2 day seminar : Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices

By: David R Dills ,Regulatory Affairs & Compliance Consultant.

Course "Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full

  • 30-June-2017 To 01-July-2017 Location:Boston,MA

2 Day Seminar Preparing for and Managing Successful FDA Inspections

By: David R Dills ,Regulatory Affairs & Compliance Consultant.

The course will go through what typically goes on during an FDA Inspection and will then cover how to prepare for, host and follow up

  • 13-July-2017 To 14-July-2017 Location:Boston,MA

2 days seminar : Strategic Compliance and Risk Management: GXP Compliance Strategies, FDA Inspections and State of Readiness and Assistance during Inspections/Post-inspection Correspondence & Meeting

By: David R Dills ,Regulatory Affairs & Compliance Consultant.

An Interative Workshop Presented BY WCS & David R. Dills

Course “Strategic Compliance and Risk Management: GXP Compliance Strategies, FDA Inspections and State of Readiness and

  • 13-July-2017 To 14-July-2017 Location:Boston,MA

Human Resource Audit 2 days Workshop

By: Ronald L. Adler ,President-CEO at Laurdan Associates, Inc..

Title: 2 days in person seminar : Human Resource Audit 2 days Workshop Start Date: 9/14/2017 End Date: 9/15/2017 HRCI Recertification Credit Hours Awarded: 14

Over the

  • 14-September-2017 To 15-September-2017 Location:Houston Texas

Ensuring Compliance with Marketing, Advertising and Promotional Requirements for Pharmaceuticals and Medical Devices 2017 : Two Day Seminar

By: David R Dills ,Regulatory Affairs & Compliance Consultant.

An Interative Workshop Presented BY David R. Dills -Global Regulatory Affairs & Compliance Consultant 

Course “Regulatory & Compliance Strategies: Marketing, Advertising and Promotion of Pharmaceuticals and

  • 14-September-2017 To 15-September-2017 Location:San Diego CA

2 Day Seminar Assuring Data Integrity in the Life Science industry

By: Chinmoy Roy ,BSEE, MSCS US FDA Expert Data integrity & CSV.

This interactive two-day workshop planned by WCS provides attendees the opportunity to interact with a Data Integrity Subject Matter Expert.  Filled with numerous case studies

  • 04-October-2017 To 05-October-2017 Location:Boston,MA

2 Day Seminar : How to write error free procedures and comply with GMP regulations

By: Ginette M. Collazo ,Ph.D, President, Ginette M. Collazo, Inc..

An Interative Workshop Presented BY WCS & Ginette M. Collazo, LLC.

Course"How to write error free procedures and comply with GMP regulations" has been pre-approved by

  • 19-October-2017 To 20-October-2017 Location:Tampa, FL

2 Day Seminar : eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada (COM)

By: Peggy J. Berry. ,MBA, RAC,President & CEO, Synergy Consulting (Ex-FDA Official).

An Interative Workshop Presented BY WCS & Peggy J. Berry, MBA, RAC, (Synergy Consulting)

Course"eCTD Submissions of IND and NDA/BLA to the US FDA, EU and

  • 02-November-2017 To 03-November-2017 Location:Philadelphia, PA

One Day Seminar: "Effective Responses to FDA-483 forms and Warning Letters on Quality Systems"

By: J. Lawrence Stevens ,Senior Regulatory and Quality Consultant at The FDA Group, LLC.

An Interative Workshop Presented BY WCS & J. Lawrence Stevens, RAC

Course “Effective Responses to FDA-483 forms and Warning Letters on Quality Systems“ has been pre-approved

  • 08-November-2017 Location:San Francisco, CA

1 day seminar :GMP’s in practice: quality systems, common sense compliance, and application

By: Ginette M. Collazo ,Ph.D, President, Ginette M. Collazo, Inc..

An Interative Workshop Presented BY WCS & Ginette M. Collazo, LLC.

Course"GMP’s in practice: quality systems, common sense compliance, and application" has been pre-approved by RAPS

  • 07-December-2017 Location:Washington D.C
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