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Cleaning Validation:  A Practical Approach
Cleaning Validation:  A Practical Approach
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Cleaning Validation: A Practical Approach

21 Oct 2022 - 22 Oct 2022
Free Registration

Event Details

Cleaning Validation: A Practical Approach

Pharmaceutical Manufacturers have to consistently achieve a high standard of product quality. A well-planned and effective cleaning process plays a very important role in this by eliminating contamination & cross-contamination. A documented evidence is required to prove that the cleaning methods in place are consistent and in line with cGMP requirements. Ineffective cleaning processes can, not only lead to more batch failures but also result in FDA 483s and warning letters.
The last few years have seen the regulators increasing the amount of interest and scrutiny for cleaning validation during inspections. FDA inspectors now want to see a functioning cleaning validation program with appropriate documentation in place during their inspections. Let us try to understand where the gap lies, between the regulator's expectations and the pharma companies, which is leading to an increase in citations relating to cleaning validations.
Adoption of technology is currently picking up pace in the pharma industry, what tools are available for ensuring compliance related to cleaning validation.
Eminence Business Media, brings this open forum, "Cleaning Validation – A Practical Approach", where you can discuss your questions and get answers for the challenges that are faced by the teams and collectively implement the learnings

Entry Fees

Free Registration

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Event Frequency

One Time

Event Timings

(GMT+5:30) Mumbai, Kolkata, New Delhi
10:00 AM - 06:00 PM (Oct 21, Oct 22) (General)

Organizer

Eminence business media

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We at Eminence, aspire to pool our research and deliver it with the assistance of industry stalwarts. We believe that business growth is a 4 step process starting with Knowledge followed by Excellence and the resultant is Economic Development. By...

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Ramakrishna Goulikar
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