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March 02, 2017
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   Good Manufacturing Practices for Aseptic Filling of Biopharmaceuticals - Register now

Attend this webinar to learn about pharmaceutical packaging options and aseptic filling options, especially with biologics. We will review regulatory guidelines on aseptic filling and demonstrate how to mitigate the risks associated with having to sterilize individual components while reducing the number of variables associated with the Aseptic Fill process

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» Industry News
 
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» Featured Articles
An Interview With...David Lyon, Director of Research, Capsugel’s Bend, Ore. Facility
An Interview With...David Lyon, Director of Research, Capsugel’s Bend, Ore. Facility
Today, more than 10 products on the market include a spray-dried intermediate (SDI) as a component of their formulation – and there are hundreds more in development pipelines. With the fast-growing ... read more »
Diagnosing Protocol Amendment Experience to Drive Clinical Trial Performance
Diagnosing Protocol Amendment Experience to Drive Clinical Trial Performance
Changing or amending a protocol after it has been finalized is a common and widely executed practice. Amendments are implemented for many reasons including the introduction of new standards of care; ... read more »
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» Featured Announcements
14th Annual Biopharmaceutical Manufacturing Report and Survey.
14th Annual Biopharmaceutical Manufacturing Report and Survey.
Participate in the bio-industry's most in-depth, global benchmarking and analysis study: 14th Annual... read more »
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» Featured Video
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  Watch Video: IQPC Modality Solutions - Introduction with Gary Hutchinson
Watch Video: IQPC Modality Solutions - Introduction with Gary Hutchinson
http://www.modality-solutions.com - Modality Solutions provides insight into cold chain thermal packaging, transport validation, and logistics solutions in highly-regulated and tightly-controlled ... read more »
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  Watch Video: Interview with Michele Luche from AMRI at AAPS 2016
Watch Video: Interview with Michele Luche from AMRI at AAPS 2016
AMRI is a trusted partner for global contract research, testing and manufacturing services for the biopharmaceutical industry. Our specialized solutions include Drug Discovery, such as medicinal ... read more »

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» Featured Whitepaper
Sterility Method Development and Suitability Testing
Sterility Method Development and Suitability Testing
USP Chapter <797> ‘Pharmaceutical Compounding- Sterile Preparation’ requires high risk level CSPs to meet the requirement of ‘Sterility test’ <71> before they ... read more »
Navigating Common Clinical Supply Challenges for Asia- Pacific Regional Studies

The challenges associated with conducting studies in this region can and do vary by country and whether the study sponsor is a local company or not. ... read more »
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| Events
EVENT
  8th Proactive GCP Compliance
Philadelphia, PA –  04/05/2017
ExL’s Proactive GCP Compliance conference is the annual gathering of more than 100 senior-level clinical quality and clinical operations executives. ... event details »
EVENT
  Bioassays 2017: Scientific Approaches and Regulatory Strategies
Silver Spring, MD –  05/08/2017
The CASSS Bioassays Symposium presents a truly unique opportunity for attendees to interact with key industry thought leaders and discuss topics such ... event details »
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