Planetary Defense

Planetary Defense encompasses a broad range of activities led by national and international space agencies, academic institutions, and policy stakeholders. The field focuses on protecting Earth from potential hazards posed by near-Earth objects (NEOs), such as asteroids and comets. Key components include the discovery and ongoing characterization of these objects, the development of impact mitigation strategies, and the implementation of early warning systems and impact risk assessments.

Our company offers expert consulting services in support of these efforts by providing a highly educated and experienced workforce at the PhD level and GSA level 13 and 14 expertise. Our team members have worked directly with leading institutions such as NASA, ESA, and the IAU Minor Planet Center, and bring with them a strong track record of publishing scientific results in peer-reviewed journals. We offer 24/7 support from strategic time zones, including GMT, to ensure continuous global coverage.

We bring deep technical expertise in:

• Celestial Mechanics and Astrodynamics

• Programming and Scientific Code Development in Python

• Relational Database Design, Maintenance, and Administration (MySQL, PostgreSQL)

• Software Development on Unix/Linux Platforms

• Project Management Tools (including JIRA)

• Technical Customer Support and Scientific Communication

Through this combination of scientific rigor, software engineering, and operational experience, we are well-positioned to support planetary defense projects across research, data processing, survey simulations, and mission support.

Our company provides specialized consulting services in the field of medical device regulations. Navigating the complex and ever-evolving regulatory landscape is essential for ensuring market access, compliance, and patient safety across global markets.

We support companies in fulfilling a wide range of regulatory functions, including:

• Internal Audits for compliance readiness and process improvement

• Regulatory Strategy and Compliance for the EU (MDR/IVDR), USA (FDA), and other international markets

• Product Registration and Submissions

• Document Control Systems

• Training Management Programs to ensure regulatory and quality system awareness across teams

• Preparation and Handling of Notarized Documents, including authentication and apostille processes for international legal recognition

Our experience ensures that clients are equipped with both the regulatory knowledge and practical tools to bring products to market efficiently while meeting local and global compliance standards.

Medical Devices Regulations