CLEANING VALIDATION BLUEPRINT

COURSE DETAILS:

✅The "Cleaning Validation Blueprint" course provides a comprehensive overview of cleaning validation in the pharmaceutical industry, starting from its historical background to advanced validation techniques and regulatory compliance.

✅It begins with an exploration of the history and processes of cleaning validation, introducing key concepts such as cleaning levels, the bracketing approach, and worst-case scenarios. Central to the course is the detailed instruction on calculating and finalizing MACO, with a special emphasis on integrating Health-Based Exposure Limits (HBEL) for precision.

✅Participants will gain insights into effective sampling methods, including swab and rinse techniques, and how to set appropriate limits for both. The course tackles the challenge of cleaning the "Most Difficult to Clean" equipment using a lowest limit approach and differentiates between direct and indirect testing methods for cleaning verification.

✅It also addresses regulatory aspects, specifically FDA 483 findings related to cleaning validation, and offers practical training on swab method validation and glassware cleaning validation.

✅Concluding with a focus on career preparation, the course covers important interview questions in the field. This condensed program is ideal for professionals in quality assurance, control, analytical research, formulation research, and pharmaceutical manufacturing, aiming to equip them with comprehensive skills for executing and managing cleaning validation effectively.

Receive a certificate upon successfully finishing this course

DURATION: ⏳433 Minutes (7.21 Hours)

LANGUAGE: English

Offered as an online course featuring pre-recorded videos and structured for distance learning, this program is available to participants globally.

You will have lifetime access to the course