Celeste Rose, RQAP-GLPRoseTECH Consulting provides GLP Training, Quality Assurance, and Consulting services to the Life Science and Specialty Chemicals industries.    

2014  RoseTECH Public Webinars

Achieving Reconstructible Documentation Practices
Good, Bad, Ugly-Amendments, Deviation, Circumstances
GLP Standard Operating Procedures
Multi-Site Studies
GLP Equipment Requirements
ffective Writing of Protocols & Reports
GLP Roles & Responsibilities
Test/Control Articles and Dose Analysis
Interested in a private WEBINAR specialized for your organization?

Attendees overwhelmingly recommend Celeste’s training webinars & workshops
Below are just some of the testimonials from prior training sessions:

  • “Celeste is a very knowledgeable and experienced Subject Matter Expert.”
  • “Very knowledgeable instructor. She was able to give specific examples relating to her subjects. I enjoyed her presentations.”
  • “Well-informed about the material.  Well-organized slides mixed with interesting examples based on her experience.”
  • “Very informative… makes you really think and remember the rules.”
  • “Great fun… good discussions… a lot of content with a variety of fun.”

FAQ Article!
Frequently Asked Questions – Amendments, Deviations, Unforeseen Circumstance



  • GLP & Technical Training
  • Study Auditing & Inspections
  • Test Facility Inspections
  • CRO/Subcontractor Inspections
  • 3rd-Party Independent Audits
  • GLP Start-up/Transition to GLP
  • Quality System Implementation
  • SOPs/Technical Writing/Review
  • QA Management
  • Study Director/Principal Investigator
  • SOP, Protocol & Report Writing
  • Archiving & Document Control
  • Toxicology & Metabolism
  • Dose Analysis, Prep & Administration
  • Method Validation
  • BioAnalytical, TK/PK