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March 2019 [+] (10 total)
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Establishing Appropriate Quality Metrics
March 4 - 4, 2019
1pm-2:30pm EDT, Online Training
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EU Medical Device Regulation: Your Questions Answered
March 12, 2019
Toronto ON CA
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Reacting to “Human Error” – Moving Beyond “Retraining” As A Response
March 13 - 13, 2019
1pm-2:30pm EDT, Online Training
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Cleaning Validation – Lessons Learned in the Trenches
March 14 - 14, 2019
1pm-2:30pm EST, Online Training
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Best Practices in CMC Dossier Preparation – Facing Tough Challenges
March 15 - 15, 2019
1pm-2:30pm EDT, Online Training
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Customers Over Data – How to Design and Implement IoT Solutions that Put People Before Process
March 19, 2019
Toronto ON CA
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Use of Electronic Records and Electronic Signatures in Clinical Investigations Under 21 CFR Part 11
March 19 - 19, 2019
1pm-2:00pm EST, Online Training
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Clinical Quality Management Systems (QMS): Establishing A Practical & Compliant Program
March 21 - 21, 2019
1pm-2:30pm EDT, Online Training
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Developing a Part 11 Compliance Plan in Clinical Research
March 26 - 26, 2019
1:00 PM - 2:30 PM EDT
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Competency-Based Training in a GMP Environment – Results Based on Roles and Responsibilities
March 27 - 27, 2019
1pm-2:30pm EDT, Online Training
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April 2019 [+] (20 total)
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Compliance with the New ICH GCP Revision 2 Addendum
April 1, 2019
Fremont CA US
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Audit Trail Generation and Review 2019
April 1, 2019
Fremont CA US
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Supply Chain Traceability is Going Digital [What You Can Do to Prepare]
April 4, 2019
Fremont CA US
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Test Method Validation to Verify the Performance of a Medical Device
April 4, 2019
Fremont CA US
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Implementing a Robust Change Control Program – Key Elements for Process and Documentation Compliance
April 4 - 4, 2019
1pm-2:30pm EDT, Online Training
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FDA's New Import Program for 2019
April 9, 2019
Fremont CA US
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Authoring and Implementing Standard Operating Procedures (SOPs): Best Practices for Success
April 9 - 9, 2019
1pm-2:30pm EST, Online Training
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Diabetes & Endocrinology: What New and what Next
April 10 - 11, 2019
Rome IT
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Strategies To Prevent Manufacture And Distribution Of Substandard Medications
April 10, 2019
Fremont CA US
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Data Integrity: Compliance with 21 CFR Part 11
April 11, 2019
Fremont CA US
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Responding to Clinical Observations: Developing Robust Audit & Inspection CAPAs
April 11 - 11, 2019
Online Training; 1:00 - 2:30 PM EDT US
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How to Implement MDSAP-Requirements into your ISO 13485
April 15, 2019
Fremont CA US
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Aseptic Process Validation: Top-Tips for Compliance and Success
April 17 - 17, 2019
1pm-2:30pm EDT, Online Training
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Controlled Document System for a Life Sciences Manufacturing Plant
April 18, 2019
Fremont CA US
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Turn a Culture of Quality Into a Competitive Advantage
April 23, 2019
Fremont CA US
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Instructional Design for GMP Training – Improve Effectiveness and Measurability
April 23 - 23, 2019
1pm-2:30pm EDT, Online Training
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The MHRA Data Integrity Guidance Clarified: What it Means for Industry & Patients
April 24 - 24, 2019
1:00 PM - 2:30 PM EDT
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Essentials of Disinfectant Efficacy Testing – Ensuring Microbial Control
April 25 - 25, 2019
1pm-2:30pm EDT, Online Training
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Preparing eCTD Submissions: A Step-By-Step Guide
April 29 - 29, 2019
1pm-2:30pm EST, Online Training
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Medical Device Recalls – Keys To Implementing A Successful Approach
April 30 - 30, 2019
1pm-2:30pm EDT, Online Training
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