Subcontractors
Join SXR Laboratories’ trusted network of subcontractors and contribute your
specialized expertise to advancing clinical research across diverse therapeutic areas.
SXR Labs
📞 020 3148 8876 ✉️ support@sxrlabs.com
SXR Labs
📞 020 3148 8876 ✉️ support@sxrlabs.com
Join SXR Laboratories’ trusted network of subcontractors and contribute your
specialized expertise to advancing clinical research across diverse therapeutic areas.
SXR Laboratories maintains an active network of specialized subcontractors to recommend to our partner CRO companies. When our partners need specific expertise or additional capacity, they turn to us for qualified recommendations – and we want to recommend you.
We collect and maintain profiles of qualified subcontractors across all areas of clinical research. When our partner CROs have project needs that match your capabilities, we provide them with your company profile and contact information to initiate direct engagement.
Complete our brief registration form to add your company to our recommended subcontractor database. When opportunities match your profile, we’ll connect you directly with our partner CROs.
Complete our brief registration form to add your company to our recommended subcontractor database. When opportunities match your profile, we’ll connect you directly with our partner CROs.
Note: By registering, you agree to have your company information shared with SXR Laboratories’ partner CRO companies seeking subcontractor services. All business agreements are made directly between you and the contracting CRO.
Specialized areas where we engage qualified subcontractors
Site qualification, initiation, monitoring (on-site and remote), and close-out activities for clinical trials across all phases.
Central laboratory testing, biomarker analysis, pharmacokinetic studies, and specialized diagnostic services requiring niche expertise.
Protocols, clinical study reports, regulatory documents, medical monitoring letters, and publication support from experienced medical writers.
EDC build and validation, data review, query management, statistical programming, and TLF generation by qualified programmers.
Recruitment strategy development, digital marketing, patient advocacy engagement, and retention support for challenging studies.
IND/CTA submissions, regulatory dossier preparation, health authority interactions, and compliance assessments by regulatory experts.
To ensure quality standards, we require our subcontractors to meet these criteria
Documented quality management system compliant with ICH-GCP and applicable regulations
Appropriately trained and certified staff with documented
competencies
Adequate professional liability and business insurance coverage
Demonstrated experience and references in relevant therapeutic areas
Partner with us to bring your biomedical innovation to market faster. Our team of experts is ready to support your clinical research journey.