COURSE ID 2759

Understanding the Process Validation Life Cycle

AVAILABLE On-demand
90 Minutes

On-Demand

Offering Price
$ 295
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Team Training

When you need on-site attention, we’re not just here to help, we’re there to help—right by your side.

Individual courses are remarkably effective. But sometimes when you have a specific need, it helps to have expert guidance right in the room with you and your team.

In that case, we’re happy to design a custom training for your entire team, whether online—or on-site.

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Remember – at checkout you can choose to take this course On-demand. We offer a 10% group discount when you register 2 of more attendees (up to 10). Contact us for larger groups.

This 90-minute, accredited ON DEMAND training is intended to help you better understand and get familiar with best practices for Process Validation applicable for the highly regulated biological/pharmaceutical industry. This course is further intended to discuss the life cycle of the Process Validation system. You will learn when a process should be validated, the basic components of a Process Validation (IQ, OQ, and PQ) and how to write protocols and reports.

This online training will benefit professionals in the following industries:

– Pharmaceutical

– Biotechnology

– Medical Device

– Chemical Processing

– Food

– Cosmetics

– Biologics

Those working in such job functions as:

– Engineers

– Chemists

– Scientists

– Formulators

– Documentation Specialists

– Auditors

– Managers

– Technicians

In addition, all personnel working in departments such as Manufacturing, Operations, QA/QC, Engineering will find the course very beneficial.

 

 

course instructor

Danielle DeLucy, MS
Owner, ASA Training & Quality Consulting LLC

Danielle DeLucy, MS’s Courses
Danielle DeLucy, MS, is owner of ASA Training and Consulting, LLC which provides Pharmaceutical and Biologics based companies with training and quality systems assistance in order to meet Regulatory compliance. Prior to this role, Danielle has been in the industry for 23 years serving in numerous Quality Management Roles, such as the Director of Product Quality, the oversight of Sterility Assurance practices and provided QA oversight of numerous filling and packaging operations. Danielle began her QA career as a Quality Control Pharmaceutical Microbiologist at a contract laboratory where she performed various tests for their clients. In the years after, she has held positions in the Quality management arena while increasing her responsibility. She has helped to lead many Regulatory Health Inspections and was instrumental in the coaching process of her peers prior to any inspection. Currently, Danielle assists companies who are faced with warning letters, consent decrees and those wishing to improve compliance establish more robust quality systems so that the company can succeed.