Regulatory affairs assess and perform quality checks to ensure that the medicinal drugs are safe and effective for consumer. Regulatory affairs also important to protect the pharma company from any liabilities of negligence.
We support organizations to understand the requirements of Regulatory bodies for all international supplies and manufacturing practices, documentation of clinical findings, scientific data and all other records. Making Business Processes and system all time readiness for any un announced inspection / audits by regulatory bodies.
It covers from Raw material to finish products to final packaging.
Our team closely work in the area of Technical report writing, Data Integrity, Inspection readiness and all such areas.
