Laboratory Inspections - Be Prepared, Be Validated and Avoid Observations

Course Description:

In every laboratory inspection there are always two teams – the auditors and the auditees. Whether you are performing the audit or receiving the audit, there are rules, techniques and tips that will make your job more effective and reduce audit observations. This interactive and exciting seminar will look at various laboratory audits (GLP, cGMP, GCP, EPA) from both perspectives. You learn what auditor s look for, see examples of best practices and also hear war stories of things gone wrong as you get to experience both sides of the process. We will use presentation, discussion, exercises, role playing and workshops so that you experience what it is like to be an auditor and how to receive an audit. 

This seminar will include overviews of the various regulations that affect laboratories and understand how they drive the audit, including 21CFR Part 11 as so many modern laboratories rely on computer-based data acquisition and reporting. We will provide forms and templates used in conducting audits, and train on when and how to utilize these tools. Each participant will write an audit observation as an auditor, and separately respond as an auditee to an observation and design a corrective action plan. We will explore all the aspects of laboratory operations including test methods validation, notebooks, instrument and equipment qualification, training records and data systems that are subject to audit. 

You will leave these two days of training ready to receive an inspection with confidence in your new skills. You will be better prepared than ever before to be part of a less stressful audit with fewer observations.

Learning Objectives:

  • Be prepared to receive both internal and external audits.
  • Reduce the anxiety, costs and observations of audits.
  • Know what to say and show, and what Not to say and show.
  • Understand how auditors think and what they are looking for.
  • Write responses, audit observations, corrective actions and remediation plans.
  • Learn the best practices for test method validation, instrument qualification and data system validation to avoid observations (“483s”).
  • Know when to do what to meet audit requirements economically.
  • Have the answers to the auditors' questions.

 

Who will Benefit:

  • Laboratory Managers
  • Quality Assurance
  • Quality Control
  • Laboratory Analysts/Chemists
  • Analytical Development
  • Regulatory Compliance
  • Contract Laboratories
  • Contract Research Organizations
  • Contract Manufacturing Organizations
  • Auditors

 

For Registration -   http://www.complianceonline.com/laboratory-inspections-internal-and-external-audits-seminar-training-80038SEM-prdsm?channel=pickevent


Note: Use coupon code 232082 and get 10% off on registration.

Join the conversation

Upcoming events

Risk Based Internal Auditing (RBIA): 2-day Comprehensive Training Workshop

l1 Jun 15 | 8:30

Course Description: Risk Based Internal Auditing (RBIA) is defined by the...

Q

Quality Control Laboratory Compliance - cGMPs and GLPs: One and a Half-day In-person Seminar

l2 Jun 15 | 8:30

Course Description: FDA inspection and oversight of quality control (QC)...

Q

Human Resources and Employment Law Essentials: 2-Day In-Person Seminar

l4 Jun 15 | 8:30

Course Description: Is your company at risk for non-compliance? Is your...

Q

Managing an Effective AML Compliance Program: 2-day In-Person Seminar

l4 Jun 15 | 8:30

Course Description: Are the financial transactions within your organization...

Q

Essentials of ERM and Assessing its Effectiveness Using ISO 31000

l4 Jun 15 | 8:30

Course Description: If an internal audit is to assess the effectiveness of the...

Q

Essentials Of USP Microbiology - Reading Between the Lines of the USP General

l8 Jun 15 | 8:30

Course Description: The objective of this two day "Essentials of USP...

Q

FDA's Medical Device Software Regulation Strategy: 2-Day In-Person Seminar by Ex-FDA Official

l9 Jun 15 | 8:30

Course Description: The growth of the medical software industry outpaces the...

Q

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

l11 Jun 15 | 8:30

Course Description: Raw material requirements in a cGMP environment are often...

Q

Post-Market Compliance for Medical Devices and Evolving Reporting Requirements

l11 Jun 15 | 8:30

Course Description: This interactive one and a half day course led by Ms. Rita...

Q

Auditing the Human Resource Function & Human Resource Metrics: 2-day In-person Seminar

l11 Jun 15 | 8:30

Course Description: This seminar will cover auditing human resources practices...

Q

FDA's New Import Program Concerning International Consequences: 2-day In-person Seminar

l11 Jun 15 | 8:30

Course Description: Importing products regulated by the FDA has become more...

Q

Internal Control Best Practices for your Procure to Pay (P2P) Process

l11 Jun 15 | 8:30

Course Description: This two day seminar will focus on internal controls...

Q

Detecting and Preventing Internal and External Fraud: 2-day In-person Seminar

l18 Jun 15 | 8:30

Course Description: Organizations of all kinds and sizes are increasingly...

