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Podcasts

Best Practices for Effective Environmental Monitoring Program in Bio/Pharmaceutical Production
Tuesday, April 22, 2014 at 11 AM-Noon EST
Tuesday, April 29, 2014 at 10:00-11:00 AM CET
Sponsored by: SGS Life Science Services

Life Cycle Management Opportunities In Softgel Technologies: Regulatory and Technological Aspects
Wednesday, May 21, 2014 at 11:00 AM EDT
Sponsored by: Patheon

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

More Webcasts

 
Events

15th Annual Computer and Software Validation Forum
April. 23-25, 2014
San Diego, CA USA

ISPE Europe Annual Conference 2014
April. 28-30, 2014
Frankfurt, Germany

Respiratory Drug Delivery (RDD) USA 2014
May 4-8, 2014
Fajardo, Puerto Rico

Interpack 2014
May 8-14, 2014
Dusseldorf, Germany

More events



April 10, 2014 PharmTech.com PRINT SUBSCRIBE DIGITAL SUBSCRIBE


News

A New Approach to Forced Degradation Studies Using Anhydrous Conditions
In this article, the authors demonstrate that a normal-phase chromatographic method was stability-indicating for a water-sensitive prodrug. The stress conditions using aqueous and non-aqueous conditions were also compared to understand the information obtained with each approach.
Click Here to Read More

Best Practices in Adopting Single-Use Systems
Bioprocessors should understand the key factors associated with implementing single-use components or platforms, which include materials of construction, components, system design, and vendor support.
Click Here to Read More

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Performance Qualification Protocols
What’s the quickest solution to a robust PQ of your environmental monitoring system: DIY or vendor supplied? This article discusses the keys to evaluating “canned” PQ documents from suppliers and options for creating your own protocols. Also, is skipping the PQ process an option?Learn more.

Separation of Compliance and Performance Under FDASIA
The root cause of drug shortages is mismanagement of variation.
Click Here to Read More

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Complimentary White Paper: The Benefits of Implementing FDA's eMDR Program
The FDA has taken the next step in increasing efficiency of electronic regulatory reporting through the implementation of the electronic Medical Device Reporting (eMDR) initiative. Learn the benefits and best practices of implementing FDA's eMDR program to increase reporting efficiency and reliability within your Life Science organization.Download Now

FDA Wants You!
A number of top management positions at the Center for Drug Evaluation and Research (CDER) need to be filled, and CDER leaders are looking for experienced industry managers to help rebuild its staff.
Click Here to Read More

News

Takeda, Lilly to Challenge $9 Billion Verdict in Diabetes Drug Case
Takeda Pharmaceuticals and Eli Lilly announced that they plan to challenge a $9 billion judgment in a lawsuit that alleged Actos caused bladder cancer.
Click Here to Read More

Advertisement:
Natoli Engineering Company is an industry leader and expert in manufacturing tablet compression tooling including multi-tip, single tip, micro-tab, exotic shapes, die table segments and more, from various high-quality steels and specialty coatings. In addition to presses, tooling, and machine parts, Natoli offers a comprehensive tableting accessories catalog. We also provide training seminars and tablet press refurbishing. Scientific and Metallurgy divisions offer additional specialized services.www.natoli.com

Sun Pharma to Acquire Ranbaxy
Sun Pharma acquisition of Ranbaxy Laboratories will create the fifth-largest specialty generics company in the world.
Click Here to Read More

Advertisement:
Ever consider Single–Use Sensors in your mixing?
Flexel® for LevMixer® Magnetic Mixer with pre-assembled pH sensor and thermowell is an innovative single-use solution providing ultra-clean and high-torque agitation, with in-line pH and temperature monitoring from 50L to 1,000L.
Ideal for:
  • Dilution prior to chromatography
  • Low pH virus inactivation
  • pH adjustment of column eluate
  • Protein re-folding
  • Product formulation
Sartorius Stedim Biotech design, manufacture and sterilization processes are conducted under conditions that meet cGMP requirements.
Learn more

EDQM Launches Counterfeit Drug Database
EDQM has launched a database, Know-X, which collates reports on counterfeit/falsified medical products that have been detected in Council of Europe member states.
Click Here to Read More

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Navigating the Analytical Development Challenges for Bioprocess Residuals and Impurities
On Demand Webcast
To Register free: www.pharmtech.com/navigating

A New Plant Biotech Approach for Efficient Production of Pharmaceutical Compound
European scientists have discovered a method to improve the efficiency of the pharmaceutical production through plant biotechnology.
Click Here to Read More

FDA Approves Auto-Injector to Reverse Opioid Overdose
Evzio, the first naloxone treatment specifically designed to administered to opioid overdose patients by family members or caregivers, approved in 15 weeks.
Click Here to Read More


News

Merck Announces Management Changes
Merck promotes internal managers to head Merck Millipore and Consumer Health Divisions.
Click Here to Read More

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Overcoming Challenges in the Development of Active Drug-Layered Formulations for Multiple Dosage Forms
On Demand Webcast
To Register free: www.pharmtech.com/overcomingchallenges

ChemCon Passes its Fourth FDA Inspection
ChemCon passes its fourth FDA inspection in the 17-year history of the company.
Click Here to Read More

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Best Practices for Effective Environmental Monitoring Program in Bio/Pharmaceutical Productions
US: Tuesday, April 22 at 11:00 am EDT | EU: Tuesday, April 29 at 10:00 am CET
To Register free: www.pharmtech.com/emp

Carolina Medical Products Renamed CMP Pharma
Carolina Medical Products changes its name to CMP Pharma to reflect current business trends.
Click Here to Read More

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Life Cycle Management Opportunities in Softgel Technologies
Live Webinar:Wednesday, May 21, 2014 at 8:00am PDT/ 10:00am CDT/11:00am EDT
To Register Free: www.pharmtech.com/opportunities.

Dalton Pharma Completes Aseptic Filling Capabilities Expansion
Dalton Pharma completes its $2.5 million expansion in Toronto for sterile and aseptic filling capabilities.
Click Here to Read More


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Events
Analytical and Bioanalytical Testing
Review case-study analyses of the chromatographic, spectroscopic, and imaging methods used in the identification, characterization, and qualification of drug substances and drug products as well as impurity analysis.Download Now

Podcasts
Advertisement:
Pharmaceutical Technology presents its Process Analytical Technology resource guide combo
A compilation of informative, useful articles designed to help you meet the challenges of process analytical technology, be more efficient in testing, reduce over-processing, enhance consistency, and minimize rejects. ... Click here

Podcasts
Manufacturing Equipment & Supplies
Filtration and single-use systems solutions and expertise.


Outsourcing & Consulting Services
Comprehensive GMP Bio/Pharma Product Testing.


Laboratory Equipment & Supplies
Caron’s New Extra-Large Capacity Environmental Chambers.


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