Regulatory Submissions
TATTWA Consultants streamlines your regulatory submissions, ensuring timely product approvals across MedTech, Pharma, Ayurvedic, Nutraceutical, and Cosmetic sectors. We specialise in preparing high-quality Technical Documents that meet the standards of CDSCO, USFDA, EMA, and other global regulatory bodies.
Our end-to-end service includes data review, validation, gap analysis, dossier compilation, and final submission. With deep knowledge of regulatory requirements, we ensure every submission is accurate, compliant, and audit-ready.
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We also manage post-submission activities like responding to queries, deficiency letters, and handling renewals or modifications. Whether it’s device registration, drug approval, or nutraceutical licensing, we help you avoid delays or rejections by ensuring submission excellence.
Partnering with TATTWA means leveraging regulatory documentation as a strategic asset. Our experienced team transforms complex requirements into a smooth, predictable submission process, helping you get your product to market faster and with full confidence in your regulatory compliance.