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Featured Articles
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Tighter pH Control In Chromatography And Purification Systems With Wireless Transmitters
By Emerson Process Management, Rosemount Analytical Liquid
Biopharmaceutical Chromatography Systems are designed
for separating and purifying proteins and bio-engineered
products. Flow systems are compact in design to maximize
throughput. No dead legs in process pipe can exist
since unswept areas are more challenging to completely
clean, and they delay product throughput by decreasing
flow rates. The systems must maintain a hygienic
design.
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Why, What, And How? Understanding The Freeze Drying Process
By Biopharma Technology Limited
With freeze drying, heat-sensitive drugs and biologicals can be dried at low temperatures. The avoidance of high temperatures helps to reduce the extent of decomposition or loss of activity in biological products, and can also circumvent the alteration of taste and sensory qualities in foods. Freeze-dried products have a very high surface area, which enables them to be reconstituted quickly and easily with the re-introduction of the solvent (usually water).
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Retrofitting Process Equipment Achieves Containment For A Range Of Manufacturing Operations
By ILC Dover
Retrofitting refers to the addition of new technology or features to older systems. This generic definition is somewhat basic, but it applies to enhancing process equipment and facilities. The key objective is to apply proven containment technologies to minimize the negative effects on production, while optimizing benefits to the organization.
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Characterization Of Medicinal Tablet Surface Area With The Gemini Series
By Micromeritics Instrument Corporation
Gas adsorption surface area values can predict
the reaction rate of compounds such as medicinal
products in tablet or powder form. The dissolution
rates of these products are directly
related to the magnitude of their surface areas.
Tablets and powders generally have low gas
adsorption surface area values.
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Monitor And Control On The Move: The Next Evolution In Factory Automation
By Motorola
When the mobile computer replaces the desktop PC as the information bridge
between the machine real-world network and your transactional business
systems, you move your operators closer to real time, closer to your machines,
and closer to the product that is being manufactured, increasing control over
the manufacturing process and overall profitability.
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Sponsor
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Norwich Pharmaceuticals
Norwich Pharmaceuticals provides a complete range of enhanced services and capabilities meeting full life-cycle pharmaceutical outsourcing needs, from clinical trial to commercial launch, and is one of the first companies to utilize the SupplyScape Corporation Nexus supply chain solution. Download the company brochure for additional information.
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Spotlight On Outsourcing
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Brochure: Encompass Analytical Services
Encompass provides state-of-the-art analytical services to some of the leading pharmaceutical companies in the world. Our extensive pharmaceutical experience provides for regulatory GMP/ICH/USP compliance along with scientific excellence. We bring you results with interpretation and direction to ensure your project's successful completion.
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Brochure: Confab Pharmaceutical Manufacturing And Technical Services
Confab's scientific services include an analytical laboratory extensively equiped for pharmaceutical testing of raw materials and finished products, in- house validation services, regulatory affairs, narcotics management, and all usual quality system management.
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Datasheet: Active Pharmaceutical Ingredient (API) Capabilities
The active pharmaceutical ingredient (API) is a key element of the drug
development process — all further development is dependent on its
supply. Given the integral role of API and Aptuit's commitment to
streamlining and supporting the drug development process, it is fitting
that Aptuit offers a wide range of API services on a global scale.
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Flyer: Complex Sterile Manufacturing
We are finding a qualified source for sterile
manufacturing — with state-of-the-art
capabilities and extensive expertise for
even the most complex pharmaceutical
and biopharmaceutical formulations —
covering everything from freeze-dried and
aseptic filling to a wide variety of vials and
prefilled syringes.
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Brochure: Contract Manufacturing Services For Sterile Pharmaceutical And Biotech Products
Catalent provides a full range of contract services from early clinical development through commercial manufacturing and packaging for sterile pharmaceutical and biotech products. Its expertise and experience cover a wide range of processes and sterile dosage forms.
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Brochure: ICON
Partnerships with CROs Booth #340
ICON is a global company with experience in the world's most important regions for clinical research. They specialize in the strategic development, management, and analysis of programs that support clinical development — from compound selection to Phase I to IV clinical studies.
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Featured Downloads
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Datasheet: Quick to Market™
A unique, Patheon-only program that offers accelerated transfer of commercially available products from an existing manufacturing plant to a plant within Patheon's network.
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Brochure: EZ-CFU™
EZ-CFU™ One Step, from MicroBioLogics Inc., is made to support growth promotion microorganism challenges that must meet USP/EP/JP guidelines. These lyophilized microorganism preparations are manufactured to perform within a predetermined range of 10 CFU to 100 CFU in a 0.1 mL volume.
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Case Study: Contractor Safety Management For Major Pharmaceutical Company
HazTek is currently in its fifth year as a member of the Top 10 Pharmaceutical Company's New Jersey Regional Contractor Safety Management team. Under this contract, HazTek serves as the primary representative for implementing, maintaining, and enhancing all aspects of its Contractor Safety Program throughout the region.
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Brochure: Quali-V® Pharmaceutical-Grade Hypromellose (HPMC) Capsule
Manufactured from plant-derived materials, the capsule meets the demands for nonanimal requirements and for the dietary sensitivities of certain markets. Quali-V® perfectly matches the pharmacopeial requirements for capsules in USP/NF, EP, and JP.
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Featured Multimedia
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| Video: Contract Pharmacal Coating |
| CPC uses high-speed, state-of-the-art processing equipment for on-time delivery and consistent batch results. CPC manufactures solid oral dosage forms, including tablets (uncoated, film-coated, enteric-coated, and sugar-coated); capsules, modified release tablets and capsules (extended release, delayed release, and long acting), pellets (immediate and time release seeds),
powders, and granules.
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Bulletin Board
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Free Webinar:
Optimizing The Clinical Trials Disclosure Process
April 16
11 AM (EDT)
Will you meet the new mandates and directives for clinical trials/adverse effects disclosure coming this Fall? This free webinar will reveal how you can predictably and consistently prepare quality submissions designed to meet these internationally disparate disclosure requirements.
Register here.
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Industry Events
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Featured Courses From The Center For Professional Innovation And Education
How To Monitor Clinical Trials For GCP Compliance
April 14 and 15 | Malvern, PA
Comprehensive Overview Of FDA Regulatory Compliance For Drugs And Biotech Products
April 15 and 16 | Malvern, PA
Validation Of Computer Systems
April 20 and 21 | Costa Mesa, CA
Reporting Failure Investigations and Process Deviations
April 20 to 22 | Malvern, PA
Pediatric Clinical Trial Design: Ethics, Management, And Regulatory Requirements
April 20 and 21 | Malvern, PA
Other Events:
LogiPharma Europe 2009
April 21 to 23 | Geneva, Switzerland
Powder And Bulk Engineering: 2009 Southeast Conference And Exhibition
April 28 to 30 | Atlanta, GA
ACHEMA 2009
May 11 to 15 | Frankfurt, Germany | | | |
