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Pharmaceutical Water System: Design, Testing and Data Management 2021

  • Start Date: 01/11/2022
  • End Date: 01/11/2022

Validation Sampling Plans 2021

  • Start Date: 01/10/2022
  • End Date: 01/10/2022

Supplier Management with the new Medical Device Regulation EU MDR 745/2017 2021

  • Start Date: 01/10/2022
  • End Date: 01/10/2022

Transfer of Analytical Methods according to USP <1224> 2021

  • Start Date: 01/10/2022
  • End Date: 01/10/2022

Pharmaceutical Water System: Design, Testing and Data Management 2021

  • Start Date: 01/11/2022
  • End Date: 01/11/2022

FDA Compliance and Clinical Trial Computer System Validation 2021

  • Start Date: 02/17/2022
  • End Date: 02/18/2022

Clinical Data Management (CDM) 2021

  • Start Date: 02/16/2022
  • End Date: 02/17/2022

Building a Vendor Qualification Program for FDA Regulated Industries 2021

  • Start Date: 02/16/2022
  • End Date: 02/17/2022

How to Create Clinical Evaluation According to EU MDR 2017/745 Article 61 and Annex XIV? 2021

  • Start Date: 02/15/2022
  • End Date: 02/15/2022

Healthcare Fraud Webinar - False Claims, Stark, Anti-Kickback Statute 2021

  • Start Date: 12/13/2021
  • End Date: 12/13/2021

Using Controls and Segregation of Duties to Build a Bullet Proof AP Operation 2021

  • Start Date: 12/13/2021
  • End Date: 12/13/2021

Process Validation Requirements & Compliance Strategies 2021

  • Start Date: 12/10/2021
  • End Date: 12/10/2021

CMO Supplier Quality Agreements - How to Comply with New FDA 2021

  • Start Date: 12/09/2021
  • End Date: 12/09/2021

On the Alert: Crafting an Effective Incident Response Plan (IRP) 2021

  • Start Date: 12/09/2021
  • End Date: 12/09/2021

FDA Modernization and Restructuring of the SDLC for Computer System Validation 2021

  • Start Date: 12/09/2021
  • End Date: 12/09/2021

Lone Worker Safety Compliance 2021

  • Start Date: 12/09/2021
  • End Date: 12/09/2021

Federal Oversight of Laboratory-Developed Tests in Limbo 2021

  • Start Date: 12/08/2021
  • End Date: 12/08/2021

Federal Oversight of Laboratory-Developed Tests in Limbo 2021

  • Start Date: 12/08/2021
  • End Date: 12/08/2021

Introduction to Medical Device Quality System Regulations 2021

  • Start Date: 12/08/2021
  • End Date: 12/08/2021

Validation Master Plan - The Unwritten Requirements 2021

  • Start Date: 12/07/2021
  • End Date: 12/07/2021

How to Achieve a Compliant and Effective Cleanroom Design and Facility Validation 2021

  • Start Date: 12/07/2021
  • End Date: 12/07/2021

How To Build a Profitable Generic Pipeline Before Your Competition 2021

  • Start Date: 12/07/2021
  • End Date: 12/07/2021

FDA's Ambitious Regulation of Social Media 2021

  • Start Date: 12/07/2021
  • End Date: 12/07/2021

Non-conforming Materials and Failure Investigations for Medical Devices 2021

  • Start Date: 12/06/2021
  • End Date: 12/06/2021

Strategies To Prevent Manufacture And Distribution Of Substandard Medications 2021

  • Start Date: 12/06/2021
  • End Date: 12/06/2021

An Update on Discharge Planning Rules and Regulations for 2022 2021

  • Start Date: 12/06/2021
  • End Date: 12/06/2021

Quality Control Laboratory Compliance - cGMPs and GLPs 2021

  • Start Date: 02/09/2022
  • End Date: 02/10/2022

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance 2021

  • Start Date: 02/07/2022
  • End Date: 02/08/2022

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance 2021

  • Start Date: 01/27/2022
  • End Date: 01/28/2022

The Drug Development Process from Concept to Market 2021

  • Start Date: 01/24/2022
  • End Date: 01/24/2022

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Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR 2022

  • Start Date
  • Mon, 05/16/2022 - 09:00

Supplier and Contract Manufacturer Management for Medical Device Manufacturers 2022

  • Start Date
  • Mon, 05/09/2022 - 08:00

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance 2022

  • Start Date
  • Thu, 04/28/2022 - 07:00

4th Edition of Euro-Global Conference on Food Science and Technology 2022

  • Start Date
  • Mon, 09/12/2022 - 08:00

Project Management for FDA-Regulated Companies 2022

  • Start Date
  • Wed, 03/30/2022 - 10:00

ANDA Submission and GDUFA Guidance 2022

  • Start Date
  • Mon, 03/28/2022 - 10:00

21 CFR Part 11, FDA's Guidance for Electronic Records and Electronic Signatures 2022

  • Start Date
  • Thu, 03/24/2022 - 10:00

The Physician Advisor's Role in Case Management 2022

  • Start Date
  • Wed, 03/23/2022 - 10:00

Reviewing Drug Product Batch Records 2022

  • Start Date
  • Fri, 03/18/2022 - 10:00

Marketing to Medicare or Medicaid Beneficiaries - What You Can and Cannot Do 2022

  • Start Date
  • Wed, 03/16/2022 - 10:00

FDA's Ambitious Regulation of Social Media 2022

  • Start Date
  • Tue, 03/15/2022 - 10:00

Promoting and Advertising Dietary Supplements in Compliance with FDA and FTC Regulations 2022

  • Start Date
  • Tue, 03/08/2022 - 10:00

How to Prepare a Standard Operating Procedure (SOP)? 2022

  • Start Date
  • Tue, 03/08/2022 - 10:00

Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation 2022

  • Start Date
  • Thu, 04/21/2022 - 09:00

Process Validation Guidance Requirements 2022

  • Start Date
  • Thu, 03/31/2022 - 10:00

21 CFR Part 11 Compliance for SaaS/Cloud Applications 2022

  • Start Date
  • Wed, 03/16/2022 - 08:00

Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR 2022

  • Start Date
  • Wed, 03/16/2022 - 08:00

Healthcare and Pediatric Nutrition Conference 2022

  • Start Date
  • Fri, 08/26/2022 - 10:00

26th International Conference on Food Fraud & Safety 2022 Vancouver Canada

  • Start Date
  • Thu, 10/27/2022 - 10:00

International Conference on Alzheimer and Dementia 2022 Paris France

  • Start Date
  • Wed, 03/09/2022 - 09:00

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