
Outsourcing research and development (R&D) requires more than a transactional vendor—it demands a collaborative, technology-driven partnership backed by proven compliance and regulatory rigor.
MYCO2, a subsidiary of Singapore-listed LMS Compliance Ltd, partners with Dr. Can Bioscience (Hangzhou Deruikang) to provide full-service Contract Research Organisation (CRO) capabilities. We support pharmaceutical firms, biotechnology innovators, medical device developers, and academic research institutions worldwide.
By combining LMS Compliance Ltd’s regional testing framework with Dr. Can Bioscience’s specialized animal experiment center and technical laboratory infrastructure, MYCO2 bridges the gap between early scientific discovery and commercial viability.
Our non-standard biopharmaceutical research service platform delivers high-traceability, publication-ready data structured across eight dedicated technical service modules:
Standardized SPF-grade housing, specialized diet/environmental management, and long-term cohort maintenance for experimental animals.
Precision surgical modeling (e.g., spinal cord injury [SCI] models, cardiovascular ligation, tumor transplantation, and targeted organ interventions).
Standard routine, induced, and genetically engineered animal models across oncology, neurology, metabolic, and inflammatory disease categories.
High-precision enzymatic assays, metabolic marker profiling, tissue homogenate assays, and functional biomarker quantification.
Complete automated animal blood routine (CBC) panels, coagulation profiling, differential counts, and comprehensive urine chemistry testing.
Tissue fixation, paraffin/frozen sectioning, H&E staining, IHC (Immunohistochemistry), IF (Immunofluorescence), and qualitative/quantitative histopathological evaluation.
Target identification, gene expression profiling (qPCR/RT-PCR), Western Blot, ELISA, molecular cloning, and cell signal transduction assays.
Untargeted and targeted metabolomics profiling via LC-MS/GC-MS, coupled with advanced bioinformatic data processing, pathway analysis, and statistical visualization.
Understanding drug absorption, distribution, metabolism, and excretion (ADME) is vital for dose optimization. We conduct rigorous PK/PD evaluations in living systems to determine therapeutic windows and metabolic behavior.
Validate candidate safety prior to clinical trials. Our safety and toxicology assessments evaluate acute, sub-chronic, and organ-specific toxicity to align with international regulatory frameworks.
For sophisticated bio-technological research, our extended network utilizes cutting-edge analytical tools, including:
In Vivo Brain-Computer Interfaces (BCIs) for advanced neurological and neuromuscular studies.
3D Electron Microscopy & Micro-CT for high-resolution anatomical and structural visualization.
Multi-Omics Integration combining molecular data with docking simulations for precise biomarker discovery.
We ensure complete scientific integrity, transparent communication, and periodic progress updates throughout every phase of your project:
In-depth evaluation of your experimental objectives, target disease models, and regulatory targets.
Formalization of study scope, custom protocol design, milestone timelines, and technical deliverables.
Rigorous trial execution within certified research environments under strict quality assurance.
Multidimensional data synthesis, including raw datasets, bioinformatics reports, and publication-ready documentation.
Post-study consultations, long-term scientific support, and follow-up phase planning.
Supported by LMS Compliance Ltd, ensuring strong regional presence, financial stability, and robust quality control systems.
Integrated with Dr. Can Bioscience, giving access to established animal centers, disease models, and advanced analytical instrumentation.
From animal husbandry and surgical modeling to metabolomics profiling and bioinformatics data analysis.
Traceable, standardized documentation suitable for international market entry and scientific publishing.
Conveniently located to service clients across Malaysia, Singapore, China, ASEAN, and global markets.
Consult with our specialized CRO team to discuss your protocol requirements or request a customized proposal for your next preclinical project.