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Compliance Conferences

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Understanding the new FDA Guidance for Immunogenicity Testing

This webinar on the draft FDA Guidance for Immunogenicity Testing will cover recommended approach to design elements of assay development and validation parameters.

By : Compliance Online
Product Type : On Demand Webinar
The 21 Elements of a 510(k)

This 90-minute webinar will review the 21 basic elements that need to be addressed in the traditional 510(k) submission, as required by the FDA.

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
Trial Master File for Research Sites: Can You Pass FDA Inspection?

This course reviews the investigator TMF required and additional content for a clinical trial - the activities of set-up, maintenance, and quality control and assurance will be discussed, as well as common deficiencies and challenges.

By : Compliance Online
Product Type : On Demand Webinar
Unannounced FDA GMP inspections

This GMP inspection Webinar training will discuss how to prepare for an unannounced FDA GMP inspection and more over how to predict when they occur and how you should be ready to face it.

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