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Welcome to Biofind events. Here we provide a list of events which have been registered with us, as well as a calendar view of upcoming events. If you want to post an event with us click here.

Event Location
Assessing FDA’s Proposed Changes to the 510(k) Process in 2011 - Medical Device Webinar By ComplianceOnline More details
Device Master Record & Device History Record – requirements, contents and implementation - Webinar By ComplianceOnline More details
How to transfer QC procedures for commercial products in pharma industry - ICH and USP guidelines - Webinar By ComplianceOnline More details
Full Day Virtual Seminar - Understanding Biofilm and Controlling It in Pharmaceutical Water Systems More details
Eliminate the Confusion – Annex 13 GMP guide More details
Establishing Global Drug Substance and Drug Product Specifications - Pharmaceutical Webinar By ComplianceOnline More details
Reduce COTS Software Validation using the risk-based approach - FDA Validation Webinar By ComplianceOnline More details
Excel Spreadsheets; develop and validate for 21 CFR Part 11 compliance - FDA Validation Webinar By ComplianceOnline More details
The CLIA Laboratory Inspection: Failure is not an Option - Clinical Webinar By ComplianceOnline More details
Ethics, Standards and Identifying Risks in Clinical Research - Clinical Webinar By ComplianceOnline (January 27, Thursday 10:00 AM PST | 01:00 PM EST) More details