Makrocare specializes in Regulatory, Clinical and Post-Marketing services and solutions to the medical device and diagnostics industry. Our team of regulatory and clinical experts ensures your clinical evidence, labeling and regulatory falls in compliance with new MDR/IVDR regulations. MakroCare for 15+ years has been successfully helping many Medical Device companies right from designing their Regulatory Strategy to getting product approvals globally across North America, Europe, and rest of the world with detailed knowledge of different local submission processes.
For more details log on to www.makrocare.com.
At this time, there are a variety of sponsorship and exhibition opportunities available for companies wishing to increase their visibility and participation in the program, ranging from keynote speaking opportunities through to exhibitor and documentation sponsors. Organizations most suitable for this type of exposure provide services and solutions including:
- European Regulatory Affairs Specialists
- International Regulatory Consultants
- Clinical Research Organizations
- eLabeling & UDI Technology Specialists
- Quality Assurance Software Providers
- Legal Firms
MedBoard organizes Medical Device information, making it quickly accessible, integrated, actionable and useful, and creates the tools that medical device companies and professionals need. Covering 60+ countries, including regulations, guidance, latest news, standards, definitions, surveillance of market data and much more; all integrated into a unique algorithm and smart search engine which provides relevant results taking the user to the information needed. MedBoard is used by leading organizations and is an essential product for today’s executive.