Top Stories
A reformulated version of Rose Bengal, PV-10, may be used to treat melanoma when injected directly into tumors.
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The lawsuit alleges EnzymeWorks and its founder engaged in willful patent infringement, misappropriation of trade secrets, and breach of confidence, in addition to other claims.
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Industry News
CPhI Russia 2016 planned for companies seeking pharma business opportunities in region.
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The Eppendorf and Science Prize for Neurobiology is a research prize of $25,000, given to young scientists for their contributions in neurobiology.
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Supplier News
Cirrus Pharmaceuticals will launch services for manufacturing cGMP materials for early-phase clinical trials at its Raleigh-Durham, NC facility.
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Curida entered into a partnership with René Bommer, PhD, founder and owner of pharmAccel Consulting.
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Bio/Pharma News
Company representatives said a bulk of the increase was due to strong sales of its bioprocessing products.
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Under the agreement, Caribou has granted IDT worldwide rights to commercialize CRISPR-Cas9 reagents under Caribou's intellectual property.
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Regulatory News
The program is intended to provide support to ongoing efforts in rare disease product development.
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Policy makers debate strategies for promoting access to less costly medicines.
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Cost Effective Solutions to Develop and Manufacture Product
INTERPHEX is a premier pharma, bio and medical device development and manufacturing event dedicated to Innovation, Technologies and Knowledge throughout the full product development life cycle. Join us in New York, April 26-29, 2016. Register for your complimentary Technical Education and Exhibit Hall Pass Today at  www.INTERPHEX.com/Register. Discover what's NEW at #INTERPHEX. |
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Natoli Engineering Company, Inc., maintains a large selection of replacement parts for nearly every tablet press on the market ready for immediate delivery worldwide. By stocking replacement parts, up to 50% less cost than the original equipment manufacturers, Natoli is able to provide the highest quality parts at exceptional prices, faster than anyone else in the industry with next-day service!
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Webcasts
On Demand
Poorly-soluble APIs present formulation and development challenges. Excipient selection and manufacturing process development are crucial. Continuous twin-screw granulation is gaining acceptance as a manufacturing technology to address issues presented by these APIs and offers high production capacity in a small footprint. Learn how to improve the solubility of poorly water-soluble active ingredient using twin-screw wet granulation and proper excipients.
Sponsored by BASF
On Demand
Ion exchange resins have long been in the formulator’s toolkit, but only recently have they been used as excipients. Learn the value and benefits ion exchange resins bring to drug formulation challenges such as taste masking, abuse deterrence, controlled release, and more.
Sponsored by Dow
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How will you respond when the FDA asks: “Are you effectively monitoring your subcontractors?”
LIVE WEBCAST: Wednesday, March 23, 2016 at 8 am PDT / 10 am CDT / 11 am EDT
Join this informative webinar to learn how to foster relationships with contract partners to develop a quality surveillance program that will meet FDA scrutiny.
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on pharmtech tv
Addressing Drug Quality: Aging Facilities
Contract Services Market Trends
Working with CMOs and CDMOs
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Events
March 14-16, 2016
April 26-28, 2016
June 6-8, 2016
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Engineering the Mechanical properties of Amorphous Spray-Dried dispersions
On Demand
Capsugel Dosage Form Solutions will present a webinar discussing the aspect of engineering spray-dried dispersion properties, with a particular emphasis on the impact of atomization and drying rate on powder mechanical properties.
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REFERENCE BOOKS |
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A compilation of articles in a three-handbook set covering general Analytical Testing and Stability in the manufacture, packaging, storing, and testing of formulated products.
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Best Practices for Effective Product Transfer
On Demand
Understanding all aspects of the product transfer process is critical to a successful transfer and delivery of a quality product. During this one-hour webinar, regulatory and pharma experts will discuss the critical elements and processes needed for an effective, compliant product transfer process and successful end results.
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eBOOKS
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This eBook features articles on sterility testing, disposable technologies, parenterals, facility planning, mAb formulation, and more.
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