MakroCare Launches Vistaar - Regulatory Intelligence Tool

Online, July 31, 2013 (Newswire.com) - MakroCare today announced the addition of Vistaar, a Regulatory Intelligence tool, to it's RA portfolio. Reg Intel was always the foundation of MakroCare services, with Vistaar, it's formalized as a tool that it's customers can benefit from.

Vistaar will be part of Regulatory Affairs Center of Excellence (RACoE) that MakroCare formed earlier. Life Sciences customers can now leverage these assets of RACOE to their advantage to gain productivity and knowledge efficiencies.

This CoE currently supports Regulatory Operations, Life Cycle support, CMC/Clinical/Nonclinical Writing, Labeling, Regulatory BPO and Publishing for Global BioPharma. Regulatory Affairs teams at MakroCare also supports regulatory advisory and full service dossier management for sponsors.

Furthermore, the CoE team will bring pre-integrated service offerings and regulatory best practices to add value to client's processes for greater efficiency.

Makrocare is a global specialized consulting partner with extensive expertise in emerging region strategic design, regulatory compliance and governance, clinical, medical support and risk management planning. With operations and presence in US, UK, Europe & Asia, MakroCare is well positioned to meet the development & commercialization needs of life science industry globally.

About MakroCare:

MakroCare is an international drug development and commercialization services firm that is dedicated to efficient, high-level performance in combination with unparalleled client satisfaction supporting from USA, Europe and Asia. MakroCare has 5 subsidiaries/divisions - Consulting, CRO, SMO, DDi and Commercialization. MakroCare has teams positioned worldwide in these divisions supporting product life cycle management, regulatory affairs, risk management, regulatory compliance, trial management (clinical, late phase), monitoring, biometrics (CDM, EDC, Biostat, SAS programming), Medical Writing (Regulatory, Clinical), QA audits, Drug safety / Pharmacovigilance, Site management, Patient Recruitment, Informatics (EDC, CTMS, IVRS), Commercialization, and Marketing/Sales.