RAPS: This course has been pre-approved by RAPS as eligible for up to 3.0 credits towards a participant's RAC recertification upon full completion.
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. Get to know more about this seminar in the following sections.
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.
Curious to know the agenda of this seminar? Here is the list for you!
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. Get to know more about this seminar in the following sections.
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
Curious to know the agenda of this seminar? Here is the list for you!
Course Content
Session 1: U.S., EU, and Japan GMPs - Status of Harmonization& Future Trends
Session 2: APIs
Session 3: Area GMP Inspections
Course Provider
Kelly Thomas,
Who Should Attend
No matter how new you are to the industry, pharmaceutical GMP training will help you deliver the best possible work.To further clarify the relevance of cGMP online training for professionals, here is a list of beneficiaries:
- R&D Associates and Research Scholars: Helps you understand the basic laboratory norms and pass the FDA GMP inspection with the best ratings.
- IT Subject Matter Experts: Makes you thorough with production facility protocols, equipment, tools, and machines. This guarantees better execution of technical knowledge by adhering to standard norms.
- Contract Laboratories: Empowers lab technicians with the knowledge of handling and storage of raw materials, sanitation and hygiene, quality control, and structuring of the lab.
- Regulatory affairs personnel: Gives you a standard manual to audit or investigate the laboratories and production units. Furthermore, allows you to conduct a thorough inspection at reputed laboratories.
- Senior Management: Provides you with a handbook of FDA GMP inspection checklist to observe the operations. You can also interrupt or change an SOP to improve the quality of the final product.
