The PharmTech team focused on its coverage of AAPS PharmSci 360 this week, conducting interviews with experts on a range of topics including formulation platforms, AI, amorphous solid dispersions, and animal studies.
|Articles|March 2, 2017
Federal Equipment Company
Advertisement
Thinking about equipment? Federal Equipment Company delivers huge price and lead time savings when you are sourcing top-brand pharmaceutical processing and packaging equipment for your operations. Shop from our vast, on-hand inventory of equipment that covers all of your needs from R&D, scale-up, and commercial production to facility support and utility equipment. Do you have equipment to sell? Contact us! When you think equipment, think Federal Equipment.
8200 Bessemer Avenue, Cleveland, OH 44127
marketing@fedequip.com
tel. 800.652.2466
INTERPHEX Booth #3110
Advertisement
Related to this article
Subathra Ramamoorthy, Veranova, on when to escalate to structural elucidation and pair orthogonal techniques when characterizing an impurity.
Manish Baviskar, Hubot CDMO, on ALCOA++ data integrity, model version change control, continuous monitoring, and human sign-off.
The agreement between CDER and OII with allow for coordinated marketing application assessments and inspections.
Manish Baviskar, Hubot CDMO, explains which AI skills validation engineers need first and why AI model updates must go through GMP change control.
Ron Filler, Drug Development Consultants, explains how USP's 1074 revision brings human-relevant safety science to formulators and excipient makers.
Nitin Kumar Swarnakar, PhD, global application lab manager at BASF, talks about spray drying for drying amorphous solid dispersions and Raman spectroscopy’s role as a quantitative analytical tool.
Aleksandra Zuraw, senior veterinary pathologist at Charles River, discusses how chain of custody, good laboratory practice, quality control, and validation are applied to digital pathology data used in drug development.
Advertisement
Advertisement