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
- RMP/REMS
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
Biostatistics
- SAS-programming
- Protocol Design and Sampling
- Statistical Analysis Plan
- Statistical Analysis Report
- Programming of Tables, Listings and Figures
Audits
- 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
Translations
- English, Russian, Chinese (Mandarin)
- Pre-Clinical Trial Documents
- Clinical Trial Documents
- Pharmacovigilance Documents
From Our Blog
Latest News / Updates
Guidance to the pharmaceutical industry during the COVID-19 pandemic_updated news
Due to the current epidemiological situation, the issue of developing and implementing additional measures to ensure the safety of participants in current and planned clinical trials, as well as consumers …Read More »
WONDERFUL HOLIDAY SEASON AND HAPPY NEW YEAR
Pharmacovigilance Associate
Contract Research Organization Nanjing YZ Clinical Trials & Consulting Co., Ltd. within an international group of companies ZM CRO GROUP www.zmcro.cn, with long-term (more than 20 years) experience of successful cooperation with …Read More »
