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MakroCare has successfully assisted many Pharma, Biotech and Device companies' right from designing their Regulatory Strategy to getting product approvals globally.We have been managing more than 4000 Regulatory submissions (Clinical,Market Authorization and Post Market Maintenance Applications) annually. Our functional services include CMC Authoring, Clinical Authoring, LCM, Labeling & Submission Management. Meet our team in RAPS for all your Regulatory queries.
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