MakroCare Exhibits at Asia Regulatory Conference 2013, Singapore

Meet MakroCare, an International Development and Commercialization services firm at Asia Regulatory Conference 2013, Singapore

Newark, NJ (I-Newswire) January 18, 2013 - Meet MakroCare, one of the sponsors of the Asia Regulatory Conference 2013 held at Raffles Convention Centre, Singapore on 28-30 January, 2013.

Asia Regulatory Conference 2013 offers a unique opportunity for key stakeholders from health authorities, local and multinational pharmaceutical companies, and clinical research to meet and exchange views, discuss topics of interest and identify focus areas for ongoing efforts to increase patient access to new and improved medicines.

This conference will provide a forum to:

•Facilitate discussion on common issues in the regulatory and technical areas in Asia
•Encourage greater convergence of regulatory requirements in Asia
•Strengthen cooperation between Asian regulatory authorities and pharmaceutical industry

Conference speakers will include top-level regulatory authorities from several Asian countries as well as leading experts in the ICH process. In addition, speakers will include representatives of WHO, various regulatory agencies from other regions and the multinational and local pharmaceutical industry.

MakroCare is sponsoring and exhibiting, Visitors/Delegates are welcome to visit us in Asia Regulatory Conference 2013, Singapore, to know more about our Regulatory, Quality & Risk Management Services.

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.