Our Partners
To further our mission of providing the highest quality of service to our clients, we have created collaborations with several other companies who uphold the same standards of excellence and ethics and are able to supplement our expertise, capacity and service offerings. Through these collaborative agreements we are able to provide superior service to our clients worldwide. We proudly display our partners below:
The Cascadia Drug Development Group (CDDG; www.thecddg.com) is a Pacific Northwest-based consulting and drug development group that offers a wide range of expertise within an integrated framework. CDDG was founded by seasoned industry experts who are passionate about drug discovery and whose mission is to elaborate a new virtual model for therapeutic development.
CDDG can provide strategic oversight of drug development, from discovery to early clinical development. The founders have a strong scientific background in immunology and support a number of therapeutic areas, including inflammatory and autoimmune disease, infectious disease, metabolic disease and oncology. Through their network of vetted affiliates, they offer subject matter expertise in such areas as toxicology, PKDM, biomarkers, regulatory and patent law and early clinical operations. CDDG utilizes a flexible and virtual structure, which allows them to adapt to client needs and reduce overall costs. Their operating model is well-suited to highly interactive and efficient de-risking of projects and maximizing the value of client programs.
FlexPoint Bio (www.flexpointbio.com) is a specialized consulting firm that supports small to mid-sized biotechnology companies in advancing clinical development through expert guidance in biomarker strategy, biospecimen logistics, vendor selection and oversight, and AI integration.
Their mission is to bridge the gap between scientific innovation and operational execution - enabling clinical teams to deliver high-quality, inspection-ready data while accelerating study timelines. With extensive expertise in biomarker and biospecimen management, the company provides end-to-end solutions, including biomarker selection and operationalization, data flow optimization, regulatory-compliant documentation, and full biosample lifecycle planning. In the area of clinical outsourcing, the firm provides strategic support through the development of fit-for-purpose vendor engagement models, targeted CRO and third-party vendor selection, vendor governance frameworks, and proactive risk mitigation strategies.
The company also guides AI adoption within the clinical development environment. Services include infrastructure readiness assessments, vendor-agnostic provider selection, and ongoing performance monitoring to ensure AI tools align with compliance, efficiency, and outcome-driven goals.
Dahlia Consulting (www.dahlia-consulting.com) was founded in 2014 to provide consulting services to the life science industry bringing together a group of professionals in the area of Program, Projects and Portfolio Management in order to bring structure to company strategy and translate goals to operational activities, execution and continuous improvements with focus in the Biopharma, Cell & Gene Therapy start up’s companies, as well as remediations for Biologics and Vaccines.
Since its foundation, Dahlia has expanded its capabilities and services globally (US, EU and China) in the following areas: Quality & Compliance, GXP & Regulatory, Quality Management Systems, Regulatory Compliance, Pre-Approval Inspections, CMC , Technical writing, Vendor/ Supplier Quality Audits, Validation, Supply Chain, Information Technology & Security, Resource Planning, Staff Augmentation, Talent Sourcing, Personal / Coaching Development and Market Access & Reimbursement.
With a proven track record of 43 successful GMP projects in the last 24 months, cGMPnow (www.cgmpnow.com) delivers Turnkey GMP Systems that accelerate Next Generation Therapies to patients. Our expertise spans GMP facility due diligence, design, and regulatory compliance, enabling us to provide turnkey systems, from streamlined equipment procurement and automation to full facility validation. We specialize in both greenfield builds and renovations, ensuring cost-effective and rapid pathways to GMP manufacturing.
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The names and Logos displayed are Trademarks of the respective companies.