Jul 22, 2011
This DMFs (Drug Master Files) training will discuss the current review and enforcement climate within FDA and the manner in which drug master files (DMFs) are reviewed by FDA personnel.
Jul 22, 2011
This Medical Device training will be discussing the newly-updated requirements of the Medical Device Directives,
Jul 18, 2011
"Attendees will recieve a complimentary e-book of " How to write standard operating procedures and work Instructions", published by the Instructor in 2010.The e-book will be send out to attendees after the webinar.
Jul 18, 2011
Holders of the IND for new products i.e. the Sponsors. Also, Principal Investigators and sub investigators, Clinical Research Scientists Safety Nurses, Clinical Research Associates and Coordinators , Recruiting staff, QA / QC auditors and staff.
Jul 18, 2011
Who will benefit: Quality Control Laboratory Manager Warehousing Purchasing Managers Procurement Managers Laboratory Analyst Cost Accounting
Jul 14, 2011
Who will benefit : Quality Managers Quality Engineers Small business owners Internal and external auditors Management Reps FDA inspectors Consultants.
Jul 14, 2011
Areas Covered in the Session CAPA defined The capa life cycle CAPA requirements CAPA design CAPA documentation Who will benefit: (Titles) Quality managers Quality Engineers Process Engineers Manufacturing Engineers
Jul 14, 2011
Who will benefit : Quality Control Laboratory Manager, Warehousing, Purchasing Managers and Procurement Managers, Laboratory Analyst, Cost Accounting, IT, Documentation Management
Jul 14, 2011
Provide valuable assistance to those companies involved in the handling of powders, lyophilized products, solid pharmaceutical dosage forms, and dried foods. Quality Control Scientists Development Scientists Production Management Quality Assurance