Articles from Validation Times (April 1, 2008)

Title	Author	Type	Words
7-item 483 to device firm for acceptance /rejection of product.	Pickett, Joseph		409
ArthoCare Corporation clears FDA audit.	Pickett, Joseph		212
AvTech Laboratories receives clean audit.	Pickett, Joseph		372
CAPA procedures trip up Philips Lifeline.	Mashaw, Rebecca		378
Catalent Pharma cited for QC failures.	Mashaw, Rebecca		583
CBER in 2008 to focus on improving manufacturing and product quality, CBER director Goodman says.	Pickett, Joseph		481
FDA needs $70 million more per year to inspect foreign drug plants: Commissioner von Eschenbach.	Pickett, Joseph		1062
GSK failed to report trial data, letter states.	Mashaw, Rebecca		495
Hazard analysis simple, powerful method to identify risk, says Chatterjee.	Pickett, Joseph		843
Legislation could be most significant change in drug law since 1962: CDER's Throckmorton.	Pickett, Joseph		697
Novartis Vaccines fails to assure sterility, letter states.	Mashaw, Rebecca		833
Retro-Tech warned for QS, device design procedures.	Mashaw, Rebecca		558
Spinal USA hit with 14-item 483 for faulty design plan review.	Pickett, Joseph		585
Sterilmed passes FDA inspection.	Pickett, Joseph		262
U.S. Apothecary Labs warned for test procedures.	Mashaw, Rebecca		495