Training

GLP Training:

GLP basics:  A half-day course on the rationale for following Good Laboratory Practices for the purpose of improving laboratory output. It covers definitions, documentation requirements, and proper methods for data recording. This course is designed for in-lab scientists and technicians, and managers needing a refresher in GLPs, as well as new Study Directors.  The training can be tailored to academic institutions, faculty and/or graduate students.

GLP Roles and Responsibilities:  This course covers the GLPs for Study Directors, Sponsors, Principal Investigators and Participating Scientists. We evaluate real-life scenarios and reinforce, Who signs what document? And When? The required elements of protocols and final reports are described. Case studies of multi-site studies are reviewed. This course can be tailored to a company’s specific needs from one-day to two-day and significant input from in-house QA is encouraged. It is designed for Study Directors, Sponsors, Principal Investigators, Participating Scientists and Test Facility Management of companies that routinely conduct multi-site studies.

Introduction to GLP:  A two-day course that covers Good Laboratory Practices. In addition to definitions, required elements of documents, and roles and responsibilities, this course focuses on the FDA or EPA’s inspection and audit processes. Why must every sample be labeled properly? How much time does the Study Director really have after the close of the study to archive the data? Why can’t we assign two Study Directors to certain studies? Learn to think how an inspector thinks in evaluating the quality and integrity of laboratory data. This course is designed for Study Directors and Management and significant input from in-house QA is encouraged.

Good Research Practices:  A short-course for laboratories seeking to enhance the overall quality and reliability of their data.   This course is based on the principles of Good Laboratory Practices, but it serves scientists who are not required to submit results to a regulatory agency.   Research laboratories, academic teaching labs, forensic labs, and contract analytical labs can gain by taking this course.  Non-GLP companies can strengthen their reputation in their  industry, their patent processes, and product marketability.

How To Write SOPs:  A half-day course on writing effective Standard Operating Procedures.  This course includes the basic elements that should be present in each SOP, the writing basics of scientific detail and instructions, managing revisions, and formatting and grammar tips.


Microbiology Training:

Basics of Microbiology, "Bacteria for Beginners":  A half-day course for employees new to industrial microbiology. Microbiology terms, principles of QC and disinfection, water testing, preservative testing, and environmental monitoring are reviewed.  In addition, the basics of microorganisms, and how they relate to a clean production facility and a quality research environment are covered.  This is a good intro for technical personnel with little background in microbiology or for non-technical individuals who need training in specific areas of microbiology.


Antimicrobial Test Methods:  In-lab training on EPA FIFRA testing requirements for making antimicrobial product claims for disinfectants and sanitizers. AOAC Use-Dilution Test, AOAC Germicidal Spray Test, Non-Food Contact Sanitizer Test, Food Contact Sanitizer Test included. Other test method training available, including sterility, stability testing, environmental sampling, MIC, additional test methods specific to your facility's needs.