Local Touch

On A World Wide Scale

24/7 Availability

Our best specialists are ready to support you in preparation and conduct of your projects every day, including weekends and holidays.

Global Presence

ZM Company is a transcontinental CRO with offices in different parts of the world – North America (Canada, USA), Europe (Russia, France), and Asia (China).

Full-Service CRO Capabilities

Being on a global market since 2004, in partnership with other CRO’s, we offer full range of services from Feasibility to Clinical Study Report and are ready to address your specific needs.

Top Quality

Drug Safety CRO in Toronto

ZM Company is part of the Group of International Drug Safety Contract Research Organizations (CROs), with offices in Canada (ZM), Russia (3M Veritas), China (NJ YZ), and additional satellite offices in USA and EU.

Combining flexibility of small CRO with diverse experience, profound knowledge, 24/7 availability, variable resources of transcontinental company, and full-service CRO capabilities, we adhere to providing high quality creative expert solutions for the clients’ projects with maximum flexibility and premier focus on the clients’ interests.

We bridge the gap between clinical and data management aspects of the trials to ensure the medical accuracy and integrity of data. Our diverse team of specialists are experts with great experience in different areas of Pharmaceutical Industry on a global market.

Our Services

Safety Management

  • ICSR processing
  • SAE Reconciliation
  • Safety Database
  • SAE Narratives Preparation
  • CRF and Line-Listings Safety Review

Medical Monitoring

  • 24/7 coverage
  • DSMB Services
  • Safety Management Plan Development
  • Site and Study Team Medical Support
  • Medical Insight on Study Documents Development

Study Management

  • Project Management
  • Clinical Monitoring
  • Site and Study Team Support
  • Trial Document Handling
  • Site Management

Medical Writing

  • Study Abstracts
  • Protocols
  • Clinical Study Reports
  • Informed Consent Forms

CRF and Database Design

  • CRF Design and Development
  • CRF Completion Guidelines Development
  • Database Development
  • Database Lock
  • Database Archiving

Data Validation

  • CDISC Compliant Datasets and Documentation
  • Data Management Plan Development
  • Data Validation Plan Development
  • Automatic and Manual Data Validation
  • Query Management

Medical Coding

  • MedDRA Terms Coding
  • WHO Drug Terms Coding
  • Coding Consistency Review


  • SAS-programming
  • Protocol Design and Sampling
  • Statistical Analysis Plan
  • Statistical Analysis Report
  • Programming of Tables, Listings and Figures


  • Vendor Audits
  • ICH-GCP Compliance Audit
  • Site Audits
  • Study-Specific Audits
  • PV Audit

Internal and Project Documents Development

  • SOPs
  • WIs
  • Checklists
  • Study-related Documents
  • Regulatory Documents

Regulatory Inspection Preparation

  • Consulting
  • Audit Preparedness Assessment
  • CAPA
  • Liaison with RA
  • Internal Document Assessment

Regulatory and IRB/IEB Submissions

  • Clinical Trials
  • Post-Marketing Studies
  • Communication with RA
  • SMO responsibilities
  • IRB/IEB Submissions

In-house and Online Training Seminars

  • General
  • Specific
  • Custom-designed

Mentoring and Staff Development

  • General
  • Specific
  • Custom-designed

Project Design and Conduct

  • General
  • Specific
  • Custom-designed


  • English, Russian, Chinese (Mandarin)
  • Pre-Clinical Trial Documents
  • Clinical Trial Documents
  • Pharmacovigilance Documents

Suit the Action to the Word,

From Our Blog

Latest News / Updates

ZM Company 3M Veritas Nanjing YZ Clinical Trial & Consulting