Pharmaceutical Technology EPR Monthly Issue:
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Pharm Tech
October 18, 2017
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PRODUCTION TRENDS

Considering Water Use in Pharma Manufacturing

Water shortages, testing, and effluent treatment are important issues for pharma manufacturers.
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Now Online

Using Simulation to Address Capacity Limitations: modeling tools help engineers optimize a facility.
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FROM THE GMP BEST PRACTICE ARCHIVE

Cleaning Validation in Continuous Manufacturing

A lifecycle approach can be used to develop GMP-compliant cleaning procedures for continuous manufacturing.
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Best Practices for Cleaning Validation Swab Recovery Studies

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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Cleaning of Dedicated Equipment: Why Validation is Needed

Although dedicated equipment does not pose a risk of cross-contamination by different API substances, a wide range of possible contaminants must be evaluated.
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Critical for the Pharmaceutical Industry
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PACKAGING

Improved Materials Enhance Parenteral Packaging

Manufacturers introduce innovations in glass and plastic packaging for injectables.
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More Packaging

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Editor's Picks

Machine Fills and Seals Pharmaceutical Powders in Glass Vials

Bosch Packaging Technology's AFG filling and closing machine for pharmaceutical powders in glass vials offers manufacturers a wide range of options.
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Laboratory System Delivers Ultrapure Water

The Arium Mini from Sartorius Stedim Biotech is a compact water system for laboratories needing low volumes of ultrapure water.
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Equipment Showcase

Leistritz manufactures twin screw extruders and systems for continuous mixing/devolatilization of API's with excipients. Lab scale and production scale equipment is available, and applications include melt extrusion and granulation. A variety of upstream and downstream equipment is available. Services include a process NJ development laboratory and ongoing training/workshops.
/ See this link for more info /

Savillex Corporation manufactures the Purillex(TM) line of fluoropolymer bottles. Available in both PFA and FEP, Purillex bottles are manufactured in a cleanroom environment using a proprietary stretch blow molding process. This proprietary process provides several key benefits, including superior long term sealing, lower trace metal background and greater reproducibility. The bottles are available in sizes up to 2 Liters.
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UPCOMING WEBCASTS

Accelerating Method Transfer: Effective Automation of Biological Assays
Live Webcast: Wednesday, November 8 at 11:00am EST
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Challenges in the Development of Complex Small-Molecule Drugs
Live Webcast: Tuesday, November 7 at 11:00am EST
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Analytical Challenges in Extractables Studies of Plastic Single-Use Bioprocess Bags
Live Webcast: Tuesday, October 31 at 11:00am EDT
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Excipient Selection to Enable the Performance of Skin Delivery Dosage Forms
Live Webcast: Wednesday, October 18 at 11:00am EDT
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ON DEMAND WEBCASTS

From Candidate to Clinic: Strategies to Select, Assess, Formulate, and Deliver the Right Drug Candidate in the Early Phase
On Demand
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Enteric Capsule Technologies to Help Fast-Track Pharmaceutical Drug Development
On Demand
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Spectroscopy Advances for Improved Reproducibility and Easier Compliance
On Demand
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Packaging Material and Packaging System Quality for Pharmaceuticals and Biologics
On Demand
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EVENTS

CPhI Worldwide

Oct. 24–26, 2017 | Frankfurt, Germany


2017 ISPE Annual Meeting & Expo

Oct. 29 – Nov. 1, 2017 | San Diego, CA


more events

eBOOK

Biologics and Sterile Drug Manufacturing 2017 eBook

New technologies, including single-use systems, are leading the push for faster production and higher titers. At the same time, ensuring quality in raw materials and water systems, and controlling contamination are paramount. In this Biologics and Sterile Manufacturing eBook, the editors explore key technology, process, and operational topics.


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