Global Compliance Panal
Outsourcing

GMP Perspectives on Working with Contracting Laboratories

1 Reviews
Views

Global CompliancePanel Webinar Areas Covered in the Session: * GLP requirements that are assigned to a test facility and cannot be transferred back to a client. * Responsibilities of the sponsor or client. * The quality agreement and what it should contain to protect the interests of both client and contractor. * Auditing the contractor for compliance with the GLP ot GMP. * What is ISO 17425 and what is its effect on contract laboratories and their clients?

Current Presentation

Please Rate This Presentation

Related Presentations

Featured Presentations

API Importation Panel
Org
Video
00:27:02

Pharma ChemOutsourcing

Discussion on the reform in FDA inspection of offshore pharmaceutical/API manufacturing.
Agilent Mass Q-TOF LC/MS
Org
Video
00:04:08

Sensitive, Accurate-Mass MS and MS/MS Analyses

Typical mass accuracy – sub-1-ppm MS and 2-ppm MS/MS rivals or exceeds that of much more expensive FTMS and orbital…

Particle Sciences, Inc.

Drug Development Services Nanosystems, Formulation, Analytic
www.particlesciences.com

Raman Spectroscopy

Specialists in high performance Raman Spectroscopy instrumentation
www.HORIBA.com/scientific

Formulation Development

Get to market faster, We excel Quality, Speed and Cost of delivery
www.Xcelience.com/Formulation

PharmaInfoSite Your B2B Marketing Solution

Place your dynamic content on PharmaInfoSite for quality branding and instant lead generation.
www.pharmainfosite.com/howitworks

Excipients by ISP

Featuring binders, disintergrants, coatings, and solubilizers.
www.isppharmaceuticals.com