Knowledge Center

Article / Jun 01, 2017

Speeding Development and Reducing Costs with Analytical Quality by Design

Authors:
  • Antonio Ramos
  • Rui Loureiro
Source:
Pharma's Almanac, Q2 2017, June, 2017

Applying Quality by Design (QbD) principles to analytical method development leads to many benefits, such as a more efficient method development process, more robust and reliable analytical methods, and compliance with increasing regulatory requirements, including those pertaining to method lifecycle management.

Related links

Also in the Knowledge Center

Related Content

Continuous Tableting for Drug Product

ËÄÉ«AV´s pragmatic approach to bridging science with manufacturing is now being leveraged for continuous tableting and it is the key to ultimately providing high quality medicines and the success of your drug product.

Page
Read more

Particle Engineering for Inhalation and Nasal

ËÄÉ«AV is a global expert and recognized leader in particle engineering, an essential technology when developing inhalation drug products.

Page
Read more

Inspections History

ËÄÉ«AV sites are periodically inspected by the local and external authorities. All sites are FDA approved and with exception of New Jersey site all have EU GMP certificates.

Page
Read more