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Heading to INTERPHEX 2015?
Check out our Real-World Serialization session on April 21 at 11:15 am, and learn more about Advances in Tableting on April 21 at 2:15 pm at the PharmTech/BioPharm Stage. Don't forget to stop by to meet our editors at booth #1530!
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Vaccine Development and Production Challenges Manufacturers
Scientists and industry experts seek effective preventive therapies to combat global disease.
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| Removing Aggregates in Monoclonal Antibody Purification
Several chromatographic resins are available for downstream purification.
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Tools of the Trade for Preventing Drug Shortages
A new technical report guides bio/pharma companies in establishing a risk-based approach for prevention and management of drug shortages.
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A world-leading tablet compression solutions provider, Natoli Engineering Company uses the highest quality materials to create efficient, durable and highly performing tablet compression tooling. We manufacture all punch configurations including single-tip, multiple-tip, micro tab, exotic shapes, IMA Comprima, die table segments and more, from a variety of high-quality steel types and specialty coatings. Request a quote and view informative content on our website.
 Learn more
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| Study Finds Prescription Drug Spending Rose 13% in 2014
Spending on prescription medications reached $373.9 billion in 2014, representing the largest increase in 13 years.
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| FDA Offices Collaborate to Prevent Drug Shortages
Agency teams work together to encourage manufacturers to seek approval for previously unapproved drugs.
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Webinar: A Case Study of Effect of Binder Type on Dry Granulation and Tablet Compression Properties of a Model Formulation
Join Metrics Contract Services and Anshul Gupte, Associate Director of Pharmaceutical Development, on Thursday, April 30 at 2:00 p.m. EDT for a webinar discussing the impact of roller compaction processing parameters and resulting tableting properties of roller compacted granules. Featuring the Gerteis Mini-Pactor®. Register at metricsinc.com.
 Learn more
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Sartorius Stedim Biotech Launches New Single-Use Harvesting Technology for High Cell Density Cultures
The single-use clarification system eliminates centrifuges; harvesting can be performed in one step; and process robustness and predictability are ensured.
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| Hydra Biosciences Enters into Collaboration Agreement with Boehringer Ingelheim
Hydra Biosciences enters into an agreement with Boehringer Ingelheim to research and develop small-molecule TRP inhibitors for renal diseases and disorders.
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 15th Anniversary Celebration of CPhI China
Become an industry leader, Be part of Chinese pharma dream
The 15th CPhI China, together with the 10th P-MEC China, will be held at Shanghai New International Expo Center, on 24th June, 2015. After fifteen years' development, CPhI & P-MEC China has successfully become an important bridge between local companies and global pharmaceutical industry.
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EMA Releases Medication Error Guidelines
The European Medicines Agency releases guidelines for addressing and reporting risks associated with medication errors.
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| Indonesian Pharma Market Poised for Strong Growth
CPhI report notes that the Indonesian pharma market is on the brink of a regional manufacturing boom, with market capitalizations and company values rising.
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 Practical Guidance for Successful Maammalian Cell Banking and Cell Line Characterization
Live Webinar: Thursday, May 14, 2015 at 8 am PDT/ 11 am EDT/ 4 pm BST/ 5 pm CEST
Join us for this informative webinar, presented by the team at Eurofins Lancaster Laboratories, to
learn about the various aspects of cell banking and cell line characterization, including GMP production master and working cell banks, GMP non-production (e.g. bioassay) master and working cell banks, R&D cell banks or banking for end of production cells.
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Pfizer Announces PCSK9 Competitive Grants Program
The grants will be offered to investigators conducting research in the field of PCSK9 biology.
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Hospira Italy Facility Gets Warning Letter
FDA issues a Warning Letter to Hospira S.p.A. for GMP violations at the company's Liscate, Italy facility.
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Pharmaceutical Technology E-Book: Solid Dosage and Excipients
This e-book examines how advances in technology, equipment, excipients, analytical techniques, software, and manufacturing practices are facilitating the development, scale up, manufacturing, efficacy, and delivery of solid- and semi-solid dosage forms.
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Baxter Recalls IV Solutions
Baxter voluntarily recalls select lots of IV solutions due to possible particulate matter.
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DBV Technologies Receives FDA Breakthrough Therapy Designation for Peanut Allergy Treatment
As the prevalence of falsified medicines continues to increase, Switzerland is taking measures to secure its supply chain, such as the implementation of serialization.
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Practical Implementation of the New Elemental Impuritites Guidelines
Live Webinar: US: Tuesday, May 5, 2015 at 11:00 am EDT | EU: Tuesday, May 12, 2015 at 15:00 AM CEST
In advance of the implementation dates, companies need to assess the risks of potential elemental impurities in their process and materials streams. In this webcast, experts review the regulatory requirements of elemental impurities guidelines, outline practical recommendations to address implementation challenges, and discuss key considerations for analytical testing programs.
 Register for free at www.pharmtech.com/pt/impurities
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Catalent Pharma Solutions Joins PBOA
Cornell Stamoran, Catalent Pharma Solutions vice-president, is elected to the board of trustees of the Pharma & Biopharma Outsourcing Association.
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 The Importance of Data Integrity in a GXP Regulated Laboratory
Live Webcast: Wednesday May 27, 2015 at 11:00 EDT; 15:00 GMT; 16:00 BST; 17:00 CET
With increased inspection scrutiny on data integrity, it is critical that managers and scientists in GXP regulated laboratories understand the current regulatory position. Discover the criteria for data integrity and learn how to assess and improve laboratory data management processes to ensure compliance with current regulations.
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