Visit MakroCare at Booth T6 & T7 in RAPS Regulatory Convergence, San Jose, CA on 17-20 September

RAPS Regulatory Convergence is the premier event for regulatory professionals working in the medical device, pharmaceutical and biotech industries. In addition to working in submission and

compliance, play integral roles in every stage of the lifescience product lifecycle including development, distribution, marketing and post-market surveillance.

With over 15 years of rich experience, MakroCare is helping clients in solving the Regulatory puzzle with innovative and customised solutions. We have a strong team of dedicated professionals

with many years of industry and agency experience, who can tailor project plans to meet your regulatory requirements. We have built a successful track record of timely and extensive approvals.

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.