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American Pharmaceutical News In Review
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November 29, 2017
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   The durability of plastic with the surface of glass.

SiO2 Medical Products has developed a new material and method of manufacturing for primary containers that solves the industry’s major problems associated with glass and plastic primary containers and addresses the requirements for emerging parenteral drugs. Traditional approaches to improve the performance of vials and syringes have reached their limits.

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» Industry News
 
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» Featured Articles
Second Level Thinking in Cleanroom Decision Making
Second Level Thinking in Cleanroom Decision Making
Articles like these generally have the same opening – a discussion of increasing expression rates ... read more »
Strategies to Predict the Developability of Biopharmaceuticals
Strategies to Predict the Developability of Biopharmaceuticals
Over the last decades drug development expertise for biologicals has constantly increased. read more »
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» Featured Video
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  On-Demand Webinar: Learn How Acoustic Liquid Handling Can Improve Your Bioassay Workflows
On-Demand Webinar: Learn How Acoustic Liquid Handling Can Improve Your Bioassay Workflows
In this webinar, we will compare acoustic droplet ejection (ADE) technology to standard tip-based liquid handlers. We will address how ADE can reduce ... read more »
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  Watch Webinar: The Importance of Binder Selection and its Impact on Tableting Results in Roller Compaction
The Importance of Binder Selection and its Impact on Tableting Results in Roller Compaction
Roller compaction is the manufacturing method of choice when the physical characteristics of the active do not allow for direct compression and wet ... read more »

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» Featured Products
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  ACQUITY UPLC I-Class System
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  TSQ Quantum XLS Ultra GC-MS/MS
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» Featured Whitepaper
Electronic Records on Instruments the Concept of 21 CFR Part 11 Without a PC
Electronic Records on Instruments the Concept of 21 CFR Part 11 Without a PC
Data integrity is a major topic in all laboratories and with good reason. The risks of noncompliance are high and losing important data can be costly. 21 CFR Part 11 is a regulation that defines the ... read more »
Whitepaper: Determination of Stress Conditions for Microorganisms for use in Validation of Milliflex Rapid Detection System
Determination of Stress Conditions for Microorganisms for use in Validation of Milliflex Rapid Detection System
In the pharmaceutical/biotechnology manufacturing industry, most of the microbial contaminants are believed to be stressed. read more »

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| Events
EVENT
  Achieving Efficient Facilities/Next Frontier for Single Use
San Diego, CA –  12/11/2017
Designed with Flexibility in Mind — Select Your Preferred Event or Attend Both for Maximum Value, Learning and Benchmarking The adoption of ... event details »
EVENT
  CSV & Data Integrity Compliance Congress
Washington, D.C. –  12/11/2017
Presented by KENX, this event showcases the protocols, methodology and actions necessary to avoid FDA regulatory action. Choose from over 32 tutorials... event details »

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