In an exceedingly interconnected and rapidly evolving regulatory space where new layers of complexities are omnipresent, our Regulatory Affairs experts provide strategic guidance and support to interface and comply with the various regulators. Our services include Regulatory Strategy and Planning, compliance, submission management and more.
Regulatory Strategy and Planning
- Develop tailored regulatory strategies that support product development and commercialization efforts.
- Identify regulatory requirements and potential roadblocks
- Identify regulatory requirements and potential roadblocks
- Create regulatory timelines and milestones.
- Prepare and review eCTD filings in the US, Canada, and The European Union to ensure local regulator’s requirements are met.
Regulatory Compliance
- Prepare various risk assessments as per FDA/EMA/ICH requirements
- Conduct regulatory gap analysis and implement corrective actions
- Provide training on regulatory requirements
Submission Management
- Assist you in preparing and submitting IND, NDA, BLA, and MAA with various regulatory agencies
- Assist you in managing and interacting with regulatory agencies
- Address Clarifaxes, comprehensive response letters and other agency requests
Labeling and Packaging Compliance
- Develop compliant labeling and packaging materials
- Review and update labeling and packaging to ensure regulatory compliance
- Ensure consistency across global markets
Regulatory Inspections and Audits
- Prepare clients for regulatory inspections
- Conduct mock audits ad provide remediation guidance
- Develop and implement corrective action plans
Regulatory Intelligence and Monitoring
- Track and analyze regulatory changes and updates
- Provide alerts and impact assessments
- Identify potential regulatory risks and opportunities
- Develop strategic responses to regulatory changes
Clients benefit from our expertise in the pharmaceutical, medical devices, vaccines, generic and biosimilar industries through:
- Expert guidance on regulatory requirements
- Increased efficiency in regulatory submissions
- Reduced risk of non-compliance
- Strategic planning for regulatory success
- Enhanced credibility with regulatory agencies