Data Integrity Training Seminars | CAPA, Compliance, Regulatory Seminars

Compliance Seminars

Latest Compliance Strategies for Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices

By: David R. Dills ,Director of Regulatory Services at CROMSOURCE.

  • 27-February-2019 To 28-February-2019 Location:San Francisco CA

2 Days Seminar FDA Trends in Compliance and Enforcement for Regulated Computer Systems

By: Carolyn Troiano ,ERP Project Manager/FDA Compliance Consultant.

FDA requires that all computer systems used to produce, manage and report on “GxP” (GMP, GLC, GCP) related products be validated and maintained in accordance

  • 28-February-2019 To 01-March-2019 Location:Richmond , Virginia

Writing Effective SOPs: The First and the Most Important Step Toward Systemizing your Business

By: Angela Bazigos ,CEO Touchstone Technologies Silicon Valley.

  • 07-March-2019 To 08-March-2019 Location:Burlingame CA

21 CFR Part 11 (Electronic Records/Electronic Signatures) Compliance for Computer Systems Regulated by FDA

By: Carolyn Troiano ,ERP Project Manager/FDA Compliance Consultant.

The FDA governs the computer systems used to collect, analyze, transfer and report data that is in support of human clinical trials required for drug

  • 11-March-2019 To 12-March-2019 Location:Philadelphia

Aseptic Processing Overview and Validation

By: Kelly Thomas ,Vice President, Americas Quality Operations at Stallergenes Greer.

  • 18-March-2019 To 19-March-2019 Location:San Diego CA

2 Days workshop Effective Compliance Strategies for Complaint Handling, Medical Device Reporting and Recalls

By: David R. Dills ,Director of Regulatory Services at CROMSOURCE.

An effective complaint handling system is an extremely important part of any quality system. Manufacturers should understand that any complaint received on a product shall

  • 28-March-2019 To 29-March-2019 Location:Philadelphia

2 Day Seminar : Quality Management System: A modern approach to designing, implementation and maintenance of a QMS

By: Mr. Amirpour ,ISO-9001, ISO-13485, and IRCA-certified Pharmaceutical QMS Lead Auditor.

  • 04-April-2019 To 05-April-2019 Location:Boston
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