trainings.lincolnhealthnetwork.com Open in urlscan Pro
2606:4700:20::ac43:4691  Public Scan

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Submission: On March 23 via manual from US — Scanned from DE

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Upcoming TrainingsContact
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QUALITY ASSURANCE MASTERS TRAINING


DISCOVER PROCESS IMPROVEMENT AND QUALITY MANAGEMENT WITHIN LIFE SCIENCES AND
PHARMACEUTICALS


UPCOMING DATES

April 19–20, 2023
Register
June 21–22, 2023
Register


SIGN UP FOR TRAINING ANNOUNCEMENTS!

Email*




YOUR PARTICIPANT BENEFITS

 * Understand the elements of the and how each subsystem is interconnected to
   the rest in order to meet GMP requirements
 * Conduct internal audits to monitor quality and apply corrective actions when
   appropriate

 * Evaluate SOPs, design controls, and validation protocols from a quality
   perspective and make revisions or improvements as needed
 * Organize and manage evaluation data to improve product quality and address
   customer complaints


HERE'S WHAT PAST ATTENDEES HAVE TO SAY:

This course was very informative. The instructor was extremely knowledgeable and
was obviously interested and passionate about helping the group learn. I was
very happy with the course and would recommend to my colleagues.”

— Boehringer Ingelheim 

The QA Masters Training Course provided by the Lincoln Health Network is an
excellent source of material both for newcomers and experienced QA professionals
- very informative and entertaining!”

— Progenics Cord Blood Cryobank

Super informative, Adrienne Leyland was a great instructor”

— TherapeuticsMD


ORGANIZATION BENEFITS

 * Operate a GMP compliant manufacturing operation that supports changes to
   facilities, equipment, and processes to support product improvement
 * Save money and ensure product quality by encouraging “quality by design”

 * Improve product safety and integrity through increased quality monitoring at
   all stages of the manufacturing process
 * Prepare for the FDA’s systems based inspection


AFTER THIS TRAINING COURSE, YOU WILL BE ABLE TO:

 * Track and organize data efficiently to improve the evaluation process
 * Apply effective documentation techniques through the product life-cycle to
   avoid confusion and manage changes
 * Integrate risk assessment activities into the product design process to meet
   expectations of “quality by design”
 * Identify crucial training issues to address job-specific compliance
   responsibilities

 * Demonstrate a proactive approach to quality and improve operational
   efficiency
 * Anticipate and meet FDA expectations for a compliant quality system
 * Incorporate risk-management strategy to quality systems application
 * Build a quality-focused culture and facilitate management support for quality
   systems processes

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