Fremont, CA: “GMP for Quality Control and Contract Laboratories” is the topic of a two-day seminar that NetZealous LLC, a leading provider of regulatory compliance trainings for a wide range of regulated industries, will be organizing through its premier brand, GlobalCompliancePanel in Mumbai. Dr. Ludwig Huber, Chief Advisor - Global FDA compliance at Agilent Technologies, will be the Director at this seminar, which is being held on January 23 and 24, 2017.It is absolutely essential for contract laboratories to maintain the required standards of Quality Control because of the risk their process involves: After testing and approval, drug products and Active Pharmaceutical Ingredients (APIs) are released to the market without further check.
More details about the seminar can be had from http://www.globalcompliancepanel.in/control/GMP-for-quality-control
This fact is the primary reason for which regulatory agencies such as the FDA, EMA and many others place the highest emphasis and priority on inspections of QC laboratories. This is also one of the main reasons for which a huge number of QC related 483's and Warning Letters get issued to companies that have problems with their implementation, despite the existence of cGMP regulations for a long time.
At this highly interactive two-day seminar, the Director, Dr. Ludwig Huber will offer to participants the regulatory background and guidelines needed for all critical areas of GMP compliance. He will update them with the latest requirements of this compliance document, which will help them understand and implement these.
As a result of the learning gained at this two-day course, participants will be able to:
o Learn about the regulatory background and GMP requirements for quality control and contract laboratories
o Understand and be able to explain their company's quality plan or laboratory compliance master plan
o Understand the difference between GMP and non-GMP laboratories
o Learn how to develop inspection ready documentation
o Be able to train others in their organization on GMP requirements
o Learn how to avoid and/or respond to the FDA inspectional observations and Warning Letters.
About the Director:
Dr. Ludwig Huber is Chief Advisor –Global FDA compliance at Labcompliance, a global on-line resource for validation and compliance issues for laboratories. He has been Chairman, presenter and panel discussion member at US-FDA Industry Training sessions and conferences, and served as team member of PDA's task force’s “21 CFR Part 11”, of US-FDA internal documents, and of the GAMP® special interest group on Laboratory Systems.
About NetZealous:
NetZealous, a Fremont, CA-registered organization, dba GlobalCompliancePanel offers a broad range of high quality regulatory and compliance-related professional trainings and services relating to medical devices, pharmaceutical, FDA, clinical trials, laboratory compliance, biologicals, drugs, food and biotechnology.
NetZealous offers professional trainings to Regulatory compliance, human resources, healthcare and IT professionals through its respective brands, namely GlobalCompliancePanel, TrainHR, MentorHealth and ITTtrainingCenter.
Contact information:
Call: 1-800-425-9409;
customersupport@globalcompliancepanel.com
Visit: http://www.netzealous.com/