learn More!

Nearly 450 Medicines in Development For Neurological Disorders
America’s biopharmaceutical research companies are developing 444 new medicines to prevent and treat neurological disorders, according to a new report released by PhRMA.
Click Here to Read More

Advertisement:
Nearly 100 global pharmas and consumer healthcare organizations partner with Ropack for contract manufacturing and packaging services. Focused on quality and reliability, Ropack provides bottling, blisters in multiple formats and pouch/sachet filling. Now Ropack also offers stick-pack filling of temperature- and humidity-sensitive products in a controlled environment.  Stick-pack, particularly for pediatric applications, is ideal for reformulation and patent protection. (513) 846-0921; [email protected]
Live Link: Ropack.com

Emerging Pharma Leaders Tapped by Pharmaceutical Executive Magazine
Selected trendsetters reflect changes in the pharmaceutical industry.
Click Here to Read More

Advertisement:
Safe Automated Weighing of Potent Compounds in the Pharmaceutical Industry
Agilent partners with Pharma for great results. Download or request a hard copy of our new guide, Genotoxic Impurities in Pharmaceutical Products:  Regulations and Analysis, authored by Ludwig Huber. The guide provides specific guidelines for genotoxic impurities and recommendations for implementation according to EMA and FDA guidelines.
Get your copy now

Donaldson Expands Lab at Minnesota Headquarters
Donaldson Company, Inc. announced a $10 million expansion of its testing laboratories at its Bloomington, Minn., corporate headquarters.
Click Here to Read More

Metrics Names Wes Edwards Chief Financial Officer
Edwards will oversee company’s financial, logistical, and human-resources operations.
Click Here to Read More

Thermo Fisher Scientific Opens Dry Powder Media Facility in Singapore
Singapore facility delivers manufacturing redundancy and increases supply assurance for global biologic drug discovery and production.
Click Here to Read More

SBRI Healthcare Awards Funding for Phase 2 Development Program
Funding awarded to develop innovative solutions that address unmet health needs.
Click Here to Read More

Novel Drug Shuts Down Master Protein Key to Lymphoma
Weill Cornell scientists reveal how a protein drug eradicated human lymphoma in mice.
Click Here to Read More



News

Drug Delivery Insights: Strategies for Solubility and Bioavailability Enhancement of Poorly Soluble Drugs
Kurt Nielsen, PhD, chief technology officer and senior vice-president of R&D at Catalent Pharma Solutions, discusses strategies for solubility and bioavailability enhancement of poorly water-soluble drugs.
Click Here to Read More

Q&A with Claudia Roth, President, Vetter Development Service, USA
Claudia Roth, President of Vetter Development Service USA, discusses trends in single-use technology for clinical manufacturing.
Click Here to Read More

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Podcasts

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Advertisement:
Achieving GMP Compliance for Environmental Monitoring Systems
Live Webcast: Wednesday, August 21, 2013 at 1:00 PM EDT.
Click here to Register Free.
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