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Understanding and Implementing FDA’S 21 CFR Part 11-webinar

Understand 21 CFR Part 11 requirements and get a guidance how implement it in a cost effective way. Briefing about part 11 inspections.

By : Compliance Online
Product Type : On Demand Webinar
How to withstand an FDA audit of your facilities: A primer for clinical sites, manufacturing facilities

This webinar training will discuss the types of audit and what are the activities to be done before, during and after FDA audit to pass it successfully and how to increase credibility for your company.

By : Compliance Online
Product Type : On Demand Webinar
Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs

This Medical device training will be discussing the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing products.

By : Compliance Online
Product Type : On Demand Webinar
Calibration and Qualification in Analytical Laboratories Webinar

This webinar will provide a detailed understanding about calibration and qualification of laboratory equipments, development of a qualification master plan, allocation of equipments to qualification categories A, B, C, and the approach for qualifying existing systems.

By : Compliance Online
Product Type : On Demand Webinar
Equipment Calibration, Maintenance, and Validation: What Auditors Look for in a Controlled Proce

This webinar will discuss the different aspects which auditors generally look in equipment calibration, maintenance and validation and highlight the best practices.

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