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Can Biotech - BioPharma Portal and B2B Marketplace MMS Holdings Inc. is an ISO 9001:2000 Certified organization located in Canton, Michigan. We provide clinical development support, medical writing, clinical programming, biostatistics and regulatory affairs services to the pharmaceutical, biotechnology and medical device industry. Quality and commitment are the hallmarks of our success and every project we complete reflects our core values and principles.
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Analytical
Assay Development;  Chromatography;  ELISA Assay;  Electron Microscopy;  Electrophoresis;  FACS Analysis;  FISH Analysis;  Immunoassay;  IsoElectric Focus (IEF);  Microarray;  Spectrometry;  Spectrophotometer Analysis;  X-Ray Crystallography; 

Animal Services
Animal Biotechnology;  Animal Management;  Feed Management;  Safety/Testing; 

Antibody and Antigen Services
Antibody Characterization/Testing;  Antibody Conjugation;  Antibody Fab and F(Ab')2 Preparation;  Antibody Labeling;  Antibody Production;  Antibody Purification;  Antibody Quantification;  Antigen Production;  Antigen Purification; 

Basic Research
Cell Biology;  Custom Expression Systems;  Molecular Biology;  Molecular Immunology;  Virology; 

Cell/Tissue Culture
Blood and Serum Collection;  Cell Banking;  Cell Culture Production;  Cell Line Characterization;  Cell Sorting;  Immunohistochemistry Services;  Tissue Preparation;  Tissue Storage and Retrieval; 

Chemistry
Biochemistry;  Combinatorial Chemistry/Library Development;  Drug Synthesis;  Organic Chemical Synthesis; 

Clinical Research Organizations
Clinical Trial Recruitment;  Complete Clinical Trial Management;  Data Management and Biostatistics;  Medical Writing;  Pharmacogenomics;  Preclinical Development;  Project Management and Clinical Monitoring;  Regulatory;  Study Design and Development; 

Compliance
FDA-U.S.;  GCP;  GLP;  GMP;  HPB-Canada; 

Contract Research Organizations
Contract Manufacturing;  Contract Pharmaceutical;  Contract Research; 

Data Analysis and Management
Bioinformatics;  Biostatistics;  Protocol Design; 

Drug Development
Discovery;  Efficacy Studies;  Formulation;  Screening;  Synthesis;  Toxicology Studies; 

Genomics
Chromosome Mapping;  Cloning/Subcloning;  Functional Studies;  Gene Construction;  Gene Expression Studies;  Gene Sequencing;  Genotyping;  In-Situ Hybridization;  Karyotyping;  Pharmacogenomic Analysis; 

Health and Safety
Adverse Reaction Assessment;  Post-Market Survelliance;  Safety Assessment;  Safety Protocol Development; 

Information Technology
Custom Tools;  Data Analysis;  Graphics;  Software;  Statistical Analysis;  Structural Modeling; 

Manufacturing
Manufacturing, Clinical;  Manufacturing, Commercial;  Manufacturing, Preclinical;  Manufacturing, Product Registration; 

Packaging
Aerosol Filling;  Delivery System;  Design and Testing;  Encapsulation;  Sterile Filling;  Storage;  Syringe Filling;  Tableting; 

Product Marketing
Information Services;  Outcomes Research;  Phase IV trials; 

Peptide/Protein Services
Peptide Synthesis;  Protein Conjugation;  Protein Purification & Analysis;  Recombinant Protein Expression; 

Process Development
Analytical Methods;  Formulation;  Process Development;  Scale-up; 

Proteomics
Expression Proteomics;  Functional Proteomics;  Protein Analysis; 

Purification
DNA;  Protein;  RNA; 

Quality Assurance and Control
Cleaning and Monitoring;  Compliance Audits;  Equipment Validation;  Facilities Design/Construction;  ISO;  QA Development; 

Regulatory
Compliance;  Licensing;  Monitoring Clinical Trials;  Registration;  Regulatory Submissions; 

Sequencing
DNA;  Polypeptide;  RNA; 

Synthesis
DNA/RNA Synthesis;  Oligonucleotide Synthesis;  Peptide Synthesis;  cDNA Cloning/Synthesis; 

Validation and Studies
Analytical Validation;  Biological Analysis;  Chemical Analysis;  Dosage Form and Stability;  Manufacturing Validation Support;  Process Validation; 


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