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Computer System Validation: Step-by-Step Webinar

Learn computer system validation essentials and eight fundamental steps of implementation for cost saving. Understand the structure of validation plan, documentation of ongoing performance, structure of validation report.

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
3-hr Virtual Seminar - China: Compliance Processes for Life Science Products

This 3-hr virtual seminar on compliance processes for life science products in China will discuss the regulatory structure and requirements for compliance with Chinese SFDA regulations for Pharmaceuticals, Medical Devices, Biologics and Combination Products.

By : Compliance Online
Product Type : On Demand Webinar
Understanding Disinfectant Qualification Studies – How to Avoid Errors (WEBINAR)

This webinar on Disinfectant Qualification Studies will teach you disinfectant testing methodologies, provide examples of disinfectant efficacy tests and show how to troubleshoot problems related to disinfectant efficacy testing.

By : Compliance Online
Product Type : On Demand Webinar
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Understanding Disinfection and Cleanroom Cleaning in a FDA Regulated Environment

This 90-minute webinar on Disinfection and Cleanroom Cleaning will cover effective ways to rotate disinfectants, most current industry methods for applying disinfectants and effective methods for controlling residues.

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