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Submission Management

Global regulatory differences and constant changes in country submission requirements is a challenge to Regulatory Operations teams for proper submission planning and execution.

MakroCare, over the years, has established flexible methodology and infrastructure, for fast and effective global submissions to Health Authorities globally. Whether they are CMC applications, market authorization applications or life cycle management, MakroCare is managing submissions in more than 100 countries. Our teams are connected to deliver integrated services across North America, Europe, Asia, and ROW with detailed knowledge of different local submission processes.

MakroCare through its Subsure supports clients in:

  • Bullet Managing Global Submissions
  • Bullet Assess the impact of proposed changes in terms of countries impacted, ongoing regulatory procedures, resources required
  • Bullet Coordinate with manufacturing sites and Regional Regulatory teams on regional data/requirements
  • Bullet Cross-function, cross-country and cross-vendor coordination for required information
  • Bullet Create review for Regulatory submission content for all the submissions
  • Bullet Author HA compliant Dossiers
  • Bullet Liaise with Health Authorities
  • BulletSubmission and Approval

Through our shared resources and management techniques, MakroCare offers innovative value-added services which will help Regulatory teams in getting the scale in shortest possible time to manage uneven loads and ever-changing Regulatory requirements

The First Step

Let's talk about how MakroCare can help you