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  • Webinar All-Access Pass (Recording) Subscriptions
  • reduce-costs-for-compliance-with-data-integrity
  • Raw Material Requirements

Webinars

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Preapproval Inspection and Submission to the FDA

  • John E Lincoln
  • Jan 14, 2025

CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contrac ....

  • Roger Cowan
  • Jan 15, 2025

An Introduction to Pharmaceutical Packaging and Labeling

  • Michael Esposito
  • Jan 21, 2025

Excel Spreadsheets; Ensuring Data Integrity and 21 CFR Part 11 Compliance

  • David Nettleton
  • Jan 21, 2025

Implementing Human Factors in Manufacturing

  • Ginette M Collazo
  • Jan 28, 2025

How to Prepare a Standard Operating Procedure (SOP)?

  • Afsaneh Motamed Khorasani
  • Jan 28, 2025

Installation and Qualification of the Packaging Lines

  • John E Lincoln
  • Jan 31, 2025

Calibration and Validation of Equipment

  • John E Lincoln
  • Feb 4, 2025

Function, Preparation and Execution of Job Aids in the Pharmaceutical Industry

  • Michael Esposito
  • Feb 4, 2025

Trial Master File and Clinical Data Management Regulated by FDA

  • Carolyn Troiano
  • Feb 5, 2025

Data Integrity and Privacy: Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR

  • David Nettleton
  • Feb 5, 2025

EU Medical Device Regulation 2017/745

  • Juan M Campos
  • Feb 6, 2025

Designing an Effective Cleaning Validation for Reusable Medical Devices in Today's Regulat ....

  • Gerry O Dell
  • Feb 10, 2025

Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries

  • Joy McElroy
  • Feb 10, 2025

FDA Bioresearch Monitoring Inspection Program 2024

  • David L Chesney
  • Feb 12, 2025

Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements

  • Roger Cowan
  • Feb 12, 2025

US FDA, Canada Health Canada, Brazil ANVISA, Australia TGA, Japan MHLW - MDSAP & EU ISO 13 ....

  • Juan M Campos
  • Feb 20, 2025

Seminars

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In Depth EU Medical Device Regulation (MDR) 2017/745 Training

  • Juan M Campos
  • Virtual Seminar | February 24-25, 2025

SOP Writing, Training and Compliance in the Pharmaceutical Industry

  • Michael Esposito
  • In-Person Seminar | Wednesday, February 26, 2025 & Thursday, February 27, 2025

Audits - Self/Internal, Vendor and Regulatory Inspections

  • John E Lincoln
  • Virtual Seminar | Monday, March 03, 2025

21 CFR Part 11 Compliance for SaaS/Cloud Applications

  • David Nettleton
  • Virtual Seminar | March 05-06, 2025

Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR

  • David Nettleton
  • Virtual Seminar | March 05-06, 2025
  • 21 CFR Part 11 Compliance for SaaS/Cloud Applications
  • Statistical Elements of Implementing
  • Webinar All-Access Pass (Recording) Subscriptions

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