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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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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
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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.

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Join 800+ peers for 4 days of learning and unparalleled networking in beautiful Southern California on March 30-April 2. Register now and SAVE $200 off the Standard Rate with Code: B15155KPG.
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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.

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.

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.

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.

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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.
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