Course Description

Understanding GMP requirements, refreshed on a yearly basis is critical to maintain high-GMP standards in your company. Knowledge and skill surrounding the application and practice of GMPs is fundamental to avoiding regulatory issues. It’s simple – you have to do it and you and your team must comply. You cannot assume that once taught, the content associated with GMPs will be retained from year to year. As human beings, we tend to forget over time and as we forget, we also get careless. In the health sciences there is no margin for error or tolerance for carelessness. This training will provide foundation to your GMP training.  


Training Agenda 2 Days

Each Day Session start time 12:00 PM EDT

GMPs – Government Regulations

  • What are the regulations governing Good Manufacturing Practices?
  • Your responsibilities
  • Pertinent GMP topics as per the code of Federal Regulations
  • ­Quality Management
  • ­ Personnel 
  • ­ Premises and equipment
  • ­ Documentation
  • ­ Production
  • ­ Quality Assurance
  • ­ Materials management
  • ­ Production and in-process controls
  • ­ Packaging and labeling
  • ­ Storage and distribution
  • ­ Laboratory controls
  • ­ Validation
  • ­ Change control
  • ­ Rejection and re-use of material
  • ­ Complaints and recalls
  • ­ Supplier controls

GMP Inspections

  • Preparing for a GMP Inspection
  • The consequences of not being ready
  • The specific areas that are inspected during a GMP inspection 

FDA Inspection Tips and Recommendations

  • The FDA Inspection – how is it structured and conducted
  • Responding and organizing for the FDA Inspection
  • Importance of truthfulness
  • knowledgeability and confidence
  • FDA Tricks to elicit information
  • Arguing and challenging
  • Behavior during the inspection
  • Importance and role of documentation
  • Effective communication skills
  • Being deceptive
  • Opinion versus fact
  • Phrases never to say
  • Handling adverse findings during the inspection

Summarise

  • Questions & Answers with Faculty
  • New GMP Topics
  • Many Case Studies
  • Certificate Awarded to all the attendees

Each Day Session End Time 04:00 PM EDT


Who will Benefit

  • Virtually everyone in the health sciences, everyone within the organisation, can benefit and in most cases, is required to attend periodic GMP training.
  • Compliance
  • Quality
  • Marketing
  • Engineering
  • Operations

Course Background

CGMPs or Current Good Manufacturing Practices is a general encompassing term for the regulations that the control of all facets of life sciences manufacturing processes and facilities particularly pharmaceutical products.

 It is crucial, for any entity to be compliant, that every individual within the organization fully understand and adhere to these regulations in the course of Adherence to those regulations assures the identity, strength, quality, and purity of drug products by requiring that manufacturers of medications adequately control manufacturing operations. This includes establishing strong quality management systems, obtaining appropriate quality raw materials, establishing robust operating procedures, detecting and investigating product quality deviations, and maintaining reliable testing laboratories. This formal system of controls if adequately put into practice, helps to prevent instances of contamination, mix-ups, deviations, failures, and errors. This assures that drug and medical device products meet their quality standards.

The CGMP requirements were established to be flexible in order to allow each manufacturer to decide individually how to best implement the necessary controls by using scientifically sound design, processing methods, and testing procedures. The flexibility in these regulations allows companies to use modern technologies and innovative approaches to achieve higher quality through continual improvement. Accordingly, the "C" in CGMP stands for "current," requiring companies to use technologies and systems that are up-to-date in order to comply with the regulations. Systems and equipment that may have been "top-of-the-line" to prevent contamination, mix-ups, and errors 10 or 20 years ago are less than adequate by today's standards.

It is important to note that CGMPs are minimum requirements. Many manufacturers are already implementing comprehensive, modern quality systems and risk management approaches that exceed these minimum standards.

Choose a Purchase Option


$1,295

One Dial-in One Attendee - Live 2 Day Virtual Seminar

Early Bird $1295 Regular Price $1985

You get one log-in for the live virtual seminar for one participant, presentation materials , Certificate and the opportunity to ask questions by phone and email.

