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Podcasts

Applying Water Activity to Pharmaceutical Technology
March 25, 2015 at 11AM ET
Sponsored by Decagon Devices

Delivering Biologics with a Difference
(On Demand)
Sponsored by Baxter BioPharma Solutions

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Events

INTERPHEX 2015
April 21-23, 2015
New York, NY USA

RDD Europe 2015
May 5-8, 2015
Antibes, France

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March 19, 2015 PharmTech.com PRINT SUBSCRIBE DIGITAL SUBSCRIBE

News

FDA Sets Agenda for 2015 Guidance Development
Biosimilars, supply chain security, quality metrics, and elemental impurities headline guidance topics on FDA’s 2015 agenda.
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Cures Require Compromise
Initiatives to speed drug development must pass Congress and special interest groups.
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FDA Sets Policies to Enhance Drug Security and Safety
Manufacturers face new rules for tracing drugs through the supply chain and compounders face stricter standards.
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News

Kite Pharma Inks Deal to Spur Move into European T-Cell Market
Kite Pharma announced that it acquired T-Cell Factory B.V. in an effort to strengthen its T-cell portfolio.
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Valeant Adds $1 Billion to Salix Offer, Amid Bid Battle
Valeant announced that it would increase its original acquisition agreement with Salix to approximately $15.8 billion.
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News

NSF International Publishes National Standard for Excipient Good Manufacturing Practices
NSF's consensus-based standard incorporates multiple regulatory and industry requirements into a single rigorous standard for the manufacturing and distribution of pharmaceutical excipients.
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Learn best practices of successful tableting, and tips and tricks for avoiding common manufacturing problems at Basics of Tablet Manufacturing and Troubleshooting, March 24-26, 2015. Reserve your spot for this hands-on course taught by Natoli Engineering’s technical services and training experts that offers knowledge far beyond what can be learned in textbooks and webinars. Learn More

Penn Pharma Adds Contained Roller Compaction Equipment in South Wales
Penn Pharma's equipment addition meets growing need for continuous dry granulation and for handling of highly potent drugs.
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Advertisement:
Applying Water Activity to Pharmaceutical Technology
Live broadcast on: March 25, 2015 at 11AM ET
Learn basics of water activity and the role it plays in the chemical stability, microbial content, and physical properties of pharmaceutical products. Hear experts discuss compendial and regulatory requirements for water-activity determination, and practical applications of water activity in marketed pharmaceuticals.
Register free:
www.pharmtech.com/water

23andMe Adds Therapeutics Unit
The company will build an R&D team to find promising drug targets with genetic information submitted by customers in its database.
Click Here to Read More

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BIO Encourages Transparency with Support of Biologic Interchangeability Bill
BIO and the Colorado BioScience Association urge Colorado Governor Hickenlooper to sign a bill that will help patients gain access to interchangeable biologic products following FDA approvals.
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McNeil Hit with $25 million Fine for Adulterated Medications
McNeil-PPC pleads guilty in connection with adulterated infants' and children's over-the-counter liquid medications.
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Porvair Opens New Facility in Hampshire, UK
Porvair Filtration Group has opened a new facility in New Milton, Hampshire, United Kingdom, creating approximately 20 jobs. Member of parliament, Desmond Swayne, will officially open the 42,000-square-foot premises on March 20, 2015.
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Catalent Unveils New Organization to Speed Up Drug Development
Catalent Pharma Solutions, provider of drug delivery technologies and development solutions for pharmaceutical and healthcare products, announced that Sharon Johnson, senior vice-president, Global Quality & Regulatory Affairs, is to head the company’s newly formed Quality, Product Development & Regulatory Affairs organization.
Click Here to Read More


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Podcasts
Advertisement:
Pharmaceutical Technology presents its Process Analytical Technology resource guide combo
A compilation of informative, useful articles designed to help you meet the challenges of process analytical technology, be more efficient in testing, reduce over-processing, enhance consistency, and minimize rejects.
... Click here

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