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Clinical Evaluation Reports (CER's) Required for All Classes of Medical Devices in Europe

Understand what is the CER and how to prepare for and defend it and properly constructing a "bullet-proof Technical File and manage your documentation.

By : Compliance Online
Product Type : On Demand Webinar
Strategic Software Validation Planning for Executives and Managers - Webinar

This training webinar will discuss how to approach Strategic software Validation planning so as to satisfy FDA by complying to new enforcement initiative by FDA.

By : Compliance Online
Product Type : On Demand Webinar
How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial

Understanding of IRB application components and how to find out and fix problem areas before it threaten your trial to fail.

By : Compliance Online
Product Type : On Demand Webinar
GCP violations and Site Mistakes commonly found During a FDA Investigator Site Inspection/Audit and how to avoid them

This GCP training will guide you through key component identification of a good GCP audit program, Investigator awareness, Protocol adherence, The Informed Consent process, Evaluation of subject selection, Inclusion/exclusion criteria, data sampling and audit findings assessments.

By : Compliance Online
Product Type : On Demand Webinar
Disinfectant Validation and Cleanroom Cleaning for all FDA and EMEA regulated companies

This training will teach how to choose the best disinfectants, know the different performance parameters of disinfectants, methods to qualify disinfectants, writing and executing cleaning procedures.

By : Compliance Online
Product Type : On Demand Webinar

> Previous Conferences, Webinars and Training All Past Conferences >

Pharma Summit 2016 – Risk Control & Compliance

The ComplianceOnline Pharma Summit 2016 - Risk control & Compliance aims to bring together FDA, Experts, Leaders and Veterans to discuss the most important challenges of Biotech, Pharma industry.

By : Compliance online

16 Jun, 2016 - 17 Jun, 2016
Pennsylvania / Philadelphia
Design of Experiments for Process and Product optimization

Attendees will learn to practice applying DOE techniques with various data sets. It will provide key tools and knowledge to be able to apply the methods effectively in their process and product development efforts.

By : Compliance online

16 Jun, 2016 - 17 Jun, 2016
Pennsylvania / Philadelphia
Overview of clinical drug development from final preclinical selection

Attend this seminar to design the most appropriate strategy for a clinical program, including all clinical developmental phases from IND to NDA/PLA.

By : Compliance online

2 May, 2016 - 3 May, 2016
Pennsylvania / Philadelphia