NetZealous LLC announces seminar by Dr. Ludwig Huber though its brand, GlobalCompliancePanel, on the topic, “GMP for Quality Control and Contract Laboratories”

Fremont, CA, 2016-Aug-16 — /EPR Network/ — “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:

• Learn about the regulatory background and GMP requirements for quality control and contract laboratories
• Understand and be able to explain their company’s quality plan or laboratory compliance master plan
• Understand the difference between GMP and non-GMP laboratories
• Learn how to develop inspection ready documentation
• Be able to train others in their organization on GMP requirements
• Learn how to avoid and/or respond to the FDA inspectional observations and Warning Letters.

In addition, the Director will also be providing participants with templates and examples with which  they can develop inspection ready documentation. Another of the highlights of this session is that practical examples and interactive exercises will be sprinkled into and between the presentations, with half of the duration of the seminar being dedicated for practical sessions.

Taking the interactive element a step further, Dr. Huber will arrange participants into small groups for the purpose of discussing case studies and prepare the answers using prepared fill-in templates. Yet another bonus of this session is that after the course, Dr. Huber will make a large variety of tools such as SOPs, validation examples and checklists readily available on a dedicated website so that those who have attended this seminar can use them to easily implement what they have learned from the course.

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.

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According to Satisha Naraharimurthy, Founder and CEO of NetZealous, this seminar is very important for the important learning it imparts to professionals about Quality Control for contract laboratories. “With outsourcing gaining such importance over the past few years, it is very important for contract laboratories to get the entire Quality Control process right, failure at which can adversely impact a number of players. Our seminar will serve a very important purpose of helping participants understand the elements of Quality Control in contract laboratories”, he said.

Shahanshah Manzoor, Co-Founder and Chief Marketing Officer at NetZealous, said: “NetZealous has always strived to offer courses that are relevant and valuable. This is one of them. Participants who have taken this course will be able to implement a very, very critical aspect of contract laboratories: Quality Control. This will help them tide over the difficulties associated with this kind of working relationship”.

“Contract laboratories are highly preferred for the cost saving they bring about. But in the absence of Quality Control, their products can cause havoc to the lab, the general public and many other stakeholders. The aim of this seminar is to teach participants how to get their whole contract aspect right”, said Liju Mathew, Co-Founder and Chief Business Development Officer at NetZealous LLC.

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: 1800 425 9409 ;

Visit: http://www.netzealous.com/