Pharmaceutical Technology EPR Monthly Issue:
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Pharm Tech
September 21, 2016
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PRODUCTION TRENDS

Making Use of Process Data

Manufacturing data collected in the process historian can be analyzed to better understand the process and use past behavior to predict future results.
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Now Online

Optimizing HVAC Systems to Improve Energy Efficiency
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TROUBLESHOOTING

Maintaining Hygienic Diaphragm Valves

A process-specific preventative maintenance program improves productivity and reliability.
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More Troubleshooting

Interphex
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EXPERT INTERVIEW

David Mayers, president of Wellspring Pharma Services, sat down with Pharmaceutical Technology to discuss the manufacture of controlled substances.

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Webcast

New Trends in Hygienic Diaphragm Valves that Improve Reliability

Live Webcast: Thursday, Sept. 22, 2016 at 11:00 AM EDT

The biopharmaceutical industry is under constant pressure to increase productivity, extend preventative maintenance intervals, and reduce overall operating costs—all without affecting product quality or purity. One area where performance can be improved is in the reliability of the facility's hygienic diaphragm valves.
Sponsored by: ITT Engineered Valves

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PACKAGING

Innovations in Cartons, Labels, and Inserts

Award-winning drug packaging innovations include interactive cartons and multifunctional labels.
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FDA's Proposed Generic-Drug Labeling Rule: Ensuring Efficiency and Compliance

If FDA's proposed generic-drug labeling rule is passed in 2017, generic drug companies would need documented processes for safety tracking and label updates.
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More Packaging

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Video: Outcomes of Continuous Improvement Driving Technological Advances with the Elastomer Closures
Recorded Live at INTERPHEX 2016, Presented by West Pharmaceutical Services
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Editor's Picks

Anticounterfeiting Label Prevents Container Reuse

Schreiner MediPharm’s Flexi-Cap Plus incorporates a label-integrated tear strip for enhanced security.
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Video: Product Demonstration
Meissner Presents at INTERPHEX 2016, Recorded Live
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Controller for Stability Chamber Complies with Electronic Records Requirements

Cincinnati Sub-Zero's stability chamber controller is validated to comply with FDA guidance for electronic records and digital signatures.
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Video: A Revolutionary Innovation on Aseptic and Contained Transfer
Recorded Live at INTERPHEX 2016, Presented by GETINGE GROUP
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Electronic Batch Record Software Improves Equipment Integration

InstantGMP PRO 3.0 software integrates production scales with an electronic batch record system.
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Video: Solid Dosage Operations Training Program
Presented by Federal Equipment / Techceuticals at INTERPHEX 2016, Recorded Live
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SPONSOR SHOWCASE

World's Fastest Capsule Filling Machine

Fette Compacting's new FEC40 Capsule Filler produces up to 400,000 capsules/hr – nearly twice that of any other capsule filler. This dramatically elevated output is accomplished in a remarkably small footprint, making machine reconfiguration due to floor space unnecessary. The high performance-to-footprint ratio is due to Fette Compacting's patented Duplex Concept, which utilizes a mirrored capsule filling process and double-sided discharge.
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Natoli's NP-RD20 R&D Press Perfect for Testing Before Scale-Up

Natoli Engineering’s NP-RD20 Tablet Press is the perfect mobile press for testing before scale-up. Designed to help move from R&D to production with fewer delays, features include programmable parameters for precompression and compression force, automatic tablet ejection, multi-layering capabilities and 42 kN compression force.
/ Learn more about the NP-RD20 today! /

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

Rapid and cost-efficient metal catalyst analysis

The control of metal catalyst residues and other non-intentionally added elemental impurities during the manufacturing processes of drug products is crucial. S4 TStar®, the new flexible TXRF spectrometer enables the rapid and cost-effective 24/7 monitoring of catalysts according to upcoming US/EU Pharmacopeia regulations.
The S4 TStar® is a plug & play system without need for gases or other media.
/ Learn more /


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Video: VeriPac UBV Blister Package Inspection Demonstration
PTI Inspection Systems Presents Live at INTERPHEX 2016
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EVENTS

CPhI Worldwide

Oct. 4–6, 2016 | Barcelona, Spain

more events

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Video: Quantitative Inspection Solutions to Successfully Navigate USP <1207>
Recorded Live at INTERPHEX 2016, Presented by PTI Inspection Systems
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eBOOK

Bioprocessing and Sterile Manufacturing eBook

Read feature articles on accelerated scale-up for vaccine production, standards for air cleanliness classification, aseptic filling advances, a flexible approach to cleanroom design, a science-driven approach for microbial control, removing genotoxic impurities, regulatory enforcement, drug shortages, and validation of single-use shipping systems.


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