Validate TOC as an Analytical Method for Cleaning Validation-OnlineWebinar

Wednesday, May 03, 2017 at 10:00AM - 1:00PM
Fremont, CA
Item Name Price Each Fee Each Items Left Qty to Buy
Live Session
Show Info
$250.00 $8.62 20

Super Combo Offer
Show Info
$500.00 $16.34 18

Special Offer
Show Info
$625.00 $20.20 20

Corporate Live Session
Show Info
$1,250.00 $39.52 10

Event Details

Description
Total Organic Carbon (TOC) is a useful analytical method for cleaning validation studies, including design, qualification and routine monitoring. While there may be some confusion with the industry and regulatory bodies about the use of this analytical technique, it is widely used because of certain benefits. The basis of TOC as an analytical technique will be covered, involving the various technologies currently utilized. Cautions in sampling and analyses will be discussed, including the appropriate use of blank and controls.

Objectives Of The Presentation
  • Understand the Chemical Basis of TOC Analysis
  • Learn how to set limits based on TOC
  • Learn how to validate TOC as an analytical method for cleaning validation purposes
  • Understand possible interferences from sampling and analysis
  • Optimization of TOC recovery for difficult to oxidize or solubilise compounds
  • Learn appropriate uses of TOC throughout the validation life cycle
  • Benefits of at-line and on-line sampling
Why Should you Attend
TOC (total organic carbon) analysis is one of the most common analytical methods used for cleaning validation in the pharmaceutical industry. This nonspecific method is typically used to detect the presence of organic residues on cleaned product contact surfaces. TOC analysis is rapidly becoming the analytical method of choice for cleaning validation for several reasons. Many pharmaceutical companies are developing cleaning validation methods based on a whole-product approach: a determination is made as to whether any residue is present without regard to its origin (including products, cleaning detergents, chemicals, solvents, by-products, degradants, and microbial contaminants). This method works well with TOC analysis, which can detect any API or cleaning agent residue that contains carbon in its molecular structure.

This webinar will demonstrate Total Organic Carbon (TOC) feasibility, method validation and transfer from the laboratory to the manufacturing floor, as well as reviewing a feasibility study of multiple, difficult to oxidise or low solubility organic compounds.

Areas Covered
  • Principles of Total Organic Carbon Analysis
  • Description of analytical approaches in different instruments
  • Reasons for using TOC and Situations where TOC is preferred
  • Setting limits based on TOC
  • Use of blanks and controls
  • Grouping strategies for Analytical method validation
  • Dealing with interferences and Optimization of TOC recovery for difficult to oxidize or solubilise compounds
  • Cautions to be taken in sampling and analysis
  • Use of TOC throughout the validation lifecycle
  • Regulatory issues
Who will Benefit
Attendance will be beneficial to personnel directly involved in the development of cleaning procedures, cleaning validation programs and plans. Additionally, those responsible for cleaning validation protocols and execution activities, including validation and laboratory personnel, as well as, beginning or seasoned operational personnel who will eventually participate in such efforts, will find this course particularly useful. This includes Analytical Method Development, Quality Control, and Quality Assurance personnel.

Individuals in management who interact with the above or communicate with regulatory agency inspectors to rationalize or defend cleaning validation programs will also benefit from attending this course.
  • QA and QC managers
  • QC Analysis Technicians
  • Disinfectant validation managers
  • Operations managers
  • Manufacturing operators
  • Clean room managers
  • Clean room operators
  • Personnel and contractors that clean and disinfect clean rooms
  • Regulatory compliance managers and environmental monitoring managers
  • EH&S managers
  • Validation Engineers and Specialist
For Registration
http://onlinecompliancepanel.com/webinar/TOC-ANALYSIS-CLEANING-VALIDATION-509928/MAY-2017-ES-EZEVENT

Note: Use Promo code WE3PL and get 10% off on registration (Valid till MAY 31st 2017)

Organization Details

Online Compliance Panel (OCP) creates and delivers comprehensive industry relevant training sessions. These sessions are simple, interactive and cost effective. We are a predominantly web based information exchange forum. Live interactions on compliance training make the process holistic and effective. OCP largely emphasizes in offering regulatory compliance training to compliance professionals on varied topics. These primarily include risk management, quality management, corporate compliance and other regulatory compliances. Some of our primary areas of focus include advancement and updates in regulatory compliance, best practices and market trends.

We strive to incorporate high standards in developing a culture facilitating exchange of ideas resulting in functional excellence. OCP believes in nurturing ideas and thought processes through innovative e-learning methodologies. Our products and services are designed to offer customized solutions to industry and market. We bridge the gap between experience and knowledge thus delivering original and creative content.

Our objectives of employing interactive mediums ensure effective communication and mutual exchange of ideas. OCP closely follows best practices and regulatory trends in the global compliance scenario. We also observe and communicate trends witnessed in FDA, ISO regulations, process and design validation. All updates and additions to important laws can be accessed by our customers in real time.

Our mission is to empower compliance professionals through effective online training sessions. Our world class training methodologies stem from comprehensive understanding of client requirements. The content conforming to FDA and ISO standards is developed by well qualified and experienced industry leaders. Our offerings will exceed expectations and add value to your investment.

The content in various categories such as medical devices, pharmaceuticals and biotechnology will raise the bar in terms of quality already on offer .We hope to contribute to the creation of responsible organizations creating benchmarks in quality, integrity and transparency.

Your Shopping Cart

Your shopping cart is empty.
Select your items and click "Add to Cart".

Online Event
38780 Tyson Lane, Apt 210
Fremont, CA 94536

Starts May 03, 2017 at 10:00AM - 1:00PM

Add to my calendar  

Contact Information

Organization: Online Compliance Panel LLC

Event Contact: OCP Panel

Phone: 15108575896