There is a great need for sensitive, precise, and easily accessible analytical detection techniques for protein sequencing.

Biologics Quality Control: The Growing Need for Accessible Proteomics

The emergence of mRNA vaccines and cell and gene therapies has pushed innovation in analytical methods.

Emerging Therapies Drive Analytical Advancements

Effective analytics will eliminate failures, deviations, and non-conformances.

 Analyzing Exabytes

Topic

Articles

Company and People Notes: Pfizer Completes King Tender Offer; Cook Pharmica Names VP of R&D and CSO; and More

Week of Jan. 31, 2011: Company and People Notes: Pfizer Completes King Tender Offer; Cook Pharmica Names VP of R&D and CSO; and More.

Michelle Hoffman, editorial director of Pharmaceutical Technology.

Follow-ons were all the rage at this year's JP Morgan Healthcare Conference.

Follow-Ons: The New Black?

New products in tableting and granulation.

In the Spotlight February 2011

Q&A with Magnetrol International's Dan Klees

Q&A with Dan Klees, Magnetrol

Using risk assessment properly can provide industry with a unique tool for quality control.

The Promise and Threat of Quality Risk Management

Tim Freeman is Managing Director of powder characterization company Freeman Technology for whom he has worked since the late 1990s. He was instrumental in the original design and continuing development of the FT4 Powder RheometerÂ® and through his work with various professional bodies, and involvement in industry initiatives, is an established contributor to wider developments in powder processing.Tim has a degree in Mechatronics from the University of Sussex in the UK. He is a mentor on a number of project groups for the Engineering Research Center for Structured Organic Particulate Systems in the US and a frequent contributor to industry conferences in the area of powder characterisation and processing. A past Chair of the American Association of Pharmaceutical Scientists (AAPS) Process Analytical Technology Focus Group Tim is a member of the Editorial Advisory Board of Pharmaceutical Technology and features on the Industry Expert Panel in European Pharmaceutical Review magazine. Tim is also a committee member of the Particle Technology Special Interest Group at the Institute of Chemical Engineers, Vice-Chair of the D18.24 sub-committee on the Characterization and Handling of Powders and Bulk Solids at ASTM and a member of the United States Pharmacopeial (USP) General Chapters Physical Analysis Expert Committee (GC-PA EC).

How to adapt a real time release approach to powder processing during drug-product manufacturing.

Applying Real Time Release Testing to Powder Processing

Angie Drakulich was editorial director of Pharmaceutical Technology.

A roundtable moderated by Angie Drakulich.

Real Time Release Testing: Analytical Methods and Innovations

Novartis Acquires Genoptix; Lilly Exec Becomes Savient CEO; and More.

Week of Jan. 24, 2011: Company and People Notes: Novartis Acquires Genoptix; Lilly Exec Becomes Savient CEO; and More.

FDA published its long-awaited guidance titled Process Validation: General Principles and Practices this week.

FDA Publishes Revised Process-Validation Guidance

Merck Teams with Parexel; Roche CFO to Retire; and More

Analytics

Biologics Quality Control: The Growing Need for Accessible Proteomics

Emerging Therapies Drive Analytical Advancements

Analyzing Exabytes