$1,496

Recorded Access Single Participant

12 Hour Virtual Seminar

You'll have 6 month access to single log-in for an archived recording of the entire 12 Hour virtual seminar including the Q&A period. You can log in any time of day or night. You'll also receive all presentation materials, plus an audio recording and transcript for the entire session. Delivery is approximately 48 hours after the session

$4,995

Group-Max. 10 Attendees - Live + 12 month Access

12 Hour Virtual Seminar

You get Group log-in for the live virtual seminar for 10 participants, presentation materials , Certificate and the opportunity to ask questions by phone and email. On Demand Recorded Access is Included for 12 months for the Group.

$4,998

Recorded Access Group-Max. 10 Attendees

12 Hour Virtual Seminar

You'll have 12 month access to group log-in upto 10 attendees for an archived recording of the entire 12 Hour virtual seminar including the Q&A period. You can log in any time of day or night. You'll also receive all presentation materials, plus an audio recording and transcript for the entire session. Delivery is approximately 48 hours after the session

FDA Faculty Charles H. Paul

Faculty Charles H. Paul 

President at C. H. Paul Consulting LLC

Tobyhanna, Pennsylvania, United States

Charles H. Paul is the President of C. H. Paul Consulting, Inc. – a regulatory, training, and technical documentation consulting firm. Charles is a management consultant, instructional designer and regulatory consultant and has led C. H. Paul Consulting, Inc. since its inception over 25 years ago. He regularly consults with Fortune 500 pharmaceutical, medical device, and biotechnology firms assisting them in achieving human resource, regulatory, and operational excellence. He is a regular presenter of webinars and on-site seminars in a variety of related subjects from documentation development to establishing compliant preventive maintenance systems.

The firm works globally completing projects throughout the EU, UK, South America, and Asia.

Our Past Seminar Testimonial


The presentation by Carolyn Troiana today was fantastic, both I and the QA Manager (Aaron Neighbour) loved it and had extensive conversation afterward about it. ( FDA Compliance and Mobile Applications Webinar )

Robert Friedland ( IT Manager) NUTEK BRAVO, LLC.

Thank you for providing the information in such detail. It was helpful to gain the perspective of somebody that has implemented these regulations in a working lab. Virtual Seminar on ( Training on Life cycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines )

Tracey Kessler ( Director of R&D) CEL-SCI Corporation

I felt the seminar was very helpful and provided good insight for DataIntegrity and what the FDA is looking for per the regulations. ( Current Regulatory Thinking on Data Integrity 2 Days Virtual Seminar )

Margaret A. Clifton ( Manager, Quality Systems) CSL Plasma

The presenters subject matter knowledge is extensive which enables information to be shared in detail. (Training Attended on Risk Based Verification and Validation Planning to Meed US FDA and ISO 13485 Requirements )

Stuart Chisholm (Sr. Principal Device Engineer) Teva Pharmaceuticals

About World Compliance Seminars (WCS)

World Compliance Seminars (WCS) is one stop solution for all your pharmaceuticalbiotechnology and medical device certification program needs. The pharmaceutical and medical device training requirements are set forth by the FDA (Food and Drug Administration) and other major regulatory bodies like NIHEMA, as well as numerous European based national regulatory bodies.

These requirements are important to the training of pharmaceutical reps who are responsible for the education, professional development, and on-the-job training. The training is broken down into different sections to cover a wide variety of topics, including pharmaceutical formulation, pharmaceutical transfer processes , GLP, GMP, Clinical ComplianceProcess Validation, Global Regulatory Affairs, Document Management,GMP (Good manufacturing practice) QSR and CMC and many more.

The pharmaceutical and medical device requirements that the FDA has set forth are designed to protect the public's health and safety. Pharmaceutical reps must adhere to all of the regulations and education courses provided by the FDA in order to be considered one of the best in their field. They also must complete ongoing educational opportunities and maintenance programs in order to maintain relevance and career enhancement.

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