Visit MakroCare at Booth T10 & T11 in RAPS Regulatory Convergence, 9-12 September 2017, National Harbor, Maryland
MakroCare,a full Regulatory Affairs support service consulting in USA, Europe & APAC is participating in RAPS' Regulatory Convergence, National Harbor, Maryland on 9-12 September 2017. Visit the expert Regulatory team in RAPS' Regulatory Convergence 2017 at Booth T10 & T11.
- Salisbury, MD (1888PressRelease) September 08, 2017 - 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 16 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.
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