JOY MCELROY - Eventura

Writing Validation Master Plans – Best Practices for Writing a Compliant Document

Duration: 90 Minutes

3-Hour Virtual Seminar on Technical Writing for the Regulated Industries

Duration: 3 Hours

FDA VS HEALTH CANADA - SIMILARITIES AND DIFFERENCES BETWEEN THE TWO REGULATORY BODIES

Duration: 90 Minutes

Building a Robust Vendor Qualification Program for FDA Regulated Industries

PRE-REGISTRATION AVAILABLE If you want to have this training scheduled Live and Exclusively for your company, we will arrange it for you. Pre-Register now and pay only once the training is scheduled on your preferred days. Click on the button below to pre-register

US FDA DRUG REVIEW AND APPROVAL PROCESS

Duration: 60 Minutes

ESTABLISHING AND REGAINING CONTROL OF CLEANROOM

Duration: 90 Minutes

4-Hour Virtual Seminar on Good Laboratory Practices (GLPs) vs GMPs – Comparison and Contrasts

Duration: 4 Hour

3-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries

Duration: 3 Hour

Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing

Duration: 60 Minutes

3 Hour Virtual Seminar – Technical Writing For The Regulated Industries

Duration: 3 Hour

3-Hour Virtual Seminar on Effective Cleaning Validation Procedures - Best Practices

Duration: 3 Hour

Validation and Part 11 Compliance of Computer Systems – 3 Hours Virtual Seminar

Duration: 3 Hour

Effective and Practical use of FMEA For Risk-Based Approach to Computer Systems Validation

Duration: 90 Minutes

FDA Compliant QC and QA Practices – Creating a Perfect, Audit-Ready QMS

Duration: 90 Minutes

How to Ensure Your Foreign Vendors are FDA Compliant – Conducting Vendor Audits, Monitoring, and Using Checklists

Duration: 75 Minutes

FDA’s Adverse Event Reporting and Product Recalls

Duration: 75 Minutes

Auditing and Qualifying Suppliers and Vendors – An Effective Risk Based Approach

Duration: 90 Minutes

Quality Control Laboratory Compliance – cGMPs and GLPs – 6 Hours Virtual Seminar

Duration: 6 Hour

Technical Writing Training for the Regulated Industries

Duration: 90 Minutes

Process Validation Guidance Requirements, FDA, EU Annex 15, Qualification and Validation – 4 Hours Virtual Seminar

Duration: 4 Hour

FDA Regulations for Environmental Monitoring (EM) Program

Duration: 60 Minutes

FDA Regulations for Analytical Instrument Qualification and Validation – Comprehensive Best Practices

Duration: 90 Minutes

Laboratory Safety – All You Need to Know

Duration: 90 Minutes

Good Laboratory Practices (GLPs) vs GMPs – Comparisons and Contrasts

Duration: 75 Minutes

Advanced Auditing Strategies to Detect and Mitigate Data Integrity Risks

Duration: 90 Minutes

Analytical Instrument Qualification & Validation – Use of Excel and FDA Audit Preparation

2-Day Seminar Completed | Recording and Pre-Registration Available

Enhancing Quality Oversight in Pharmaceutical Contract Manufacturing Organizations

PRE-REGISTRATION AVAILABLE If you want to have this training scheduled Live and Exclusively for your company, we will arrange it for you. Pre-Register now and pay only once the training is scheduled on your preferred days. Click on the button below to pre-register

Process Validation Training Course (FDA and EU Annex 15: Qualifications And Validation)

January 25 - 26, 2024 | US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM