07.15.14 -- Lilly and Yabao To Partner For Diabetes Therapy; Hospira Acquires Orchid

Pharmaceutical Online Newsletter
Outsourced Pharma West Conference And Exhibition
November 10 and 11, 2014 | Hyatt Regency, San Francisco, CA

Who should attend? Pharma and biopharm executives who form and manage outsourcing partnerships.
What's on the agenda? Educational sessions focused on best practices and industry leaders’ experiences and lessons learned to help you avoid costly mistakes.

Register today! Space is limited. Brought to you by Life Science Leader magazine, BayBio, and Outsourced Pharma.
» From The Editor
How To Prepare A Facility For The Biopharmaceutical Revolution
By Trisha Gladd, Editor, Pharmaceutical Online and Bioresearch Online
Drug discovery is an inherently inefficient process. It takes thousands of failed compounds before one can get approved as safe and efficacious, and this effort does not come at a low cost. Because of this, the industry is constantly looking for ways to bring safe, compliant, and profitable drugs to market faster and cheaper. Patheon facility in Brisbane, Australia, exemplifies the facility needed to survive the future of pharma. But how did they do it?
Featured Focus: Logistics
How Active Packaging Systems Can Provide More Than Temperature Control
By Trisha Gladd, Editor, Pharmaceutical Online and Bioresearch Online
With the cost of cold chain logistics expected to rise from 6.7 billion in 2012 to 10.7 billion in 2017, it is even more important for pharmaceutical manufacturers producing temperature-sensitive drugs to select the most effective packaging solution to ship their product.
WHITE PAPER: Securing The Global Pharmaceutical Supply Chain Against The Threat Of Counterfeit Drugs
WHITE PAPER: Utilization Of Customs Warehouses In The Clinical Trial Supply Chain
DATASHEET: Passive Mobile Transportation Couriers
By CSafe Global
BROCHURE: An Affordable Way To Ship Temperature-Sensitive Cargo
» Manufacturing
WHITE PAPER: Designing An Effective Pharmaceutical Containment Blending System
By Denise McIntosh, Custom Powder Systems
The same pharmaceutical intermediate bulk container (IBC) that is used for shipping and storage can also be used for blending.
WHITE PAPER: Considerations When Selecting Capsule-Filling Equipment
By John Van Tol, Harro Höfliger
When it comes to the topic of capsule filling, the first and most immediate issue to consider is the equipment used for this purpose.  Obviously, selection of the most suitable encapsulator is an extremely important consideration. There are several questions you need to ask while working through the selection process.
SERVICE: Contract Metal Detection Services
WHITE PAPER: QC Testing: Quality Control Methods That Make A Difference
By Robert McGregor, Brookfield Engineering Laboratories, Inc.
How do you bring consistency to QC testing? Pharmaceutical products that meet manufacturability criteria and provide high-level consumer satisfaction undergo a battery of tests before being distributed to the consumer. Using affordable instrumentation to perform QC tests, which certify that tablets, capsules, elixirs, ointments, etc. have the right physical properties, is essential for today's successful businesses.
WHITE PAPER: Improving Prediction Robustness From Hard And Soft Modeling
PRODUCT: Control GMP Content And Prevent Revenue Loss In Life Sciences Manufacturing
» Inspection
BROCHURE: Contract Vision Inspection Services (Tablets, Capsules)
BROCHURE: BlisterScan Leak And Seal Detection
PODCAST: Risks Of Pinholes And Leaks In Pharmaceutical Containers
» Packaging
WHITE PAPER: Container Closure Integrity Testing Method Development And Validation For Prefilled Syringes
By Lei Li, Eli Lilly and Company
Utilization of prefilled syringes as a preferred container closure system for biologics has been increasing. As a primary container closure system, prefilled syringes must provide an integral barrier that protects drug product stability and sterility throughout its entire shelf life. Drug manufacturers are required to check and demonstrate the system is capable of maintaining its microbial barrier integrity. In 2008, the FDA further promoted container and closure system integrity (CCI) testing as a component of the stability protocol for sterile products.
CASE STUDY: Meeting Technical Challenges In Desiccant Dispensing
BROCHURE: Checkweigher EWK 3000
» Critical Environments
BROCHURE: Industrial Washers And Sterilizers
BROCHURE: Industrial Washers: Ampoules, Vials, Cartridges, And Syringes
PRODUCT: Softwall Modular Cleanrooms
ChemOutsourcing is the largest U.S.-based API show, attracting annually 700 to 800 chemists from the pharmaceutical, biotech, and chemical industries. The show focuses on API development spanning early drug discovery through chemical development and commercial supply. Attendees are executive scientists from pharmaceutical companies responsible for sourcing starting materials, intermediates, and active ingredients, and experienced in working with contract research and contract manufacturing organizations. Learn more.

Process Validation Guide: Regulatory Expectations And Best Practices
Date: Wednesday, July 16, 2014 • Time: 1:00 pm to 2:30 pm EST

The Seven Characteristics Of A World-Class Supply Chain
Date: Tuesday, July 22, 2014 • Time: 1:00 pm to 2:30 pm EST

Building An Effective GMP Training System: A Risk-Based Approach
Date: Wednesday, July 30, 2014 • Time: 1:00 pm to 2:30 pm EST
» Most Recent News
Envirotainer Receives Full FAA Approval For The RKN e1 Container
France Says Avastin Is Viable, Less Expensive Alternative Treatment for AMD
Purdue Pharma's HYD Pain Drug Receives FDA Priority Review
Lilly And Yabao Ink Agreement To Co-Develop Diabetes Therapy
Hospira Seals Deal To Acquire Orchid
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