ComplianceOnline

Guidelines for Good Practice in the conduct of Clinical Trials in South Africa

  • Date: December 08, 2009
  • Source: www.doh.gov.za
Webinar All Access Pass Subscription Abstract:

Clinical trials on Human participants needs strict vigilance and is conducted under high standards of quality assurance. Quality assurance of clinical trials in South Africa is achieved at a number of levels, through monitoring, audits and inspections. Clinical trials are a joint responsibility of the sponsor and the investigators. A proper comunication channel has to be established between the sponsor and the invetigators at every stage of the trial. Regular audits are necessary to ensure proper processes are followed and all regulatory compliances are considered. Independent regulatory authority may conduct announced or unannounced inspections at any stage of the trial to review the competency of the clinical trial site.

Bookmark and Share

Trending Compliance Trainings

Trial Master File and Clinical Data Management Regulated by FDA
By - Carolyn Troiano
On Demand Access Anytime
Good Documentation Practice and Record Keeping Regulations (FDA & EMA)
By - Dr. Afsaneh Motamed Khorasani
On Demand Access Anytime
GAMP Data Integrity 21 CFR Part 11 Training Course
By - Kelly Thomas
On Demand Access Anytime
NEW Reclamation Process - Fed Gov't Payments
By - Donna K Olheiser
On Demand Access Anytime
Understanding and Preparing for FDA Pharmaceutical Inspections
By - Michael Ferrante
On Demand Access Anytime
How to conduct an effective BSA Audit
By - Justin Muscolino
On Demand Access Anytime
Installation and Qualification of the Packaging Lines
By - John E Lincoln
On Demand Access Anytime
Best Sellers
You Recently Viewed
    Loading