Vittarthaa has been actively preparing cleaning validation documents since 2017, that are critical safety reports of GMP and Quality Assurance. The assessment of all the documents is performed by a team of experienced Toxicologists. Several documents have been submitted, reviewed, and constantly scrutinized by various clients for their regulatory inspections, such as USFDA, MHRA, etc. Currently, Vittarthaa provides services for various manufacturing units that have cGMP facilities to prevent possible contamination and cross-contamination of APIs and finished products. All the documents generated at Vittarthaa are thoroughly reviewed and identified to be easily traceable and retrievable. Vittarthaa’s cleaning validation document assures audit readiness, cleaning programs, and direct use in the facility and after-reporting services to clarify and support during any inspection and any other activity as required.