• Internal and External Audits (e.g., Data Integrity assessments, GxP facility audits including central labs, IRBs, CROs, computer validation,
software vendors, hosted services, etc.)
• Sponsor audit program establishment and improvement consulting
• Training and process development support
• Cyber and Data Privacy assessments
• CAPA and Deviation Management
• GxP Procedural system establishment or improvement (e.g., globalization, FA harmonization, regional/local alignment, etc.)
• EDMS system set-up and utilization consulting
• Process development facilitation
• Strategic resource for high visibility initiatives
• Management level SMEs with extensive experience within drug development
• Central and remote monitoring
• Risk assessment
Crafting detailed SOPs that provide clear, step-by-step instructions to ensure consistency and compliance in your processes.
Creating thorough and accurate CSRs that detail the methodology, results, and conclusions of clinical trials.
Preparing precise and compliant regulatory submission documents to meet the stringent requirements of regulatory bodies.
Developing user-friendly manuals and guides that facilitate the effective use of complex technologies and systems.
Developing detailed project plans that outline objectives, timelines, resources, milestones, and metrics that matter.
Identifying potential risks and implementing strategies to mitigate them, ensuring the smooth progression of projects.
Allocating and managing resources effectively to optimize productivity and efficiency.
Monitoring project budgets to ensure that all expenditures are within the allocated budget and identifying cost-saving opportunities.
Maintaining high standards of quality throughout the project lifecycle, ensuring that deliverables meet regulatory and industry standards.
• Conducting thorough research on relevant regulations such as CTR, Diversity Action Plans, and ICHE6R3.
• Providing clear and actionable interpretations to ensure compliance.
• Assisting with the implementation of regulatory requirements within your organization.
• Tailored Solutions: Developing customized change management strategies that are aligned with your corporate cultural vision.
• Communications: Crafting effective communication plans to ensure all stakeholders are informed and engaged throughout the change process.
• Training Development and Implementation: Designing and delivering training programs to equip teams with the skills and knowledge needed to embrace and sustain change.
We begin with a comprehensive consultation to understand your unique challenges, goals, and requirements in the clinical trial process. Our team takes the time to learn about your organization’s needs, ensuring a clear alignment on objectives and identifying the key areas where our expertise can make the greatest impact.
Based on the insights gathered, we develop a tailored plan that addresses your specific needs—whether it’s refining management processes, enhancing hiring practices, or supporting patent filings.
From managing daily processes to guiding you through complex regulatory requirements, we execute with precision and agility, adapting as needed to ensure your project stays on track and aligned with your goals.
Reach out to our dedicated team for any inquiries, appointment scheduling, or support.