Q

SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations

l18 Jun 15 | 8:30

Course Description: Formal written Standard Operating Procedures (SOPs) are...

Q

Building a Vendor Qualification Program for FDA Regulated Industries

l18 Jun 15 | 8:30

Course Description: If you are looking for the answer to the following...

Q

Regulatory Compliance for Dietary Supplements in the US, EU and Canada: 2-day In-person Seminar

l25 Jun 15 | 8:30

Course Description: A growing public demand for supplements has resulted in a...

Q

Computer System Validation - Reduce Costs and Avoid 483s: 2-day In-person Seminar

l25 Jun 15 | 8:30

Course Description: Significant changes in the regulations and...

Q

21 CFR Part 11 Compliance for SaaS/Cloud Applications: 2-day In-person Seminar

l25 Jun 15 | 8:30

Course Description: Significant changes in the regulations and industry...

Q

Supplier Management for Medical Device Manufacturers

l25 Jun 15 | 8:30

Course Description: Supplier selection and management is one of the critical...

Q

Import Procedures and Documentation

l25 Jun 15 | 8:30

Course Description: This 2-day seminar is designed to assist companies that...

Q

Project Management in Human Resources: 2-Day In-Person Seminar

l25 Jun 15 | 8:30

Course Description: Naturally, getting a project to deliver on time, within...

Q

The European Clinical Trial Directive…Plus…European Filings and Registration Procedures

l25 Jun 15 | 8:30

Course Description: This interactive two day seminar will cover the various...

Q

Compliance Processes for Life Science Products in Brazil, Russia, India, China markets

l9 Jul 15 | 8:30

Course Description: This seminar will help you understand the regulatory,...

Q

Technical and Regulatory Writing for FDA Regulated Industries

l9 Jul 15 | 8:30

Course Description: Regulatory professionals have to write highly technical...

Q

Operations Risk Management and Mitigation - from Assessment to Implementation

l16 Jul 15 | 8:30

Aims Recently, a series of headline-grabbing operational risk incidents at...

Q

How to get a CLIA Waiver for your Medical Device: One and a Half Day In-person Seminar

l16 Jul 15 | 8:30

Course Description: FDA has granted precious few applications for waiver since...

Q

Lifecycle Approach to Analytical Methods for Drug Products

l16 Jul 15 | 8:30

Course Description: This highly interactive course is designed to provide...

Q

How to Successfully Manage an FDA High Risk Food Inspection

l16 Jul 15 | 8:30

Course Description: This course will present an overview of necessary actions...

Q

Practical Considerations for Conducting FDA-Required Regulated Studies

l16 Jul 15 | 8:30

Course Description: Studies of veterinary drugs are required to be conducted...

Q

Aseptic Processing Challenges

l16 Jul 15 | 8:30

Course Description: The manufacture of aseptically produced sterile products...

Q

OCEG approved GRC (Governance, Risk and Compliance) Professional Seminar

l16 Jul 15 | 8:30

Course Description: This GRC Professional Seminar will teach you how to...

Q

GMP Compliance for Quality Control and Contract Laboratories: 2-day In-person Seminar

l27 Jul 15 | 8:30

Course Description: Quality control and related contract laboratories are...

Q

Analytical Instrument Qualification and System Validation: 2- day In-person Seminar

l30 Jul 15 | 8:30

Course Description: Analytical instruments should be qualified and systems...

Q

Validation, Verification and Transfer of Analytical Methods

l4 Aug 15 | 8:30

Course Description: Analytical methods and procedures should be validated to...

Q

Identity Theft Exposure and the Methods Utilized to Prevent

l5 Aug 15 | 8:30

Course Description: This course will highlight the need for all businesses to...

Q

Manufacturing and Marketing Cosmeceutical* and Homeopathic OTCs

l6 Aug 15 | 8:30

Course Description: This interactive one and a half day seminar is intended to...

Q

Fraud Evaluation Tools for the Internal Auditor

l6 Aug 15 | 8:30

Course Description: The topic of fraud — whether it relates to awareness and...

Q

Implementing a Basel III and COSO Compliant Operational Risk

l6 Aug 15 | 8:30

Course Description: Recent scandals as well as legal and regulatory actions...

Q

Anti-Corruption Compliance - Understanding the OECD Anti-Bribery Convention

l26 Aug 15 | 8:30

Course Description: Bribery can often damage your business and your...

Q

Why is FDA at my facility, and what do I do during an inspection?: 2-day In-person Seminar

l8 Oct 15 | 8:30

Course Description: This two day course will prepare firms for a quick,...

Q

Regulatory Crisis Management: Best Practices for Dealing with the Common Crisis Events

l12 Nov 15 | 8:30

Course Description: Unlike risk management, which involves managing potential...

Q