Principles of cGMP in Pharmaceutical Industry Skills Course

"Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product." ("GMP question and answers." n.d.)

Why You Need to Take This Training Course?

This course will Let YOU:

  • Understand the safety and efficacy of medications: cGMP regulations are designed to ensure that medications are manufactured in a way that is consistent, safe, and effective. By following cGMP regulations, you can help to prevent contamination, errors, and other problems that could lead to unsafe or ineffective medications.

  • Protect your company from regulatory action: The FDA and other regulatory agencies take cGMP compliance very seriously. If your company is found to be out of compliance with cGMP regulations, you could face fines, product recalls, and even criminal charges. Taking cGMP training can help you to avoid these problems.
  • Understand the importance of quality control procedures
  • Learn how to identify and prevent potential problems
  • Develop a strong understanding of regulatory requirements
  • Stay up-to-date on the latest cGMP regulations
This article offers free shipping on qualified Face mask products, or buy online and pick up in store today at Medical Department.

What you'll learn

  • The participants will have the basic knowledge of what is GMP. They will know what is Quality Management and the requirements for a quality assurance unit
  • The participants will be able to review measures to ensure good sanitation in premises, personnel, equipment, apparatus and more..
  • The participants will understand the basic aspects of qualification and validation & its scope
  • The participants will conceptualize complaint handling procedures and product recall procedures
  • The participants will have the basic knowledge on the general issues that arise when considering contract manufacture or analysis
  • The participants will realize the general issues related to requirements & training for key personnel
  • The participants will identify the role of self-inspection in the quality management system
  • The participants will know the key requirements for site choice and the specific requirements for main areas and many more
Instructor: Dr. Samer Sowidan
Register in this Course

This 15-hour Training Course is Equivalent to 13 Continuing Professional Development (CPD) hours.

  • Duration: 15 Hrs. Two Days
  • Time: 9.00 am-5.00 pm
  • Prerequisite for this course: None
  • Language: English
  • Level: Management or any one interested
  • Classroom or Vitual Training
  • Price US $ 495
  • Certified and Accredited Certificate
  • Discount available for companies who send three or more participants
  • Seats for this course: 12
  • Virtual through google meet
  • Classroom course at Upbeat office, hotel or at the customer premises ​

Registration Form ​

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