Comprehensive Support for Your R&D Needs

Our Services

Cronet provides unique and focused approaches to make preclinical studies become a success appling a rigourous scientific method at all levels of the project, starting from the regulatory compliance up to all aspects of in vitro and in vivo study.

Regulatory Consulting

Navigating the regulatory landscape can be complex. We help you stay compliant and accelerate approvals with:

  • Regulatory strategy development – Crafting tailored roadmaps for successful submissions.
  • Document submission, preparation, and compliance – Ensuring adherence to international regulatory requirements.
  • Liaison with health authorities – Facilitating clear and effective communication with regulatory agencies.

Scientific Support

Scientific rigor and method are the core of successful R&D. Our team provides:

  • Preclinical study design and management – Structuring studies for meaningful, regulatory-compliant results.
  • Data analysis and interpretation – Turning raw data into actionable insights
  • Scientific writing and documentation – Producing high-quality reports, white papers, and regulatory documents.

Project Management

Efficient project execution requires strategic coordination. We offer:

  • End-to-end project coordination – Managing all phases from concept to completion.
  • Risk assessment and mitigation – Identifying challenges and implementing proactive solutions.
  • Timelines and resource optimization – Ensuring projects stay on track and within budget.

Pharmaceuticals

Regulatory

Non clinical

Risk assessment

Analytical and Bioanalytical

Imaging

Medical devices

Biological Safety

Performance Evaluation

Technical Documentation

Quality ISO 13485

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Others

Glp Quality

Safety Assessment of Food Products and Additives