cGMP or current good manufacturing practices are not limited to product development and monitoring of the SOPs. Everything plays an essential role, starting from the design of the facility, the strength of the unit, and the purity of the components.
Do you have the proficiency to update cGMP to its core? You will, after attending this cGMP training! The core purpose of this seminar is to establish a robust idea of how the quality of active pharmaceutical ingredients.
Course Overview
Do you think a consumer will be able to assess the quality of the drug? This is difficult by just smelling, touching, or looking at the final product. Hence, you need thorough pharmaceutical GMP training to ensure every consumer receives high-quality drugs.
Since a basic cGMP course is not sufficient to ensure quality, the effort is to improve the overall conditions under which a pharmaceutical product is manufactured. As a result, you will see a dip in cGMP violations, and the operations will improve significantly.
As per FDA GMP inspection guidelines, here are some controls they focus on:
- Improving management systems
- Reliable testing of the samples, raw materials, and final products
- Developing strict operating procedures
- Consistent work on reducing the deviations
- Procuring quality raw materials
- Thorough investigations of the deviations
By adhering to this FDA GMP inspection checklist, you can avoid the most common quality failures in your manufacturing unit. The 58-page document on cGMP has excellent updates which will be discussed in this cGMP training.
People Also Ask
Q1 Does this cGMP training explain how FDA inspects a facility?
Yes. Since FDA GMP inspection checklist has a standard protocol, your faculty will discuss it thoroughly. In addition, this cGMP training will also guide you to produce failure reports strategically in your favor and get approval from inspectors. Most senior professionals who attended this cGMP course have managed to receive a green signal in the FDA GMP inspection.
Q2 Does this seminar help professionals from new companies learn about cGMPs?
Yes. This cGMP online training includes a detailed discussion of recent guidelines and regulation documents released by the FDA. You will also get to know what FDA currently expects from the companies and why. Additionally, your faculty will share multiple resources that will help you build a company that complies with cGMP regulations to the edge.
Q3 What if the company is found to be non-compliant with cGMP guidelines? Can senior managers and project associates get help from this seminar?
Yes. Your faculty will thoroughly discuss cGMP violations and their nature to make you understand why your company was non-compliant. The violations could be due to labeling failures or inefficiency in the manufacturing process. This seminar will give you a broader perspective to tackle this situation and improve the overall operation.
Course Content
Session 1:
Course Provider
Ms Kelly Thomas,
Vice President ,
Stallergenes GreerMs. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation.
Utilizing strategic thinking, risk based approaches, and Lean principles, she has demonstrated success in steering and managing complex projects within the pharmaceutical and medical device industries.
